Dermoscopy The Essentials - Soyer - 2nd Ed - 2012
Dermoscopy The Essentials - Soyer - 2nd Ed - 2012
Dermoscopy The Essentials - Soyer - 2nd Ed - 2012
The Essentials
ERRNVPHGLFRVRUJ
Commissioning Editor: Russell Gabbedy
Development Editor: John Leonard
Project Manager: Cheryl Brant
Design: Kirsteen Wright
Marketing Manager(s) (UK/USA): Gaynor Jones/Helena Mutak
DERMOSCOPY
The Essentials SECOND EDITION
Giuseppe Argenziano, MD
Professor of Dermatology
Dermatology Unit
Medical Department
Arcispedale Santa Maria Nuova
Reggio Emilia
Italy
Rainer Hofmann-Wellenhof, MD
Professor of Dermatology
Department of Dermatology
Medical University of Graz
Graz
Austria
Iris Zalaudek, MD
Professor of Dermatology
Department of Dermatology
Medical University of Graz
Graz
Austria
ERRNVPHGLFRVRUJ
# 2012, Elsevier Limited. All rights reserved.
The right of Peter Soyer, Giuseppe Argenziano, Rainer Hofmann-Wellenhof, Iris Zalaudek to be
identified as author of this work has been asserted by him in accordance with the Copyright, Designs
and Patents Act 1988.
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Notices
Knowledge and best practice in this field are constantly changing. As new research and experience
broaden our understanding, changes in research methods, professional practices, or medical
treatment may become necessary.
Practitioners and researchers must always rely on their own experience and knowledge in
evaluating and using any information, methods, compounds, or experiments described herein. In
using such information or methods they should be mindful of their own safety and the safety of
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With respect to any drug or pharmaceutical products identified, readers are advised to check the
most current information provided (i) on procedures featured or (ii) by the manufacturer of each
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of administration, and contraindications. It is the responsibility of practitioners, relying on their own
experience and knowledge of their patients, to make diagnoses, to determine dosages and the best
treatment for each individual patient, and to take all appropriate safety precautions.
To the fullest extent of the law, neither the Publisher nor the authors, contributors, or editors,
assume any liability for any injury and/or damage to persons or property as a matter of products
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instructions, or ideas contained in the material herein.
ISBN: 978-0-7234-3592-1
Saunders
ISBN-13: 9780723435921
Printed in China
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Foreword
As a big fan of the first edition of Dermoscopy-The makes learning dermoscopy easy and intuitive. The
Essentials, I am honored to have the opportunity to accompanying brief, conversational and occasionally
write this brief forward to the new and improved light hearted narrative, makes for an easy and
second edition. I congratulate the authors for whom memorable read. Whether you are a dermoscopy
this project is an obvious labor of love. They have novice reading through the book from beginning to
succeeded in making a great book even better. I also end, or a more experienced dermoscopist jumping
congratulate you, the reader, for having settled upon from section to section and comparing your
such an intuitive and effective primer in your quest to assessment with those of the authors, the book is an
master dermoscopy. absolute joy.
At the time of its original printing in 2004, For the reader who has already accomplished some
Dermoscopy-The Essentials had relatively little mastery of dermoscopy, I know you will derive great
competition and, in the case of the United States pleasure from the quality of the enclosed images and
audience, a very limited market. In the intervening the insights of the authors. For the novice, I have to
years interest in dermoscopy has grown considerably. warn you that reading this book is the first step along
Diffusion of the use of dermoscopy into clinical a path to dependency. Once you have invested the
practice in the United States continues to lag time to become proficient in the use of dermoscopy,
somewhat behind that of Europe, but nevertheless it is you will no longer be satisfied with simple visual
now quite robust. Worldwide, there has been a rapid inspection. Your sense of both cognitive gratification
increase in dermoscopy associated publications both and clinical confidence will increasingly depend on
as it relates to original observations and teaching the application of this very simple yet so elegant
materials, but in this now more crowded landscape, technique.
Dermoscopy-The Essentials continues to stand out as an
especially valuable tutorial and reference.
I commend the authors of this volume for their use
of such a simple yet elegant and effective format. The Allan C. Halpern, MD MSc
traffic light visual tool coupled with the check box Chief, Dermatology Service
characterization of a large collection of some of the Memorial Sloan Kettering Cancer Center
best clinical and dermoscopic images in the literature, New York, New York USA
vii
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Preface to the First Edition
The authors of this book are on a quest. For years we lesions, green for low-risk lesions and orange for the
have been lecturing, creating articles, CDs and books gray-zone lesions. The associations between what you
with the goal of making dermoscopy, dermatoscopy, see with dermoscopy and the traffic light colors will
epiluminescence microscopy, ELM, skin surface sink into the recesses of your mind and come into play
microscopy, or whatever you choose to call the when you see similar dermoscopic criteria or patterns
technique, the standard of care for all dermatologists on your patients. You have to learn the basics;
and others who see patients with pigmented skin however, intuition and ‘gut’ feelings come into play
lesions. There are wonderful works already written in on a regular basis. Never ignore instinctive
the standard fashion that promote dermoscopy, yet in impressions.
some way they have not lit a fire in us all to joyfully We worked very well together as a team but it was
and relatively effortlessly learn a technique that spares not always easy, especially since the authors live on
tissue and saves lives. different continents and we face the typical trials and
If there are books that can teach languages such as tribulations of the human experience. However, we
German or Italian in ‘10 minutes a day’ why not create never lost sight of our goal and egos did not take hold.
a dermoscopy book that is ‘short and sweet’, ‘101’, fun This book is a work of love from doctors who are true
and easy to go through? The aim is to include images believers in a technique that is essential for our
that cover everything that is out there, not only in a patients. People’s fathers, mothers, sons, daughters,
university clinic but also in private practice, and with grandparents, aunts, and uncles entrust us with their
facts that are the essentials and more! health, their lives! We have the responsibility to be the
This is not a classic medical textbook and that is best that we can be to prevent the pain and suffering
intentional. For example, the ‘traffic lights’ are a tool that goes along with the most insidious of enemies,
for the busy practitioner to use to rapidly review the melanoma. Let dermoscopy be like the seat belt of
book over and over again, because one aspect of your car. You should never leave home without it.
mastering dermoscopy is the internalization of the
The Authors
basic principles. Look at the images, then look at the
colors of the traffic lights. Red indicates high-risk
ix
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Preface to the Second Edition
How time flies! It’s hard to believe that the first edition while to refine and update the content and, if relevant,
of Dermoscopy: The Essentials is now already seven years the illustrations. We specifically focused on this
old and so it is time for us to revamp our book; a task second goal with this new edition and have substituted
greeted with both enthusiasm and eagerness by our nearly 50% of the dermoscopic and clinical images
new author team. For this second edition we welcome and have unified all the annotations.
Dr Iris Zalaudek and we say goodbye to Drs Johr and We are especially indebted to the Elsevier Editorial
Scalvenzi. However, where we may be new in terms of Team, John Leonard and Russell Gabbedy, for their
the project at hand, we are old as colleagues and peers, highly professional support of our work and for being
having known each other for over 10 years (up to so flexible in the many small aspects intrinsic to
nearly 20 years in some cases), and having been publishing a book.
through many highs and lows together. Even though As with the first edition we consign our book to all
great distances separate us physically, through the use those interested in the science and art of dermoscopy
of modern technology and our own developed and hope that we contribute to the lofty goal of
strategies and procedures we continue to work together eradicating melanoma.
and collaborate, negating the physical distance from
each other to an impression of merely being next-door
to one another. In this modern age the physical H. Peter Soyer, Brisbane, Australia
distance of thousands of kilometers and eight to nine Giuseppe Argenziano, Reggio Emilia, Italy
different time zones are obstacles no longer. Rainer Hofmann-Wellenhof, Graz, Austria
The theory for a second edition is usually to Iris Zalaudek, Graz, Austria & Reggio Emilia, Italy
maintain the concept and design in general terms, 2011
xi
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Acknowledgements
To my Oz-based team, Zoja and Niko, for both To my teacher in dermoscopy and to my friends in the
their support and welcome distraction from field of dermoscopy. Special thanks go to my wife
my work. Andrea and my children Elisabeth, Paul, Martin and
H. Peter Soyer Georg, who have given me the strength to joyfully
work on the book.
To my mentor, my best friends and the love of my life, Rainer Hofmann-Wellenhof
all of whom are with me in this book. To my children,
Silvia and Gabriele, who are the most precious part To my "dermoscopy" family for their friendship, to
of my life. my parents Ilse and Gunter, my sister Karin and my
Giuseppe Argenziano niece Lilith for their love, and for the one representing
both families in my life.
Iris Zalaudek
xiii
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xiv
Introduction: The 3-point
checklist
The short, easy way to avoid missing a melanoma using
1
dermoscopy
Box 1.1 Other names for dermoscopy with pigmented skin lesions, there is a wide variety of
products to choose from.
Dermatoscopy
Epiluminescence microscopy (ELM)
The 3-point checklist
Skin surface microscopy
To encourage clinicians to start using dermoscopy,
simplified algorithms for analyzing what is seen with
Dermoscopy is an in vivo noninvasive diagnostic the technique have been developed.
technique that magnifies the skin in such a way that For the novice dermoscopist, the primary goal of
color and structure in the epidermis, dermoepidermal dermoscopy is to determine whether a suspicious
junction, and papillary dermis become visible. This lesion should be biopsied or excised. The bottom line
color and structure cannot be seen with the naked eye. is that no patient should leave the clinic with an
With training and experience, dermoscopy has been undiagnosed melanoma.
shown to significantly increase the clinical diagnosis For the general physician, dermoscopy can be used
of melanocytic, non-melanocytic, benign and to determine whether a suspicious lesion should be
malignant skin lesions, with a 10-27% improvement evaluated by a more experienced clinician.
in the diagnosis of melanoma compared to that Dermoscopy is not just for dermatologists; any
achieved by clinical examination alone. There is, clinician who is interested can master this potentially
however, a learning curve to mastering dermoscopy, life-saving technique.
and it is essential to spend time perfecting it—practice
makes perfect! Triage of suspicious pigmented skin lesions
The 3-point checklist was developed specifically for
novice dermoscopists with little training to help them not
Technique
to misdiagnose melanomas while improving their skills.
In classic dermoscopy, oil or fluid (mineral oil, Results of the 2001 Consensus Net Meeting on
immersion oil, KY jelly, alcohol, water) is placed over Dermoscopy (Argenziano G, J Am Acad Dermatol
the lesion to be examined. Fluid eliminates surface 2003) showed that the following three criteria were
light reflection and renders the stratum corneum especially important in distinguishing melanomas
transparent, allowing visualization of subsurface from other benign pigmented skin lesions:
colors and structures. Using handheld dermoscopes
• dermoscopic asymmetry of color and structure;
that exploit the properties of cross-polarized light
• atypical pigment network; and
(polarized dermoscopy), visualization of deep skin
• blue-white structures (a combination of the
structures can be achieved without the necessity of a
previous categories of blue-white veil and
liquid interface or direct skin contact with the
regression structures).
instrument.
The list of dermoscopy instrumentation is long and Statistical analysis showed that the presence of any
continues to grow and evolve with the development of two of these criteria indicates a high likelihood of
better and more sophisticated handheld instruments melanoma. Using the 3-point checklist, one can
and computer systems. Depending on the budget and have a sensitivity and specificity result comparable
goals for the evaluation and management of patients with other algorithms requiring much more
1
training. In a preliminary study of 231 clinically
DERMOSCOPY - The Essentials
Table 1.1 Definition of dermoscopic criteria for the
equivocal pigmented skin lesions, it was shown
3-point checklist. The presence of two or three
that, after a short introduction of 1-h duration,
criteria is suggestive of a suspicious lesion
six inexperienced dermoscopists were able to
classify 96.3% of melanomas correctly using this
3-Point checklist Definition
method.
This first chapter provides 60 examples of benign 1. Asymmetry Asymmetry of color and
and malignant pigmented skin lesions to demonstrate structure in one or two
how the 3-point checklist works and the practical perpendicular axes
value of this new and simplified diagnostic algorithm. 2. Atypical network Pigment network with
The 3-point checklist was designed to be used as a irregular holes and thick lines
screening method. The sensitivity is much higher than 3. Blue-white structures Any type of blue and/or white
the specificity to ensure that melanomas are not color
misdiagnosed. We recommend that all lesions with a
positive test (3-point checklist score of 2 or 3) are
excised.
2
1
Asymmetry
Atypical network
Blue-white structures
* Total score 3
*
*
Figure 1 Melanoma
Criteria to diagnose melanoma can be very subtle or obviously present as in this case. This lesion clearly
demonstrates all of the 3-point checklist criteria, namely, asymmetry in all axes, an atypical pigment
network (circle), and blue-white structures (asterisks).
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 0
Figure 2 Nevus
In contrast to Figure 1, none of the features of the 3-point checklist is seen in this lesion. The lesion is
symmetrical, and the pigment network is regular, although it might seem to be atypical because the line
segments are slightly thickened. Also there is no hint of any blue and/or white color.
3
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 3 Nevus
The novice might find this lesion difficult to diagnose. If in doubt, cut it out! With experience, the clinician
will excise fewer of these banal nevi. There is asymmetry; however, neither an atypical pigment network
nor subtle blue-white structures are present.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
Figure 4 Melanoma
Even for a beginner, the asymmetry of color and structure should be obvious. This asymmetrical lesion
also demonstrates blue-white structures (circle).
4
1
Asymmetry
Atypical network
Blue-white structures
Total score 3
Figure 5 Melanoma
The color and structure in the lower half is not a mirror image of the upper half; therefore, there is
asymmetry. An atypical pigment network with thickened and broken-up line segments (circle) and a large
area of blue-white structures (arrows) are also seen.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
Figure 6 Melanoma
This lesion is slightly asymmetric in shape and more in structure, and therefore, a red flag should be
raised. No pigment network is present, but there are numerous shiny white streaks (also called chrysalis-
like structures) (arrows) representing a variation on the theme of blue-white structures.
5
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 8 Nevus
Some melanomas are featureless, so beware! The color and structure in the right half of the lesion is not a
mirror image of the left half. The presence of irregular black dots in the left upper corner (circle) add to the
asymmetry. Pigment network and blue-white structures are not seen.
6
1
Asymmetry
Atypical network
Blue-white structures
Total score 0
Figure 9 Nevus
If in doubt, cut it out! With practice, fewer lesions that look like this will be excised. This is highly
symmetrical, and there is a great example of a regular pigment network in this banal nevus. Do not be
fooled by the dark central color—it is not always a sign of malignancy. No blue-white structures are seen.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 3
Figure 10 Melanoma
This lesion is a straightforward case of melanoma. The diagnostic criteria are striking, obvious asymmetry
of color and structure, a markedly atypical pigment network (arrows), and blue-white structures (circle).
7
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 11 Nevus
The clinical ABCDs could lead you astray with this banal nevus. There is asymmetry, but there is also a
typical pigment network and blue-white structures are absent.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
*
*
*
*
Figure 12 Melanoma
The yellowish globules seen here are not the multiple milia-like cysts of a seborrheic keratosis. They are
the ostia of appendages as seen only on head and neck lesions (arrows). There is slight asymmetry of
color and structure, and no pigment network is observed; however, blue-white structures are seen
throughout the lesion (asterisks).
8
1
Asymmetry
Atypical network
Blue-white structures
Total score 3
*
*
Figure 13 Melanoma
Clinicians might think that this lesion is nothing to worry about until they examine it with dermoscopy.
There is asymmetry of color and structure, an atypical pigment network and blue-white structures
(asterisks) cover part of the lesion.
Checklist
Asymmetry
Atypical network
* Blue-white structures
* Total score 2
*
*
Figure 14 Melanoma
The extensive blue-white structures (asterisks) are the first clue to the seriousness of this lesion.
Particularly color is clearly asymmetrical. A pigment network is absent, and there are well-developed
blue-white structures.
9
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 3
Figure 16 Melanoma
Asymmetry is unmistakably present in this lesion, but whether the pigment network is atypical in the right
upper corner (arrow) is debatable. Blue-white structures (circle) are clearly seen. There is no doubt that it
should be excised.
10
1
Asymmetry
Atypical network
Blue-white structures
Total score 2
Checklist
Asymmetry
Atypical network
* Blue-white structures
* * Total score 2
Figure 18 Melanoma
This lesion is clearly not benign. Is it, however, a basal cell carcinoma or melanoma? Once again, there is
significant asymmetry of color and structure with prominent blue-white structures (asterisks). It is difficult
to decide whether a pigment network is present or not (arrows).
11
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 19 Nevus
This stereotypical benign nevus is commonly seen when performing dermoscopy. The blotch of dark
brown color is not significant. Although there is slight asymmetry of color and structure, the lesion is
characterized by a typical pigment network and no clear-cut blue-white structures are seen.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
*
*
*
Figure 20 Nevus
The pattern of criteria shown here is most often seen with a Spitz nevus, but the differential diagnosis should
include Clark (dysplastic) nevus and melanoma. There is slight asymmetry of color and structure. A pigment
network is absent, with blue-white structures (asterisks). The checklist will not work for all lesions, and it is
important to take into account the history and age of the patient when deciding what to do.
12
1
Asymmetry
Atypical network
Blue-white structures
Total score 3
* *
*
Figure 21 Nevus
Another Spitz nevus-like pattern is demonstrated in this lesion, this time with hints of an atypical pigment
network (circle) and blue-white structures (asterisks).
Checklist
Asymmetry
* Atypical network
Blue-white structures
Total score 2
*
*
*
Figure 22 Melanoma
This banal clinical lesion has a strikingly worrisome dermoscopic appearance, with asymmetry of color
and structure. No pigment network is present, but blue-white structures are seen throughout the lesion
(asterisks).
13
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 23 Nevus
This lesion is benign. Compare it with the other lesions shown in this chapter with more obvious
asymmetry of color and structure, an atypical pigment network, and blue-white structures. There is slight
asymmetry of color and structure, although 100% symmetry is never found in nature. No pigment network
or blue-white structures are seen.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
*
*
*
Figure 24 Nevus
Two criteria of the 3-point checklist are present in this lesion, which should therefore be excised. There is
slight asymmetry and an atypical pigment network covering the left part of the lesion (asterisks).
14
1
Asymmetry
Atypical network
Blue-white structures
Total score 3
*
*
Figure 25 Melanoma
This is a clear-cut melanoma because of the striking asymmetry of color and structure, and the presence
of diffuse blue-white structures (asterisks). An atypical pigment network can be discerned in the right part
of the lesion (circle).
Checklist
Asymmetry
Atypical network
Blue-white structures
* * Total score 2
*
*
15
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 3
Figure 27 Melanoma
All three checklist criteria are seen in this lesion. There is significant asymmetry of color and structure with
a well-developed atypical pigment network (arrows). In the right lower part of the lesion, a blue-white
structure can be discerned (circle).
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
Figure 28 Melanoma
Significant asymmetry of color and structure is created by blue-white structures (arrows), which occupy
most of the lesion. An atypical pigment network is not seen.
16
1
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 29 Nevus
Only one of the checklist criteria is present in this lesion, so this lesion is benign. The lower half of the
lesion does not mirror the upper half, thereby displaying subtle asymmetry. No pigment network or blue-
white structures are seen.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 30 Nevus
The presence of a single criterion from the checklist is usually not sufficient to diagnose malignancy. Note
the asymmetry of color and structure—the left side of the lesion is not a mirror image of the right side. An
atypical pigment network and blue-white structures are absent.
17
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
*
*
Figure 31 Nevus
This is a difficult lesion to interpret. Although only one criterion of the 3-point checklist is present, the
overall appearance may raise some suspicion that it could be a melanoma. The lesion is symmetrical and
there is no pigment network. In the center, blue-white structures are so slight that they might be difficult to
detect (asterisks).
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 3
Figure 32 Melanoma
All criteria of the 3-point checklist are present, underlining the impression that this lesion is a melanoma.
Although the contour is symmetrical, there is asymmetry of color and structure within. A clear-cut
thickened pigment network (arrows) is present, with small foci of blue-white structures (circles) in the
center of the lesion. This early melanoma might go undiagnosed if dermoscopy is not used.
18
1
Asymmetry
Atypical network
Blue-white structures
Total score 3
*
*
*
Figure 33 Melanoma
Once again, all three features of the checklist are clearly present and even a novice dermoscopist should
immediately suspect a melanoma. There is striking asymmetry of color and structure with zones
displaying an atypical pigment network (arrow). There are also clear-cut areas with another variation on
the theme of blue-white structures, namely, peppering (asterisks).
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
19
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
*
* *
*
*
Figure 35 Nevus
Despite the significant asymmetry of color and structure, this lesion is benign. There is no hint of a
pigment network, but blue-white structures are present (asterisks). With a score of 2, excise this lesion or
show it to a more experienced dermoscopist.
Checklist
Asymmetry
Atypical network
Blue-white structures
* Total score 3
Figure 36 Nevus
This is a difficult lesion to diagnose because all three features are very subtle. There is an atypical pigment
network on the left side (arrow) and globules (circle) on the right side; it is therefore an asymmetrical
lesion. Blue-white structures (asterisks) can also be seen throughout.
20
1
Asymmetry
Atypical network
* Blue-white structures
Total score 1
Figure 37 Nevus
This is a slightly asymmetrical lesion with a typical pigment network. Do not confuse the multifocal
hypopigmentation (asterisks) with the white color that can be seen in blue-white structures.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 3
Figure 38 Melanoma
Thin melanomas commonly exhibit all three checklist criteria, as demonstrated by this example. There is
asymmetry of color and structure with a few foci (arrows) of an atypical pigment network. In the center, an
area of blue-white structures is also seen (asterisk). The dermoscopic differential diagnosis includes
severely dysplastic nevus and in situ melanoma.
21
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
* Total score 2
* *
Figure 39 Melanoma
This dark lesion is a cause for concern. Note the shape asymmetry and multiple anastomosing blue-white
structures throughout the lesion (asterisks). With two out of three well-developed criteria present, this
melanoma will not be misdiagnosed if the 3-point checklist is used.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 0
Figure 40 Nevus
There is an obvious lack of striking criteria in this lesion compared to the melanomas already seen in this
chapter. An atypical pigment network and blue-white structures are not seen.
22
1
Asymmetry
Atypical network
Blue-white structures
Total score 3
*
*
Figure 41 Melanoma
This is a clear-cut example of a melanoma with a checklist score of 3. There is striking asymmetry of color
and structure. Several zones exhibit variations of the morphology of an atypical pigment network (arrows).
In paracentral location, blue-white structures can be clearly seen (asterisks). Always concentrate and
focus attention to identify important criteria that might be present in a lesion.
Checklist
Asymmetry
Atypical network
* Blue-white structures
Total score 1
*
*
Figure 42 Nevus
Numerous foci of blue-white structures are seen throughout (asterisks). An atypical pigment network is not
seen. Even though the score is only 1, the dark color and blue-white structures are worrisome. Although it
turned out to be a low-risk nevus, it is better to err on the side of safety and remove these borderline lesions.
With experience, fewer pigmented skin lesions that look like this will be removed.
23
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
* Total score 1
* *
Figure 43 Nevus
A score of 2 can be achieved for this lesion only if it is considered to be asymmetrical. This image is
similar to Figure 42. The pigment network is typical and is therefore not scored. There are, however,
numerous foci of blue-white structures (asterisks).
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
*
*
*
24
1
Asymmetry
* Atypical network
Blue-white structures
* Total score 1
Figure 45 Nevus
This lesion has a 3-point checklist score of 1. It is relatively symmetrical and there is no pigment network.
Blue-white structures (asterisks), in this instance only whitish, are clearly visible. This example can be a
potential pitfall for the 3-point checklist because nodular basal cell carcinomas can mimic dermal nevi
dermoscopically, particularly when the vascular structures are not carefully examined.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 46 Nevus
This is another lesion difficult to diagnose for the beginner because its checklist score may be 1 or 2.
Always remember: if a lesion could be high risk, excise it or follow the patient closely. There is slight
asymmetry of dermoscopic structures (globules) but no pigment network. Very subtle whitish areas may
be interpreted as blue-white structures.
25
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 47 Nevus
The checklist score for this lesion is only 1, with slight asymmetry of color and structure.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
Figure 48 Nevus
This lesion is easy to handle from a management point of view because two of the three checklist criteria
are present, so it should be excised. There is noticeable asymmetry of color and structure, and an atypical
pigment network is found in the left upper half of the lesion. No blue-white structures are seen.
26
1
Asymmetry
Atypical network
Blue-white structures
Total score 2
Figure 49 Nevus
This dermoscopic image is worrisome, showing two of the three checklist criteria. There is asymmetry of
color and structure and foci of an atypical thickened and branched pigment network (arrows). The novice
should excise a lesion with this dermoscopic appearance, although the pathology report might not detect
any high risk.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 50 Nevus
This is a blue nevus for which the checklist score is obviously 1. This lesion is symmetrical, without a
pigment network, but blue-white structures are seen homogeneously throughout the lesion. The
dermoscopic appearance of blue nevi is unique, but always be cautious when making the diagnosis
because rarely nodular melanoma and cutaneous metastatic melanoma mimic a blue nevus.
27
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
Figure 51 Nevus
Again, the management of this lesion after evaluating it with the 3-point checklist is straightforward. With a
score of 2, this could be a high-risk lesion. There is striking asymmetry of shape and structure. An atypical
pigment network is observed throughout the periphery of the lesion. No blue-white structures are seen.
The discordance between the positive 3-point checklist score and pathology is well known for this type of
nevus, which is also called black nevus.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 52 Nevus
In contrast to the lesion above, the checklist score for this nevus is just 1. There is no significant
asymmetry of structure with only delicate foci of blue-white structures in the centre of the lesion. No
atypical pigment network can be discerned.
28
1
Asymmetry
Atypical network
Blue-white structures
Total score 2
Figure 53 Nevus
This lesion also has a checklist score of 2. This example shows the limitations of the 3-point checklist.
There is asymmetry because the lower half does not mirror the upper half. Also note that the pigment
network is atypical (arrows). Blue-white structures are not observed.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 1
Figure 54 Nevus
This lesion is asymmetrical because the left side is not a mirror image of the right side. The line segments
of the pigment network are not thick, dark, or branched; therefore, it is not atypical. Do not confuse the
central hypopigmentation (asterisk) with blue-white structures.
29
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
*
*
*
Figure 55 Melanoma
There are two strikingly positive features present here—asymmetry and blue-white structures. Because
there are also a few satellite lesions (circle), it should be excised with high priority. Clear-cut asymmetry of
shape and structure and conspicuous blue-white structures (asterisks) are seen throughout the lesion. No
pigment network is seen, not even at the periphery.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
Figure 56 Nevus
The atypical pigment network (circle) in this asymmetrical lesion is worrisome, and the lesion should be
excised. No blue-white structures are seen. Although the histology was benign, this dermoscopic picture
might also be seen in in situ melanoma.
30
1
Asymmetry
Atypical network
Blue-white structures
Total score 2
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
Figure 58 Nevus
Two of the 3-point checklist criteria are present. Asymmetry of color and shape is evident, and centrally
located blue-white structures (circle) are seen. Because of a 3-point checklist score of 2, excision of this
lesion is recommended.
31
DERMOSCOPY - The Essentials
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 0
Figure 59 Nevus
The checklist score for this lesion is zero.
Checklist
Asymmetry
Atypical network
Blue-white structures
Total score 2
32
Pattern analysis
Dermoscopic criteria for specific diagnoses
2
Dermoscopic analysis of pigmented skin lesions is or gray. Modifications of the pigment network vary
based on four algorithms: with changes in the biologic behavior of melanocytic
skin lesions, and these variations therefore merit
• pattern analysis;
special attention.
• the ABCD rule;
• Menzies’ 11-point checklist; and
• the 7-point checklist Globular pattern
Variously sized, round to oval brown structures fill
The common denominator of all these diagnostic
these melanocytic lesions. This pattern can be found
algorithms is the identification and analysis of
in congenital and acquired melanocytic and Clark
dermoscopic criteria found in the lesions. The
(dysplastic) nevi.
majority of the dermatologists who participated in the
second consensus meeting were proponents of pattern
analysis. The basic principle is that pigmented skin Homogeneous pattern
lesions are characterized by global patterns and This pattern is characterized by a diffuse, uniform,
combinations of local criteria. structureless color filling most of the lesion. Colors
include black, brown, gray, blue, white, or red.
A predominantly bluish color is the morphologic
Four global dermoscopic patterns for hallmark of blue nevi.
melanocytic nevi
Reticular pattern Starburst pattern
The reticular pattern is the most common global The starburst pattern is characterized by the presence
pattern in melanocytic lesions. It is characterized by a of pigmented streaks and/or dots and globules in a
pigment network covering most parts of a lesion. The radial arrangement at the periphery of a melanocytic
pigment network appears as a grid of line segments lesion. This pattern is the stereotypical morphology in
(honeycomb-like) in different shades of black, brown, Spitz nevi.
33
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 61 Nevus
The reticular type is probably the most common dermoscopic feature of a flat acquired melanocytic
nevus. It is characterized by a typical pigment network that fades out at the periphery. There are also a
few small islands of hypopigmentation—a common finding in benign nevi. The histopathologic distinction
between a junctional nevus and a compound nevus is commonly given, but the distinction cannot always
be made dermoscopically. Moreover, it is clinically irrelevant.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 62 Nevus
Here is another example of the morphology seen with the reticular type of banal nevus. The quality of the
typical pigment network demonstrates darker and thicker lines. The benign nature of this lesion is
emphasized by the fading out at the periphery of the pigment network.
34
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
*
* *
Figure 63 Nevus
This is a reticular-type lesion with a few dots. In the center of the lesion, the lines of the pigment network
are slightly thicker and more heavily pigmented (circle). In addition, there are a few dark-brown dots
(arrows) and a hint of a blue-white structure (asterisks). Again, note the fading out of the pigment network
along the entire periphery of the lesion representing an important clue that this is a benign melanocytic
lesion. This can also be called a Clark, dysplastic, or atypical nevus; it is not a melanoma.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 64 Nevus
This lesion is characterized by a typical pigment network and numerous dots, which are situated on the
crossing points of the network lines. In the background, diffuse blue-white structures can be seen
covering most of the lesion. Histopathologically, the diffuse blue-white structures represent a dense
infiltrate of melanophages in the papillary dermis. The differentiation between a junctional and a
compound nevus is not possible dermoscopically.
35
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 65 Nevus
A reticular-homogeneous pattern, as seen here, can be seen in banal nevi. In the center, there is homogeneous
black pigmentation (black lamella), and at the periphery there is an annular distribution of a typical pigment
network. Once again, the pigment network fades at the periphery—a sign of a benign nature. If this was a solitary
lesion, in situ melanoma would be the differential diagnosis. Most people with this dermoscopic appearance
have multiple similar-appearing nevi, favoring low-risk pathology. Tape stripping can peel away the black lamella
and allows one to see whether there are any underlying typical or atypical structures.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 66 Nevus
The unusual type of reticular-homogeneous pattern seen here is more often found in younger pediatric
patients. In the center of the lesion, there is homogeneous hypopigmentation (not to be confused with the
bony-milky white color of regression), and this is surrounded by a small rim of pigment network. The lines
of the pigment network are thickened and the meshes are slightly irregular. The overall architecture of the
network, however, is symmetrical and regular.
36
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 67 Nevus
A stereotypical reticular pattern is seen here. The pigment network is typical, but unevenly distributed and
fades out at the periphery. In addition, there are hypopigmented areas throughout the lesion (arrows). This
nevus does not reveal criteria used to diagnose melanoma (melanoma-specific criteria). Because of the
uneven distribution of the pigment network and variations in the shades of brown, the novice
dermoscopist should consider excision or close dermoscopic and clinical follow-up.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 68 Nevus
The patchy reticular pattern shown here is associated with an uneven distribution of a typical pigment
network. The intensity of pigmentation of the lines alternates, giving this pigment network a patchy
appearance, and is similar to Figure 67. The general principle to remember is that any unevenness of
relatively regular-appearing criteria is a minor cause for concern.
37
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
* *
Starburst pattern
Figure 69 Nevus
This nevus shows a variation of reticular-pattern morphology. Note the zone of homogeneous
hypopigmentation (asterisks) in the center. This is not an area of regression that would be seen in
melanoma. It is not bony-milky white.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 70 Nevus
This dermoscopic picture is very worrying. The reticular pattern with eccentric hyperpigmentation
dermoscopically simulates in situ melanoma arising in a pre-existing nevus. The upper right half of this
lesion is characterized by a slightly atypical pigment network (arrows). On the left lower side, there is an
area of homogeneous hypopigmentation with a few foci of delicate pigmentation commonly seen in
benign nevi. Do not hesitate to excise a lesion that looks like this as soon as possible. The final
histopathologic diagnosis is in situ melanoma within a pre-existing nevus in 10% of similar-appearing
lesions. In this case, the diagnosis was Clark (dysplastic) nevus, compound type.
38
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 71 Nevus
This is a rather unusual combined nevus, with a dome-shaped globular nevus on the lower left site and
a variation on the theme of a flat reticular nevus on the upper right site. This lesion should undoubtedly be
excised because the differential diagnosis represents a hypomelanotic nodular melanoma arising within
a superficial melanoma or a pre-existing dysplastic (Clark) nevus. However, this lesion turned out to be a
dysplastic (Clark) nevus adjacent to a benign dermal nevus.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 72 Nevus
This predominantly reticular pattern with a few small globules centrally is commonly observed in benign
nevi. The unusual aspect of this lesion is the finger-like projection at 2 o’clock (arrows) characterized by a
broken-up pigment network intermingled with some globules. This lesion was excised and
histopathologically diagnosed as dysplastic (Clark) nevus, compound type.
39
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 73 Nevus
This light-brown pinkish lesion reveals a central hypopigmented homogeneous area surrounded by a
subtle, not very pronounced pigment network in a ring-like fashion. The unusual aspect of this lesion is its
pinkish color, and in the absence of any history of growth, annual follow-up is the management approach
we choose for this patient.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 74 Nevus
This lesion can be regarded as a typical example of a reticular melanocytic proliferation. There is a central
zone of hyperpigmentation. The pigment network has rather regular qualities throughout the lesion.
However, it does not thin out nicely along the periphery as commonly observed in reticular nevi. Because
of this dermoscopic finding and heavy pigmentation, this is potentially a high-risk lesion.
Histopathologically, this was diagnosed as a junctional type of dysplastic (Clark) nevus. Novice
dermoscopists should not hesitate to excise lesions that look like this.
40
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 75 Nevus
This is another example of a reticular-homogeneous nevus with an annular reticular pattern in the
periphery and large central homogeneous hypopigmented area. The color of the hypopigmented area is
not bony-white as observed in regressive melanoma, and because of the overall symmetry of this lesion,
annual follow-up can be advised confidently by the novice dermoscopist.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 76 Nevus
This lesion has a uniform reticular pattern with only a delicate focus of paracentral hyperpigmentation
(circle). The pigment network is typical and slightly fades out at the periphery. The overall shape of the
lesion, however, is a bit asymmetric and lesions like this one should always be followed up.
41
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
*
*
Figure 77 Nevus
This is another example of the variation of morphology with the reticular pattern. In contrast to Figure 76,
the pigment network here is mostly atypical with a tendency to stop abruptly at the periphery (arrows).
Central hyperpigmented areas (asterisks) are also seen. This dysplastic (Clark) nevus simulates in situ
melanoma and should be excised.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 78 Nevus
This is a predominantly reticular type of nevus with a pigment network fading out nicely at the periphery.
In our opinion, this is the most common type of benign nevus in men. Still, as a rule, we do recommend
annual follow-up and self-monitoring of reticular nevi.
42
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 79 Nevus
This shows a stereotypical globular pattern of a benign nevus. There are numerous dots and globules of
similar shape and varying size throughout the lesion. No melanoma-specific dermoscopic criteria are
seen. This pattern is most commonly seen in adolescents but can also be found in adults. The
histopathology could show a junctional or compound nevus.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 80 Nevus
This shows one of the many variations of the morphology seen with the globular pattern. The most
relevant aspect of this lesion is the even distribution of closely packed, similar-appearing dots and
globules. In addition, there are a few milia-like cysts in the center of the lesion (arrows). Milia-like cysts are
not seen only in seborrheic keratosis.
43
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 81 Nevus
This globular pattern shows dots and globules that are not closely packed together, are similar in size and
shape, and have a slightly uneven distribution. No melanoma-specific criteria are seen in this banal lesion.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 82 Nevus
Most of this lesion is characterized by homogeneous light-brown pigmentation and subtle dots and
globules (arrows).
44
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 83 Nevus
This image shows a more worrisome variation of the globular pattern. Numerous dots and globules are
unevenly distributed throughout the lesion (circle) and vary in size and shape.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 84 Nevus
Here is another globular type of nevus. Numerous light-brown to blue-gray dots and globules, which are
of similar size and shape, are distributed regularly throughout the lesion. The only worrisome area is a
collection of about 15-20 gray globules (circle), which prompted the excision of this compound type of
Clark (dysplastic) nevus. Study lesions carefully to look for subtle yet potentially high-risk criteria.
45
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 85 Nevus
This is another stereotypical example of the globular pattern of nevus, in which the globules are very easy
to see. In the center of this lesion, numerous dark-brown dots and globules with a rectangular shape
(cobblestone-like) are present and are surrounded by a rim of brown pigmentation. Dermoscopically, this
lesion gives the impression of a papillomatous or raised character. Histopathologic examination revealed
a compound nevus.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 86 Nevus
The globular pattern seen here is similar to that in Figure 85, yet the globules are not that easy to see. The
lesion is composed of closely packed gray dots and globules. No other dermoscopic criteria are
observed. The variation of the color might alarm the inexperienced dermoscopist. Remember, if in doubt,
cut it out. This was a benign nevus. After seeing and excising a few lesions with this dermoscopic
appearance, the dermoscopist will feel more comfortable about not excising lesions that look like this.
46
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 87 Nevus
This lesion shows again a globular pattern. It contains numerous brown to gray globules, which are evenly
distributed throughout the lesion. The gray globules are situated predominantly in the center of the lesion
and correspond to nests of pigmented nevus cells in the papillary dermis. Remarkably, globular nevi
represent the stereotypical nevus subtype among children and teenagers.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 88 Nevus
It is amazing to see the many different variations on the theme of globular nevi. In the previous pages,
we have seen quite a few benign globular nevi, but all are morphologically different and unique.
The striking aspect of this uniformly pigmented globular nevus is its dark brown pigmentation. We are
happy to follow this nevus and recommend self-monitoring.
47
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 89 Nevus
This globular nevus raises at least the orange flag because the globules composing this lesion vary in size,
shape, and color and are also slightly unevenly distributed throughout the lesion. Because there was also
a concern from the patient in regard with this lesion, a deep shave biopsy was performed. The final
histopathologic diagnosis was a compound type of dysplastic (Clark) nevus.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 90 Nevus
Numerous irregularly sized brownish dots and globules are seen throughout this lesion. Although it is
very small, the dermoscopic asymmetry is striking. The pinkish color is an important clue that this could
be a high-risk lesion. Because of its high-risk appearance, a lesion like this one warrants a second
histopathologic opinion if it is signed out as a benign nevus as was the case here.
48
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 91 Nevus
One has to look carefully to recognize that this heavily pigmented nevus reveals a globular and not a
homogeneous pattern in its central part. The lighter pigmented peripheral ring displays a pattern
reminiscent of globules and reticulated lines telling us that in morphology there is always an overlap of
features. We were confident that this lesion was a variation on the theme of a benign globular nevus and
recommended annual follow-up and self-monitoring.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 92 Nevus
In some instances, the distinction between a globular and a reticular nevus is not that easy, as evidenced
by this irregularly outlined lesion. In the central parts, a pigment network characterized by thickened lines
and small holes prevail, whereas toward the periphery, a more globular pattern becomes evident.
Although we are raising the orange flag here, we felt confident that this lesion requires only follow-up.
49
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 93 Nevus
This lesion is characterized by diffuse homogeneous pigmentation. There is a subtle rim of
radially oriented line segments at the periphery, which represent streaks (arrows), and blue-white
structures in the center (circle). The dermoscopic differential diagnosis includes Clark (dysplastic) nevus
and Spitz nevus.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 94 Nevus
Apart from the blue-white structures and tiny dots in the central part (circle), this lesion displays a rather
uniform subtle reticular pattern, which made us comfortable to follow up this lesion. We are well aware
that some colleagues would prefer to excise a lesion like this one for peace of mind. Also the clinical
image was reassuring for us that we were dealing with a nevus.
50
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 95 Nevus
This lesion is characterized by a reticular-homogeneous pattern. Please note the focus of atypical
pigment network (circle). In addition, the left lower part of the lesion exhibits blue-white structures, and
these two signs are sufficient to warrant excision. In the realm of dysplastic (Clark) nevus, it is difficult to
determine whether a lesion is low or high risk dermoscopically; therefore, the novice is best advised to
excise gray-zone lesions as this one.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 96 Nevus
This is another example of a benign globular nevus with globules slightly varying in size, shape, and
coloration. Despite the irregular outline of this lesion, no action but follow-up has to be undertaken.
51
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 97 Nevus
This is a rather commonly observed variation of the theme of a reticular type of nevus. These lesions are
frequently found in adults. We judge this pigment network as typical and rather uniformly distributed. It is
fading out particularly in the lower right part of the lesion. Without any specific history, we were happy
with follow-up of this nevus and, in addition, recommended self-monitoring.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Figure 98 Nevus
This lesion is a variation of the homogeneous-reticular type of nevus reminiscent of a so-called black
nevus. Multiple jet-black homogeneous zones are seen at the periphery. Use tape stripping for this black
lesion mimicking in situ melanoma.
52
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
* Globular pattern
Homogeneous pattern
* * Starburst pattern
Figure 99 Nevus
This is a dome-shaped melanocytic nevus that reveals a subtle globular pattern with numerous light-
brown dots and globules throughout. Multiple blood vessels with dotted (asterisks) and comma-like
appearances (arrows) are seen. There are also a few milia-like cysts (circles), but this is not a seborrheic
keratosis. Clinically this lesion could be confused with a basal cell carcinoma, but the vessels in a basal
cell carcinoma are thick and branched (arborizing) and there would be no yellow color.
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
53
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
* Starburst pattern
54
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
*
*
55
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
* Homogeneous pattern
*
Starburst pattern
56
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
* Starburst pattern
*
*
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
57
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
* Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
58
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
59
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
*
* *
60
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
* Starburst pattern
*
* *
61
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
62
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
63
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
64
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
65
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
*
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
66
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
67
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
68
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
* Homogeneous pattern
* Starburst pattern
70
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
72
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
73
DERMOSCOPY - The Essentials
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
74
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
76
2
Pattern analysis
Four global patterns
for melanocytic nevi
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
Reticular pattern
Globular pattern
Homogeneous pattern
Starburst pattern
78
2
Pattern analysis
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
1
* 2
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
79
DERMOSCOPY - The Essentials
Five melanoma-
specific local criteria
Atypical network
* Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Pattern analysis
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
81
DERMOSCOPY - The Essentials
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
1 Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
2
Blue-white structures
3
82
2
Pattern analysis
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
3 Irregular blotches
* 4 Blue-white structures
1
2
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
* Irregular dots/globules
* Irregular blotches
Blue-white structures
Pattern analysis
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
1 * * Irregular dots/globules
Irregular blotches
2
Blue-white structures
3
85
DERMOSCOPY - The Essentials
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
86
2
Pattern analysis
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
87
DERMOSCOPY - The Essentials
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
*
Irregular dots/globules
Irregular blotches
* Blue-white structures
*
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
88
2
Pattern analysis
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
*
Atypical network
* Irregular streaks
Irregular dots/globules
* Irregular blotches
Blue-white structures
89
DERMOSCOPY - The Essentials
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
90
2
Pattern analysis
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
* Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
91
DERMOSCOPY - The Essentials
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
Five melanoma-
specific local criteria
Atypical network
Irregular streaks
Irregular dots/globules
Irregular blotches
Blue-white structures
92
2
Diagnosis of facial melanoma using Asymmetrically pigmented follicles
Pattern analysis
four site-specific melanoma-specific Asymmetrically pigmented follicles are gray circles/
criteria rings of pigmentation distributed asymmetrically
Facial melanomas usually occur in severely sun- around follicular ostia. Sometimes, the gray circles
damaged skin and is called lentigo maligna when an may contain an inner gray dot or circle.
in situ lesion, and lentigo maligna melanoma when
the lesion is invasive. Because of the specific anatomy
of facial skin characterized by numerous folliculo- Rhomboidal structures
sebaceous units and an effaced epidermis, melanomas Rhomboid structures are thickened areas of
on facial skin reveal the following dermoscopic pigmentation surrounding the follicular ostia with a
features. These criteria are present in facial melanomas rhomboidal appearance (a rhomboid is a
in various combinations and as a rule are not found in parallelogram with unequal angles and sides).
non-facial melanomas.
Gray pseudonetwork
Annular-granular structures Gray pseudonetwork describes gray pigmentation
Annular-granular structures are multiple brown or surrounding the follicular ostia formed by the
blue-gray dots surrounding the follicular ostia with an confluence of annular-granular structures.
annular-granular appearance.
93
DERMOSCOPY - The Essentials
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
Pattern analysis
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
95
DERMOSCOPY - The Essentials
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
96
2
Pattern analysis
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
Gray pseudonetwork
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
98
2
Pattern analysis
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
Four site-specific
melanoma-specific
criteria
Annular-granular
structures
Asymmetrically
pigmented follicles
Rhomboidal structures
Gray pseudonetwork
100
2
Pattern analysis
Four patterns for
acral melanocytic
lesions
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
101
DERMOSCOPY - The Essentials Four patterns for
acral melanocytic
lesions
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Pattern analysis
Four patterns for
acral melanocytic
lesions
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
104
2
Pattern analysis
Four patterns for
acral melanocytic
lesions
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Parallel furrow
Parallel ridge
Lattice-like
Fibrillar
Pattern analysis
melanocytic lesions but they can also be seen in papillomatous dermal
nevi, and rarely a few milia-like cysts are seen in
To diagnose non-melanocytic pigmented skin lesions,
melanomas.
there should be an absence of criteria for melanocytic
lesions (pigment network, globules, streaks,
Comedo-like openings
homogeneous and parallel patterns) and the presence
of criteria considered specific for basal cell carcinoma, Comedo-like openings refer to brownish-yellow or
seborrheic keratosis, hemangioma, or brown-black, irregularly shaped, sharply
dermatofibroma. circumscribed structures. Histopathologically, they
represent keratin plugs within dilated follicular
Blue-gray blotches openings. Due to oxidation of the keratinous
material, they often have a yellowish-brown or dark-
Blue-gray blotches are structureless areas that are brown to black color. Comedo-like openings are
round to oval and often irregular in shape. The color found predominantly in seborrheic keratoses, but they
ranges from brownish-gray to blue-gray. can also be seen in papillomatous dermal nevi.
Histopathologically they represent heavily pigmented, At times it is difficult to differentiate dark comedo-like
solid aggregations of basaloid cells in the papillary openings from the globules seen in melanocytic
dermis of superficial or nodular basal cell carcinoma. lesions.
Blue-gray blotches are a pathognomonic finding in
pigmented basal cell carcinoma, especially when Red-blue lacunae
associated with arborizing vessels and an absence of
Red lacunae appear as sharply demarcated, round to
criteria seen in melanocytic lesions.
oval structures. The color can vary from red, red-blue,
dark-red to black. A whitish color is also often seen in
Arborizing vessels vascular lesions. Histopathologically, red lacunae
Arborizing vessels are discrete, thickened, and represent dilated vascular spaces located in the upper
branched red blood vessels that are similar in dermis. Lacunae with dark-red to black color represent
appearance to the branches of a tree. vascular spaces that are partially or completely
Histopathologically they represent dilated arterial thrombosed. Red lacunae are the stereotypical
circulation that feeds the tumor. Arborizing vessels are criterion of hemangiomas and angiokeratomas.
99% diagnostic of basal cell carcinoma. Rarely they Structures similar in appearance can also be seen in
can be found in intradermal nevi or featureless subungual and subcorneal hematomas.
melanomas.
Central white patch
Milia-like cysts The central white patch diagnostic of
Milia-like cysts are variously sized, white or yellowish, dermatofibromas is a well-circumscribed, round-to-
round structures. Histopathologically, they represent oval, sometimes irregularly outlined, bony-milky-
intraepidermal horn globules, also called horn white area usually in the center of a firm lesion.
pseudocysts, a common histopathologic finding in There are many variations of the morphology of this
acanthotic seborrheic keratosis. Multiple milia-like criterion.
107
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
108
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
109
DERMOSCOPY - The Essentials Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
110
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
* Central white patch
111
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
* Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
* Red-blue lacunae
112
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Arborizing vessels
* Milia-like cysts
Comedo-like openings
Red-blue lacunae
113
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Pattern analysis
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
* *
* Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
115
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
116
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
117
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
118
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
119
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
*
Milia-like cysts
Comedo-like openings
* Red-blue lacunae
*
Figure 226 Seborrheic keratosis
Opaque color, milia-like cysts (asterisks), and comedo-like openings (arrows) are seen in this lesion with a
verrucous surface (circle). This lesion should prove easy to diagnose dermoscopically as a seborrheic
keratosis by now.
120
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
121
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
122
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
124
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
125
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
126
2
Six criteria for
Pattern analysis
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
* Comedo-like openings
* Red-blue lacunae
128
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
* Red-blue lacunae
*
Central white patch
129
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
* Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
131
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
133
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
* Comedo-like openings
*
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
134
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
* Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
135
DERMOSCOPY - The Essentials
Six criteria for
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
*
non-melanocytic
lesions
Blue-gray blotches
Arborizing vessels
* Milia-like cysts
Comedo-like openings
Red-blue lacunae
136
2
Pattern analysis
Six criteria for
non-melanocytic
lesions
* Blue-gray blotches
Arborizing vessels
Milia-like cysts
* Comedo-like openings
Red-blue lacunae
Blue-gray blotches
Arborizing vessels
Milia-like cysts
Comedo-like openings
Red-blue lacunae
139
DERMOSCOPY - The Essentials
140
3
141
DERMOSCOPY - The Essentials
142
3
143
Black lesions • The differential diagnosis of a single black macule
DERMOSCOPY - The Essentials
or papule could be melanocytic or nonmelanocytic,
General principles benign, or malignant.
• Clinically, black color is not always ominous. • What should be done on finding a black lesion?
• Black color with dermoscopy is also not always Check it out with dermoscopy before making
ominous. another move.
144
3
145
DERMOSCOPY - The Essentials
146
3
*
*
148
3
149
DERMOSCOPY - The Essentials
150
3
* *
151
Blue lesions • It is imperative to develop a complete differential
DERMOSCOPY - The Essentials
diagnosis for blue lesions.
General principles • If you see a lesion with blue color but it also has
• Blue color can be seen in benign and malignant other criteria, it should be evaluated like any other
lesions. They are not all blue nevi. lesion.
• Blue color indicates that melanin is deep in the • Blue lesions can be tricky. If in doubt, do not
dermis. hesitate—cut it out.
152
3
153
DERMOSCOPY - The Essentials
154
3
155
Reticular lesions • Reticular pattern ¼ significant areas with pigment
DERMOSCOPY - The Essentials
network.
General principles • Is the pigment network typical or atypical?
• Take a bird’s-eye (global) view of the entire lesion • What other criteria are there to make the
to get a first impression. dermoscopic diagnosis?
156
3
157
DERMOSCOPY - The Essentials
*
*
158
3
159
Spitzoid lesions • Asymmetrical Spitzoid pattern ¼ rule out
DERMOSCOPY - The Essentials
melanoma.
General principles • The stereotypical starburst pattern is seen more
• Spitzoid means similar in appearance to a starburst frequently than the globular pattern, which is more
pattern. common than the nonspecific Spitzoid pattern.
• Spitzoid differential diagnosis includes Clark
(dysplastic) nevus, Spitz nevus, and melanoma. Caution
• Spitzoid morphology comprises a light-dark or blue Deaths have occurred secondary to metastatic “Spitz”
central area and dots and globules or streaks at the nevi that were in reality melanomas. Excise the vast
periphery. majority of Spitzoid lesions. It is better to be safe than
• Symmetrical Spitzoid pattern ¼ benign lesion. sorry.
160
3
162
3
163
Special nevi • Special nevi can be clinically easily diagnosed, and
DERMOSCOPY - The Essentials
in most cases, dermoscopy simply confirms the
General principles clinical diagnosis.
• Special nevi are defined as benign melanocytic nevi • A special history of injury or incomplete surgical
that exhibit a rather specific constellation of removal provides further clues for the diagnosis of
features resulting often in a targetoid or iris-like traumatized and recurrent nevi.
appearance. • Special rules have been established for the
• The group of nevi with special features includes management of special nevi.
Sutton nevi, Meyerson nevi, traumatized nevi,
recurrent nevi, combined nevi, and cockade nevi.
164
3
165
DERMOSCOPY - The Essentials
166
3
167
Multiple Clark (dysplastic) nevi • The “ugly duckling” pigmented skin lesion seen
DERMOSCOPY - The Essentials
both clinically and with dermoscopy warrants a
General principles histopathologic diagnosis.
• Examining multiple nevi with dermoscopy is cost- • If a patient has multiple high-risk-looking lesions
effective and provides information about whether a with dermoscopy, excise one or two to make a
patient has multiple high-risk or banal nevi. dermoscopic-pathologic correlation.
• Most patients with multiple nevi have low-risk • The true number of melanomas is small compared
lesions, but this can be confirmed by checking to the number of patients with multiple dysplastic
them out with dermoscopy. nevi. The vast majority do not need to be excised
• Ask patients whether they have any new or but can be followed using digital systems to look
changing nevi. Never ignore the patient’s history. for significant changes over time.
168
3
169
DERMOSCOPY - The Essentials
*
* *
170
3
171
Follow-up of melanocytic lesions • There are several follow-up protocols including
DERMOSCOPY - The Essentials
short-term follow-up after 3 months, intermediate-
General principles term follow-up after 6-12 months, and long-term
• A high number of nevi, particularly when clinically monitoring over years.
atypical, is the strongest risk factor for the • However, for patient compliance, the first follow-
development of de novo melanoma. Early evolving up visit after baseline documentation should be
melanomas are often not recognizable, as they are scheduled after 3 months, and then, depending on
small, uniformly colored and regularly outlined, the situation, every 6-12 months.
and consequently, mistaken for an otherwise • With the exception of nevi in childhood or young
common nevus. Because most melanomas arise adolescence, any lesion in adults showing even
de novo, the main challenge in the management of subtle changes after 3 months’ follow-up, or with
patients with multiple, atypical nevi represents the asymmetric enlargement accompanied by
identification of initial melanomas hiding among a significant structural changes after 6-12 months,
sea of nevi. should be excised.
• Total-body photography and periodic digital • Equivocal nodular or blue lesions must never be
dermoscopic monitoring improve the early followed up but should be immediately excised
recognition of melanoma, as it adds information at the time of visit. This is because, in the case
about the evolution over time, which in turn of melanoma, the tumor will be already invasive and
assists in diagnosis. The premise behind digital even a 3 months’ delay may worsen the prognosis.
follow-up is that stable lesions are biologically • Growing nevi in childhood or young adolescence are
indolent and thus of no concern, whereas some of characterized by a peripheral rim of globules or by
the new and/or changing lesions may prove to be peripheral streaks in the case of flat evolving
melanomas. These initial melanomas, if followed pigmented Spitz/Reed nevi. When performing digital
over months to years, will eventually manifest follow-up, it should be kept in mind that these nevi
enough atypical clinical criteria allowing for their tend to enlarge symmetrically, the growth being at
discovery. times accompanied by structural changes.
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Lesions with regression white veil. These can now be diagnosed as blue-
DERMOSCOPY - The Essentials
white structures.
General principles • Blue-white structures are high-risk criteria seen in
• A bone-white color often represents scarring seen in melanomas or Spitz nevi.
regression. • Superficial spreading melanomas often have areas
• Do not confuse hypopigmentation with regression. of regression.
• A blue-white veil is a bluish groundglass-appearing • If even a hint of a blue-white structure is identified,
area that can also be seen with regression. it is better to err on the side of caution and make a
• At times it is not possible to tell whether one is histopathologic diagnosis.
dealing with a white area of regression or a blue-
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Flat lesions on the face • Do not expect to see “classic” site-specific criteria. If
DERMOSCOPY - The Essentials
there is a possible site-specific criterion, then
General principles consider it to be one.
• The clinical appearance and initial “gut” • Many high-risk lesions on the head and neck area
impressions should not be ignored when are relatively featureless. Look for subtle high-risk
evaluating flat brown lesions on the head and neck. clues such as different shades of color
• Do not confuse the follicular ostia of a melanocytic asymmetrically located in the lesion.
lesion with the milia-like cysts of a seborrheic
keratosis. Many times you will not be able to tell
the difference.
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Nodular lesions on the face • A macular component to a nodular lesion should raise
DERMOSCOPY - The Essentials
the index of suspicion that the lesion could be high risk.
General principles • A soft compressible nodule that can be easily moved
• The differential diagnosis of pigmented and from side to side favors low-risk pathology. Do not
nonpigmented nodules on the face includes hesitate to palpate or squash lesions down and move
melanocytic, nonmelanocytic, benign, and them from side with the instrumentation used.
malignant lesions. Quite often, the clinical • The main differential diagnosis for nodular lesions
appearance is nonspecific, and dermoscopy will on the face are nevi and basal cell carcinomas.
help in making a clinical diagnosis. Nodular melanoma is rarely found in this area. Do
• Nodules often have ridges and fissures. Do not not forget squamous cell carcinomas including
confuse pigmentation in the fissures with an keratoacanthomas.
atypical pigment network.
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Pigmented lesions of the nails pigmented bands, irregular blotches, irregular dots
DERMOSCOPY - The Essentials
and globules, and Hutchinson’s sign.
General principles • Blood can be found in NAM, so look for high-risk
• Dermoscopy makes the nail apparatus clearer. criteria if you find blood in the nail.
• Nail-apparatus melanoma (NAM) accounts for • The chance of finding high-risk pathology in the
1-2% of melanomas in the lighter skinned pediatric population is low; therefore, a worrisome
population and 15-20% of melanomas in darker history might be more important than a high-risk
skinned people. dermoscopic appearance.
• Amelanotic NAM exists, so pink color—beware.
• High-risk dermoscopic criteria suggestive of NAM
include asymmetry of color and structure, irregular
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Mucosal lesions • Brown-black color—melanocytic.
DERMOSCOPY - The Essentials
• If a pigmented skin lesion looks worrisome
General principles clinically, shows asymmetry of color and structure,
• Most pigmented lesions on mucosal surfaces are and has melanoma-specific criteria, it does not
low risk. matter where on the body it is located. These
• Determine whether the lesion is black, brown, blue, criteria are high risk and warrant a histopathologic
or red. diagnosis.
• Red-blue color—nonmelanocytic.
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Differential diagnostic value of blood Melanocytic lesions
DERMOSCOPY - The Essentials
vessels • Dermal nevi—comma-shaped vessels.
General principles • Clark (dysplastic) nevi—comma-shaped and dotted
vessels.
• Blood vessels can be seen in melanocytic, • Melanoma—dots and irregular linear vessels or
nonmelanocytic, benign, and malignant lesions. milky-red areas.
• Vessels can be seen with other criteria, or vessels
may be the only criterion found in a lesion. Nonmelanocytic lesions
• Some vessels are associated with high-risk
• Basal cell carcinoma—thick branching (arborizing)
pathology and others with low-risk pathology.
vessels.
• Pink lesions with vessels may be melanocytic,
• Seborrheic keratosis—hairpin vessels.
nonmelanocytic, benign, or malignant. The shape
• Bowen’s disease—small foci of dotted vessels that
of the vessels may provide a clue to the correct
look like glomeruli in the kidney.
diagnosis.
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Amelanotic and partially pigmented • Dotted and linear irregular vessels are suggestive of
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Dermoscopy tests Blanching test
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Further reading
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Bories N, Dalle S, Debarbieux S, et al: Dermoscopy of Ferrara G, Argenyi Z, Argenziano G, et al:
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fully regressive cutaneous melanoma. Br J Dermatol The influence of clinical information in the
158:1224–1229, 2008. histopathologic diagnosis of melanocytic skin
Bowling J, Argenziano G, Azenha A, et al: Dermoscopy neoplasms. PLoS ONE 4, e5375. 2009.
key points: recommendations from the Ferrara G, Argenziano G, Soyer HP, et al: The spectrum
international dermoscopy society. Dermatology of Spitz nevi: a clinicopathologic study of 83 cases.
214:3–5, 2007. Arch Dermatol 141:1381–1387, 2005.
Braun RP, Gaide O, Oliviero M, et al: The significance Ferrara G, Argenziano G, Soyer HP, et al: Dermoscopic
of multiple blue-grey dots (granularity) for the and histopathologic diagnosis of equivocal
dermoscopic diagnosis of melanoma. Br J Dermatol melanocytic skin lesions: an interdisciplinary study
157:907–913, 2007. on 107 cases. Cancer 95:1094–1100, 2002.
Braun RP, Rabinovitz H, Kopf AW, et al: Dermoscopic Ferrara G, Giorgio CM, Zalaudek I, et al: Sclerosing
diagnosis of seborrheic keratosis. Clin Dermatol Nevus with pseudomelanomatous features (nevus
20:270–272, 2002. with regression-like fibrosis): clinical and
Braun RP, Rabinovitz H, Tzu JE, et al: Dermoscopy dermoscopic features of a recently characterized
research—an update. Semin Cutan Med Surg histopathologic entity. Dermatology 219:202–208,
28:165–171, 2009. 2009.
Braun RP, Rabinovitz HS, Kopf AW, et al: Pattern Ferrara G, Soyer HP, Malvehy J, et al: The many faces
Analysis. A two-step procedure for the dermoscopic of blue nevus: a clinicopathologic study.
diagnosis of melanoma. Clin Dermatol 20:236–239, J Cutan Pathol 34:543–551, 2007.
2002. Ferrari A, Buccini P, Covello R, et al: The ringlike
Carli P, de Giorgi V, Chiarugi A, et al: Addition of pattern in vulvar melanosis: a new dermoscopic
dermoscopy to conventional naked-eye clue for diagnosis. Arch Dermatol 144:1030–1034,
examination in melanoma screening: a randomized 2008.
study. J Am Acad Dermatol 50:683–689, 2004. Friedman RJ, Rigel DS, Silverman MK, et al: Malignant
Carli P, De Giorgi V, Crocetti E, et al: Improvement of melanoma in the 1990’s: the continued importance
malignant/benign ratio in excised melanocytic of early detection and the role of physician
lesions in the ‘dermoscopy era’: a retrospective study examination and self-examination of the skin.
1997–2001. Br J Dermatol 150:687–692, 2004. CA Cancer J Clin 41:201–226, 1991.
Carli P, De Giorgi V, Giannotti B: Dermoscopy and Giacomel J, Zalaudek I: Dermoscopy of superficial
early diagnosis of melanoma: the light and the basal cell carcinoma. Dermatol Surg 31:1710–1713,
dark. Arch Dermatol 137:1641–1644, 2001. 2005.
Carli P, De Giorgi V, Naldi L, et al: Reliability and Grin CM, Friedman KP, Grant-Kels JM: Dermoscopy:
inter-observer agreement of dermoscopic diagnosis a review. Dermatol Clin 20:641–646, 2002.
of melanoma and melanocytic naevi. Dermoscopy Grob JJ, Bonerandi JJ: The ‘ugly duckling’ sign:
Panel. Eur J Cancer Prev 7:397–402, 1998. identification of the common characteristics of nevi
Carli P, Massi D, DeGiorgi V, et al: Clinically and in an individual as a basis for melanoma screening.
dermoscopically featureless melanoma: when Arch Dermatol 134:103–104, 1998.
prevention fails. J Am Acad Dermatol 46:957–959, Haenssle HA, Korpas B, Hansen-Hagge C, et al:
2002. selection of patients for long-term surveillance with
de Giorgi V, Massi D, Salvini C, et al: Thin melanoma digital dermoscopy by assessment of melanoma
of the vulva: a clinical, dermoscopic-pathologic risk factors. Arch Dermatol 146:257–264, 2010.
case study. Arch Dermatol 141:1046–1047, 2005. Haenssle HA, Korpas B, Hansen-Hagge C, et al: Seven-
Debarbieux S, Ronger-Salve S, Dalle S, et al: point checklist for dermatoscopy: performance
Dermoscopy of desmoplastic melanoma: report of during 10 years of prospective surveillance of
six cases. Br J Dermatol 159:360–363, 2008. patients at increased melanoma risk. J Am Acad
Dolianitis C, Kelly J, Wolfe R, et al: Comparative Dermatol 62:785–793, 2010.
performance of 4 dermoscopic algorithms by Haenssle HA, Krueger U, Vente C, et al: Results from
nonexperts for the diagnosis of melanocytic lesions. an observational trial: digital epiluminescence
Arch Dermatol 141:1008–1014, 2005. microscopy follow-up of atypical nevi increases the
Dupuy A, Dehen L, Bourrat E, et al: Accuracy of sensitivity and the chance of success of
standard dermoscopy for diagnosing scabies. conventional dermoscopy in detecting melanoma.
J Am Acad Dermatol 56:53–62, 2007. J Invest Dermatol 126:980–985, 2006.
Felder S, Rabinovitz H, Oliviero M, et al: Dermoscopic Hofmann-Wellenhof R, Blum A, Wolf IH, et al:
differentiation of a superficial basal cell carcinoma Dermoscopic classification of atypical melanocytic
and squamous cell carcinoma in situ. Dermatol Surg nevi (Clark nevi). Arch Dermatol 137:1575–1580,
32:423–425, 2006. 2001.
218
Inui S, Nakajima T, Nakagawa K, et al: Clinical sensitivity and classification errors. Melanoma Res
Further reading
significance of dermoscopy in alopecia areata: 11:495–501, 2001.
analysis of 300 cases. Int J Dermatol 47:688–693, Malvehy J, Puig S, Argenziano G, et al: Dermoscopy
2008. report: proposal for standardization. Results of a
Iyatomi H, Oka H, Celebi M, et al: Computer-based consensus meeting of the International
classification of dermoscopy images of melanocytic Dermoscopy Society. J Am Acad Dermatol 57:
lesions on acral volar skin. J Invest Dermatol 84–95, 2007.
128:2049–2054, 2008. Malvehy J, Puig S: Dermoscopic patterns of benign
Johr RH: Pink lesions. Clin Dermatol 20:189–296, 2002. volar melanocytic lesions in patients with atypical
Kenet RO, Kang S, Kenet BJ, et al: Clinical diagnosis of mole syndrome. Arch Dermatol 140:538–544,
pigmented lesions using digital epiluminescence 2004.
microscopy. Grading protocol and atlas. Arch Marghoob AA, Braun R: Proposal for a revised 2-step
Dermatol 129:157–174, 1993. algorithm for the classification of lesions of the
Kenet RO, Kenet BJ: Risk stratification. A practical skin using dermoscopy. Arch Dermatol
approach to using epiluminescence microscopy/ 146:426–428, 2010.
dermoscopy in melanoma screening. Dermatol Clin Marghoob AA, Scope A: The complexity of diagnosing
19:327–335, 2001. melanoma. J Invest Dermatol 129:11–13, 2009.
Kittler H, Binder M: Follow-up of melanocytic skin Marghoob AA, Terushkin V, Dusza SW, et al:
lesions with digital dermoscopy: risks and benefits. Dermatologists, general practitioners, and the best
Arch Dermatol 138:1379, 2002. method to biopsy suspect melanocytic neoplasms.
Kittler H, Guitera P, Riedl E, et al: Identification of Arch Dermatol 146:325–328, 2010.
clinically featureless incipient melanoma using Massone C, Hofmann-Wellenhof R, Ahlgrimm-Siess V,
sequential dermoscopy imaging. Arch Dermatol et al: Melanoma screening with cellular phones.
142:1113–1119, 2006. PLoS ONE 2, e483. 2007.
Kittler H, Pehamberger H, Wolff K, et al: Diagnostic Mayer J: Systematic review of the diagnostic accuracy
accuracy of dermoscopy. Lancet Oncol 3:159–165, of dermatoscopy in detecting malignant
2002. melanoma. Med J Aust 167:206–210, 1997.
Kittler H, Pehamberger H, Wolff K, et al: Follow-up Menzies SW, Crotty KA, Ingvar C, et al: An atlas of
of melanocytic skin lesions with digital surface microscopy of pigmented skin lesions:
epiluminescence microscopy: patterns of dermoscopy, 2003, McGraw-Hill.
modifications observed in early melanoma, atypical Menzies SW, Emery J, Staples M, Davies S, McAvoy B,
nevi, and common nevi. J Am Acad Dermatol Fletcher J, et al: Impact of dermoscopy and short-
43:467–476, 2000. term sequential digital dermoscopy imaging for the
Kittler H, Seltenheim M, Dawid M, et al: Frequency and management of pigmented lesions in primary care:
characteristics of enlarging common melanocytic a sequential intervention trial. Br J Dermatol
nevi. Arch Dermatol 136:316–320, 2000. 161:1270–1277, 2009.
Kittler H: Early recognition at last. Arch Dermatol Menzies SW, Gutenev A, Avramidis M, et al: Short-
144:533–534, 2008. term digital surface microscopic monitoring of
Kolm I, Di Stefani A, Hofmann-Wellenhof R, et al: atypical or changing melanocytic lesions.
Dermoscopy patterns of halo nevi. Arch Dermatol Arch Dermatol 137:1583–1589, 2001.
142:1627–1632, 2006. Menzies SW, Ingvar C, Crotty KA, et al: Frequency and
Kreusch JF: Vascular patterns in skin tumors. morphologic characteristics of invasive melanomas
Clin Dermatol 20:248–254, 2002. lacking specific surface microscopic features.
Lin J, Koga H, Takata M, et al: Dermoscopy of Arch Dermatol 132:1178–1182, 1996.
pigmented lesions on mucocutaneous junction and Menzies SW, Ingvar C, McCarthy WH: A sensitivity
mucous membrane. Br J Dermatol 161:1255–1261, and specificity analysis of the surface microscopy
2009. features of invasive melanoma. Melanoma Res
Lipoff JB, Scope A, Dusza SW, et al: Complex 6:55–62, 1996.
dermoscopic pattern: a potential risk marker for Menzies SW, Kreusch J, Byth K, et al: Dermoscopic
melanoma. Br J Dermatol 158:821–824, 2008. evaluation of amelanotic and hypomelanotic
Lorentzen HF, Weismann K, Secher L, et al: The melanoma. Arch Dermatol 144:1120–1127, 2008.
dermatoscopic ABCD rule does not improve Menzies SW, Westerhoff K, Rabinovitz H, et al: Surface
diagnostic accuracy of malignant melanoma. microscopy of pigmented basal cell carcinoma.
Acta Derm Venereol 80:223, 2000. Arch Dermatol 136(8):1012–1016, 2000.
Lorentzen HF, Weismann K, Larsen FG: Structural Menzies SW: A method for the diagnosis of primary
asymmetry as a dermatoscopic indicator of cutaneous melanoma using surface microscopy.
malignant melanoma: a latent class analysis of Dermatol Clin 19:299–305, 2001.
219
Niederkorn A, Ahlgrimm-Siess V, Fink-Puches R, et al: Ronger S, Touzet S, Ligeron C, et al: Dermoscopic
DERMOSCOPY - The Essentials
Frequency, clinical and dermoscopic features of examination of nail pigmentation. Arch Dermatol
benign papillomatous melanocytic naevi (Unna 138:1327–1333, 2002.
type). Br J Dermatol 161:510–514, 2009. Rosado B, Menzies S, Harbauer A, et al: Accuracy of
Noor O, Nanda A, Rao BK: A dermoscopy survey to computer diagnosis of melanoma: a quantitative
assess who is using it and why it is or is not being meta-analysis. Arch Dermatol 139:361–367, 2003.
used. Int J Dermatol 48:951–952, 2009. Rubegni P, Sbano P, Burroni M, et al: Melanocytic skin
Oliveria SA, Geller AC, Dusza SW, et al: The lesions and pregnancy: digital dermoscopy analysis.
Framingham school nevus study: a pilot study. Skin Res Technol 13:143–147, 2007.
Arch Dermatol 140:545–551, 2004. Saida T, Koga H: Dermoscopic patterns of acral
Pagnanelli G, Soyer HP, Argenziano G, et al: melanocytic nevi: their variations, changes, and
Diagnosis of pigmented skin lesions by significance. Arch Dermatol 143:1423–1426, 2007.
dermoscopy: web-based training improves Saida T, Oguchi S, Ishihara Y: In vivo observation of
diagnostic performance of non-experts. magnified features of pigmented lesions on volar
Br J Dermatol 148:698–702, 2003. skin using video macroscope. Usefulness of
Pan Y, Gareau DS, Scope A, et al: Polarized and epiluminescence techniques in clinical diagnosis.
nonpolarized dermoscopy: the explanation for the Arch Dermatol 131:298–304, 1995.
observed differences. Arch Dermatol 144:828–829, Saida T, Oguchi S, Miyazaki A: Dermoscopy for acral
2008. pigmented skin lesions. Clin Dermatol 20:279–285,
Pehamberger H, Binder M, Steiner A, et al: In vivo 2002.
epiluminescence microscopy: improvement of early Salopek TG, Kopf AW, Stetanoto CM, et al:
diagnosis of melanoma. J Invest Dermatol 100 Differentiation of atypical moles (dysplastic nevi)
(Suppl.):356–625, 1993. from early melanoma by dermoscopy. Dermatol
Pehamberger H, Steiner A, Wolff K: In vivo Clin 19:337–345, 2001.
epiluminescence microscopy of pigmented skin Schiffner R, Schiffner-Rohe J, Vogt T, et al:
lesions. I. Pattern analysis of pigmented skin Improvement of early recognition of lentigo
lesions. J Am Acad Dermatol 17:571–583, 1987. maligna using dermatoscopy. J Am Acad Dermatol
Pellacani G, Cesinaro AM, Longo C, et al: 42:25–32, 2000.
Microscopic in vivo description of cellular Seidenari S, Pellacani G, Martella A, et al: Instrument-,
architecture of dermoscopic pigment network in age- and site-dependent variations of dermoscopic
nevi and melanomas. Arch Dermatol 141:147–154, patterns of congenital melanocytic naevi: a
2005. multicentre study. Br J Dermatol 155:56–61, 2006.
Peris K, Ferrari A, Argenziano G, et al: Dermoscopic Seidenari S, Pellacani G: Surface Microscopy features of
classification of Spitz/Reed nevi. Clin Dermatol congenital nevi. Clin Dermatol 20:263–267, 2002.
20:259–262, 2002. Silipo V, De Simone P, Mariani G, et al: Malignant
Pizzichetta MA, Talamini R, Piccolo D, et al: The melanoma and pregnancy. Melanoma Res
ABCD rule of dermatoscopy does not apply to 16:497–500, 2006.
small melanocytic skin lesions. Arch Dermatol Skvara H, Teban L, Fiebiger M, et al: Limitations of
137:1376–1378, 2001. dermoscopy in the recognition of melanoma.
Pizzichetta MA, Talamini R, Stanganelli I, et al: Arch Dermatol 141:155–160, 2005.
Amelanotic/hypomelanotic melanoma: clinical Soyer HP, Argenziano G, Chimenti S, et al:
and dermoscopic features. Br J Dermatol Dermoscopy of pigmented skin lesions. Eur J
150:1117–1124, 2004. Dermatol 11:270–277, 2001.
Puig S, Argenziano G, Zalaudek I, et al: Melanomas Soyer HP, Argenziano G, Ruocco V, et al: Dermoscopy
that failed dermoscopic detection: a combined of pigmented skin lesions (Part II). Eur J Dermatol
clinicodermoscopic approach for not missing 11:483–498, 2001.
melanoma. Dermatol Surg 33:1262–1273, 2007. Soyer HP, Argenziano G, Talamini R, et al: Is
Rabinovitz H, Kopfa AW, Katz B: Dermoscopy: dermoscopy useful for the diagnosis of melanoma?
a practical guide. CD ROM version, 1999, MMA Arch Dermatol 137:1361–1363, 2001.
Worldwide Group Inc. Soyer HP, Argenziano G, Zalaudek I, et al: Three-point
Rajpara SM, Botello AP, Townend J, et al: Systematic checklist of dermoscopy. A new screening method
review of dermoscopy and digital dermoscopy/ for early detection of melanoma. Dermatology
artificial intelligence for the diagnosis of 208:27–31, 2004.
melanoma. Br J Dermatol 161:591–604, 2009. Soyer HP, Hofmann-Wellenhof R, Massone C, et al:
Robinson JK, Nickoloff BJ: Digital epiluminescence Ozdemir F, et al telederm.org: freely available
microscopy monitoring of high-risk patients. online consultations in dermatology. PLoS Med 2,
Arch Dermatol 140:49–56, 2004. e87. 2005.
220
Soyer HP, Kenet RO, Wolf IH, et al: care physicians using skin surface microscopy.
Further reading
Clinicopathological correlation of pigmented skin Br J Dermatol 143:1016–1020, 2000.
lesions using dermoscopy. Eur J Dermatol 10:22–28, Wolf I: Dermoscopic diagnosis of vascular lesions.
2000. Clin Dermatol 20:273–275, 2002.
Soyer HP, Massone C, Ferrara G, et al: Limitations of Wolff K: Why is epiluminescence microscopy
histopathologic analysis in the recognition of important? Recent Results Cancer Res 160:125–132,
melanoma: a plea for a combined diagnostic 2002.
approach of histopathologic and dermoscopic www.dermoscopy.org Consensus Net Meeting on
evaluation. Arch Dermatol 141:209–211, 2005. Dermoscopy (CNMD) 2000. Unifying concepts of
Soyer HP, Smolle J, Hodl S, et al: Surface microscopy. Dermoscopy.
A new approach to the diagnosis of cutaneous Yadav S, Vossaert KA, Kopf AW, et al: Histopathologic
pigmented tumors. Am J Dermatopathol 11:1–10, correlates of structures seen on dermoscopy
1989. (epiluminescence microscopy). Am J Dermatopathol
Soyer HP, Smolle J, Leitinger G, et al: Diagnostic 15:297–305, 1993.
reliability of dermoscopic criteria for detecting Zaballos P, Blazquez S, Puig S, et al: Dermoscopic
malignant melanoma. Dermatology 190:25–30, pattern of intermediate stage in seborrhoeic
1995. keratosis regressing to lichenoid keratosis: report of
Steiner A, Binder M, Schemper M, et al: Statistical 24 cases. Br J Dermatol 157:266–272, 2007.
evaluation of epiluminescence microscopic criteria Zaballos P, Daufı́ C, Puig S, et al: Dermoscopy of
for melanocytic pigmented skin lesions. J Am Acad solitary angiokeratomas: a morphological study.
Dermatol 29:581, 1993. Arch Dermatol 143:318–325, 2007.
Steiner A, Pehamberger H, Binder M, et al: Pigmented Zaballos P, Llambrich A, Cuéllar F, et al: Dermoscopic
Spitz nevi: improvement of the diagnostic accuracy findings in pyogenic granuloma. Br J Dermatol
by epiluminescence microscopy. J Am Acad 154:1108–1111, 2006.
Dermatol 27:697–701, 1992. Zaballos P, Puig S, Llambrich A, et al: Dermoscopy of
Steiner A, Pehamberger H, Wolff K: In vivo dermatofibromas: a prospective morphological
epiluminescence microscopy of pigmented skin study of 412 cases. Arch Dermatol 144:75–83, 2008.
lesions. II. Diagnosis of small pigmented Zalaudek I, Argenziano G, Di Stefani A, et al:
skin lesions and early detection of malignant Dermoscopy in general dermatology. Dermatology
melanoma. J Am Acad Dermatol 17:584–591, 1987. 212:7–18, 2006.
Stolz W, Braun-Falco O, Bilek P, et al: Color atlas of Zalaudek I, Argenziano G, Ferrara G, et al: Clinically
dermatoscopy, ed 2. Oxford, England, 2002, equivocal melanocytic skin lesions with features
Blackwell Scientific Publications. of regression: a dermoscopic-pathological study.
Stolz W, Schiffner R, Burgdorf WH: Dermatoscopy for Br J Dermatol 150:64–71, 2004.
facial pigmented skin lesions. Clin Dermatol Zalaudek I, Argenziano G, Leinweber B, et al:
20:276–278, 2002. Dermoscopy of Bowen’s disease. Br J Dermatol
Tripp JM, Kopf AW, Marghoob AA, et al: Management 150:1112–1116, 2004.
of dysplastic nevi: a survey of fellows of the Zalaudek I, Argenziano G, Mordente I, et al: Nevus
American Academy of Dermatology. J Am Acad type in dermoscopy is related to skin type in white
Dermatol 46:674–682, 2002. persons. Arch Dermatol 143:351–356, 2007.
van der Rhee JI, Bergman W, Kukutsch N: The impact of Zalaudek I, Argenziano G, Soyer HP, et al: Three-point
dermoscopy on the management of pigmented lesions checklist of dermoscopy: an open internet study.
in everyday clinical practice of general dermatologists: Br J Dermatol 154:431–437, 2006.
a prospective study. Br J Dermatol 2009. Zalaudek I, Docimo G, Argenziano G: Using
Vestergaard ME, Macaskill P, Holt PE, et al: dermoscopic criteria and patient-related factors for
Dermoscopy compared with naked eye the management of pigmented melanocytic nevi.
examination for the diagnosis of primary Arch Dermatol 145:816–826, 2009.
melanoma: a meta-analysis of studies performed in Zalaudek I, Giacomel J, Argenziano G, et al:
a clinical setting. Br J Dermatol 159:669–676, 2008. Dermoscopy of facial nonpigmented actinic
Warshaw EM, Lederle FA, Grill JP, et al: Accuracy of keratosis. Br J Dermatol 155:951–956, 2006.
teledermatology for nonpigmented neoplasms. Zalaudek I, Giacomel J, Cabo H, et al:
J Am Acad Dermatol 60:579–588, 2009. Entodermoscopy: a new tool for diagnosing skin
Warshaw EM, Lederle FA, Grill JP, et al: Accuracy of infections and infestations. Dermatology 216:14–23,
teledermatology for pigmented neoplasms. J Am 2008.
Acad Dermatol 61:753–765, 2009. Zalaudek I, Hofmann-Wellenhof R, Soyer HP, et al:
Westerhoff K, McCarthy WH, Menzies SW: Increase in Naevogenesis: new thoughts based on dermoscopy.
the sensitivity for melanoma diagnosis by primary Br J Dermatol 154:793–794, 2006.
221
Zalaudek I, Kittler H, Marghoob AA, et al: Time required vascular structures seen with dermoscopy Part II.
DERMOSCOPY - The Essentials
for a complete skin examination with and without Nonmelanocytic skin tumors. J Am Acad Dermatol
dermoscopy: a prospective, randomized multicenter 63:377–386, 2010.
study. Arch Dermatol 144:509–513, 2008. Zalaudek I, Manzo M, Savarese I, et al:
Zalaudek I, Kreusch J, Giacomel J, et al: How to The morphologic universe of melanocytic nevi.
diagnose nonpigmented skin tumors: a review of Semin Cutan Med Surg 28:149–156, 2009.
vascular structures seen with dermoscopy Part I. Zampino MR, Corazza M, Costantino D, et al: Are
Melanocytic skin tumors. J Am Acad Dermatol melanocytic nevi influenced by pregnancy?
63:361–374, 2010. A dermoscopic evaluation. Dermatol Surg
Zalaudek I, Kreusch J, Giacomel J, et al: How to 32:1497–1504, 2006.
diagnose nonpigmented skin tumors: a review of
222
ERRNVPHGLFRVRUJ
Index
Note: Page numbers followed by b Age of patient, taking account of Asymmetry (color or structure)
indicate boxes, f indicate figures and (Continued) (Continued)
t indicate tables. nail-apparatus pigmentation, 195f seborrheic keratosis, 6f, 24f, 99f,
Spitz nevus on leg of middle-aged 120f, 123f, 124f, 126f, 182f
A woman, 72f solar lentigo, 80f
Acanthotic epidermis, 78 Algorithms (analysis criteria), 1–2, 33 Spitz nevus see Spitz nevus
Acral lesions Amelanotic melanoma see under spitzoid lesion, 90f
asymmetry of color/structure, 105f, Melanoma Atypical pigment network
189f Anamnestic data, melanoma diagnosis, Clark (dysplastic) nevus see Clark
benign type, 102f, 104f 64f (dysplastic) nevus
blue-white structures, 189f Angiokeratoma melanoma see Melanoma
dermoscopic principles, 100–106, multicomponent global pattern, nevus (nevi) see under Nevus (nevi)
188–191 78 Spitz nevus, 13f
dots and globules, 102f, 103f, red-blue lacunas, 107
189f Annular-granular structures B
fibrillar pattern, 104f, 105f actinic keratosis, pigmented, 99f Back, nevi on, 143f
follow-up, 105f definition, 93 Basal cell carcinoma
lattice-like pattern, 101f, 103f lentigo maligna, 95f arborizing vessels, 10f, 53f, 56f, 107,
management approach, 103f lentigo maligna melanoma, 95f 108f, 109f, 110f, 111f, 112f,
melanoma and, 101f, 106f, lichen planus-like keratosis, 183f 113f, 116f, 186f
189f melanoma see Melanoma absent, 117f
multiple colors, 103f seborrheic keratosis, 182f atypical, 109f
nevus, 101f, 189f Antibiotic treatment, Meyerson nevus, microarborizing, 110f, 116f
parallel-furrow pattern, 101f, 102f 165f present outside lesion, 113f
parallel patterns, types, 100–106, Arborizing vessels, 107 asymmetry, 10f, 11f, 15f, 19f, 31f,
100b basal cell carcinoma see under Basal 32f, 186f
parallel-ridge pattern, 106f, 189f cell carcinoma blood vessel appearance, 53f, 94f,
furrow pattern vs, 102f dermal nevus, 56f, 186f 112f, 153f, 204f
plantar surfaces, pressure areas, microarborizing, in basal cell small linear, 115f
105f carcinoma, 110f, 116f blue-gray blotches, 107, 108f, 109f,
in situ melanoma, differential Asymmetrically pigmented follicles, 110f, 111f, 112f, 113f, 114f,
diagnosis, 106f, 190f 94f, 96f 115f, 116f, 117f
‘string of pearls,’ 101f, 103f, 106f, description, 93 absent, 117f
189f, 190f seborrheic keratosis, 182f blue-white structures, 10f, 11f, 15f,
subcorneal hemorrhage, 191f Asymmetry (color or structure) 19f, 31f, 32f, 108f, 115f, 154f
Acrosyringia, 101f, 103f acral melanocytic lesions, 105f crusts surrounding mini-ulcerations,
Actinic keratosis, 97f, 99f actinic keratosis, 97f 113f
Actinic lentigo, seborrheic keratosis basal cell carcinoma see under Basal differential diagnosis
evolving from, 99f cell carcinoma amelanotic melanoma vs, 185f,
Adolescents Clark (dysplastic) nevus, 12f, 21f 204f
evolving nevi, 173f combined nevus, 77f blue nevus vs, 109f, 112f
follow-up of lesions, 172 congenital nevus, 63f dermal nevus vs, 56f
globular nevus seen in, 43f inkspot lentigo, 150f dermatofibroma vs, 110f
melanoma in, 142f keratoacanthoma, 187f hemangioma vs, 110f
Sutton nevus, 165f labial lentigines, 198f keratoacanthoma vs, 187f
see also Pediatric patients lentigo maligna, 183f melanoma vs, 11f, 78, 88f, 94f,
Age of patient, taking account of, 12f melanoma see Melanoma 108f, 110f, 112f, 114f, 116f,
melanoma nevus (nevi), 4f, 6f, 8f, 17f, 20f, 26f, 117f, 153f, 154f, 202f, 204f
on 45-year old women, multiple 27f, 28f, 29f, 31f nevus vs, 25f, 53f
nevi, 175f slight asymmetry, 12f, 14f, 21f, seborrheic keratosis vs, 110f, 124f,
before or following puberty, 140f 25f, 26f, 41f 127f
223
Basal cell carcinoma (Continued) Blood vessels (Continued) Blue nevus (Continued)
DERMOSCOPY - The Essentials
globules, 153f dermal nevus, 201f history, 155f
gray zone, 115f dermatofibroma, 137f homogeneous color, 27f, 67f, 155f
hairs never seen in, 185f, 186f diagnostic value of homogeneous pattern, 33, 64f, 67f
irregular dots and globules, 154f general dermoscopic principles, 200 hypomelanotic melanoma vs, 66f
leaf-like area, 114f, 117f melanocytic lesions, 200 milia-like cysts, 155f
multicomponent global pattern, 78 non-melanocytic lesions, 200–206 nodular melanoma vs, 153f
nodular, 10f, 31f, 32f, 113f dotted, 201f, 202f, 203f, 205f, 206f, pigment network, absent, 27f
differential diagnosis, 25f, 117f, 207, 209f, 214f stereotypical, 64f, 65f
187f hairpin-shaped, 202f, 204f, 205f symmetry of color and structure, 27f
on face, 185f, 186f, 187f keratoacanthoma, 187f, 204f whitish area in, 65f, 66f
pigment network linear irregular, 202f, 203f, 205f, 207 Blue-white structures
absent, 10f, 11f, 15f, 19f, 31f, 32f melanoma, 116f, 187f, 202f, 203f basal cell carcinoma see under Basal
heavy pigmentation, 116f, 117f amelanotic and partially cell carcinoma
pink color, 110f, 115f, 116f, 117f pigmented, 207–210, 208f, blue nevus, 66f
pressing down hard a danger for, 108f 209f, 210f bluish dots and globules confused
stereotypical, 111f renal glomerulus type appearance, with (nevi), 54f
ulceration, 110f, 111f, 112f, 113f, Bowen’s disease, 206f and central hypopigmentation, 29f
115f, 132f, 153f, 154f seborrheic keratosis, 205f Clark (dysplastic) nevus, 35f, 51f,
Biopsy Spitz nevus, 69f, 141f, 202f 178f
Clark (dysplastic) nevus, 48f thrombosed, hemangioma, 129f, congenital nevus, 58f
clear cell acanthoma, 206f 132f as high-risk, 176
labial lentigines, 198f partially thrombosed, 131f, 133f melanoma see Melanoma
labial lentigo, 197f vascular patterns, polymorphic, 205f as melanoma-specific criterion, 1
metastatic melanoma, 155f Blotches multiple anastomosing, 22f
nodular lesions, 109f acral melanocytic lesions, 104f nevus see Nevus (nevi)
seborrheic keratosis, 123f, 124f, black see Black blotch seborrheic keratosis, 24f, 121f, 123f
126f, 205f blue-gray see Blue-gray blotches Spitz nevus see Spitz nevus
solar lentigo, 181f irregular Bony white areas
Spitz nevus, 75f brownish, nevus, 53f, 59f melanoma, 78
Black blotch, melanoma, 87f Clark nevus see under Clark regression associated, 36f, 38f, 41f,
Black color/lesions (dysplastic) nevus 176
differential diagnosis, 144 inkspot lentigo, 150f Borderline lesion, characteristics, 23f
general dermoscopic principles, melanoma see under Melanoma Bowen’s disease, 200
144–147 recurrent nevi, 166f Brown pseudonetwork
lamella see Black lamella Spitz nevus, 163f actinic keratosis, 97f
melanoma, 151f regular, 78 seborrheic keratosis, 125f
nonspecific, 145f subungual hemorrhage, 193f
recurrent nevi, 166f Blue-gray blotches, 107 C
seborrheic keratosis, 124f basal cell carcinoma, 108f, 109f, Central hyperpigmentation see under
Spitz nevus, 70f, 72f, 75f 110f, 111f, 112f, 113f, 114f, Hyperpigmentation
Black dots/globules 115f, 116f, 117f Central hypopigmentation see under
melanoma, 88f absent, 117f Hypopigmentation
nevus (nevi), 6f seborrheic keratosis, 127f Central white patch
Black lamella, 36f Blue lesions dermatofibroma, 107, 135f,
Black nevus see under Nevus (nevi) basal cell carcinoma, 153f, 154f 137f
Blanching test, 211 general dermoscopic principles, melanoma vs, 209f
Clark (dysplastic) nevus, 214f 152–155 description, 107–137
dermal nevus, 215f melanoma, 154f Changes in lesions
Blood nodular, on face, 153f melanoma, 175f
nail-apparatus melanoma, 192 melanoma metastasis, 155f reticular pattern, 33
subcorneal hemorrhage, 191f nevi see Blue nevus see also Follow-up of lesions
Blood vessels Blue nevus Children see Pediatric patients
arborizing see Arborizing vessels asymmetry, 67f Chrysalis-like structures, melanoma, 5f,
basal cell carcinoma, 53f, 94f, 112f, atypical, 112f 88f
204f blue-white structures, 27f, 66f Clark (dysplastic) nevus
small linear vessels, 115f congenital, combined with, 167f adjacent to benign dermal, 39f
Bowen’s disease, 206f differential diagnosis, 64f, 65f, 66f, asymmetry, 12f, 21f
Clark (dysplastic) nevus, 201f 67f, 109f, 112f, 155f atypical pigment network, 42f, 51f,
clear cell acanthoma, 206f diffuse bluish-brown pigmentation, 151f, 157f, 158f, 170f
comma-like vessels, nevus, 53f, 55f, 67f severe atypia, 83f, 84f
201f fibrosis, 65f slight, 38f
Clark (dysplastic) nevus, 201f firm nodule with smooth surface, 66f blanching test, 211, 214f
224
Clark (dysplastic) nevus (Continued) Color, asymmetry of see Asymmetry Dermatofibroma (Continued)
Index
blotches, 170f (color or structure) milia-like cysts, 136f
blue-white structures, 35f, 51f, 78, Combined nevus pigment network, 135f, 136f, 137f
178f asymmetry, 77f pink color, 137f
benign type, 179f definition, 167f reticular depigmentation, 136f
central hyperpigmentation, 40f, 42f melanoma vs, 39f, 77f, 167f, 210f seborrheic keratosis vs, 136f
central hypopigmentation, 158f targetoid appearance, 167f stereotypical, 135f, 137f
comma-shaped vessels, 201f Comedo-like openings Dermoscopy
compound type, 38f description, 107 algorithms (analysis criteria), 1–2,
globular pattern, 48f follicular ostia vs, 95f 33
reticular-globular pattern, 39f nevus, 54f, 55f, 56f, 60f definition, 1
differential diagnosis dermal, 201f goals, 1
blue nevus vs, 65f seborrheic keratosis, 107, 118f, 119f, technique, 1
melanoma vs, 39f, 69f, 83f, 87f, 120f, 121f, 122f, 123f, 124f, 3-point checklist, 1–32
88f, 91f 125f, 126f, 147f, 205f Dermoscopy tests see Tests,
in situ melanoma vs, 21f, 38f, 42f, Comma-shaped vessels dermoscopy
61f, 157f nevus, 53f, 55f, 201f Digital dermoscopic monitoring
Spitz nevus vs, 12f, 50f, 69f, 71f, 73f Clark (dysplastic) nevus, 201f evolving nevi, 173f
superficial melanoma vs, 84f Congenital melanocytic nevus melanoma recognition, 172
diffuse homogeneous pigmentation, asymmetry, 63f, 140f Spitz nevus, 174f
50f biopsy indicated where, 139 Dots and globules
dots and globules, 35f, 48f, 157f, blue, combined with, 167f acral melanocytic lesions, 102f, 103f,
170f, 201f blue-white structures, 58f 189f
dotted vessels, 201f facial, 62f blue-gray globules, melanocytic
eccentric hyperpigmentation, 38f follow-up, 63f, 140f lesions, 116f
featureless, 170f globular-homogenous pattern, 60f Bowen’s disease, 206f
fibrosis, 178f globular pattern, 33, 58f, 59f, 63f irregular
finger-like projection, broken-up cobblestone-like shape, 140f inkspot lentigo, 150f
pigment network intermingled hairs, 61f as melanoma-specific criterion, 78
with globules, 39f multicomponent global pattern, 78 nevus, globular pattern, 48f
globular pattern, 33, 58f pediatric patients, 140f recurrent nevi, 166f
hypopigmentation, homogeneous, pigment network, 58f Spitz nevus, 75f, 76f
38f reticular-homogenous pattern, 63f see also Melanoma
junctional type, 40f reticular pattern, 58f lichen planus-like keratosis, 183f
line segmentation, 35f in situ melanoma arising in, 140f nevus (nevi) see under Nevus (nevi)
multifocal hypopigmentation, 58f, stereotypical, 58f reddish dots, 124f, 127f
170f starburst pattern, 33
multiple, 168–171 D Dysplastic nevus see Clark (dysplastic)
peppering, 179f Deep shave biopsy nevus
pigment network Clark (dysplastic) nevus, 48f
atypical, see above seborrheic keratosis, 126f E
broken-up, 39f De novo melanoma, 172 Eccrine duct openings, in Spitz nevus,
fading out, 35f, 157f Depigmentation, Sutton nevus, 165f 71f
irregular, 61f Dermal nevus Eczematous nevus, 165f
subtle remnants, 201f arborizing vessels, 56f Erythema, Clark (dysplastic) nevus,
and regression, 65f, 177f, 178f, 179f basal cell carcinoma vs, 56f 214f
reticular-globular pattern, 39f blanching test, 215f Evolving nevus (nevi), 173f
reticular-homogenous pattern, 38f blood vessels, 201f Excisional shave biopsy, seborrheic
reticular pattern, 35f, 40f, 151f, 157f, blue nevus vs, 66f keratosis, 123f, 126f
158f on face, 185f, 186f Exophytic papillary structures/ridges
variation, 42f papillomatous, 55f, 56f, 215f nevus (nevi), 56f, 60f
with severe atypia, 83f comedo-like openings, 54f, 55f, intermingled with furrows, 57f
‘ugly duckling’ lesion, 171f 56f, 60f, 107
verrucous melanoma arising within, skin-colored nodule, vs melanoma, F
90f 89f Face
Clear cell acanthoma, 206f see also Blue nevus; Clark (dysplastic) congenital melanocytic nevus on,
Clinical scenarios, common, 139–215 nevus; Nevus (nevi); Spitz nevus 62f
Cobblestone pattern Dermatofibroma diagnosis difficulties, 99f
cockade nevi, 167f basal cell carcinoma vs, 110f flat lesions on, 181f, 182f, 183f
congenital melanocytic nevus, 140f blue nevus vs, 66f general dermoscopic principles,
melanoma, 140f central white patch, 107, 135f, 136f, 180–183
nevus (nevi), 46f, 140f 137f lentigo maligna on, 181f
Cockade nevi, 167f melanoma vs, 209f melanoma-specific criteria, 93–99
225
Face (Continued) Globular-starburst pattern, Spitz nevus, Hemosiderotic targetoid nevi, 166f
DERMOSCOPY - The Essentials
nodular lesions on, 184–187 73f History of patient, taking account of,
basal cell carcinoma, 184, 185f, Globules see Dots and globules 12f, 67f, 186f
186f Gray color, seborrheic keratosis, 124f Homogeneous pattern
dermal nevus, 185f, 186f Gray pseudonetwork description, 33
differential diagnosis, 184 description, 93–99 nevus see Nevus (nevi)
general dermoscopic principles, lentigo maligna, 94f, 95f reticular-homogenous pattern
184–187 lentigo maligna melanoma, 95f see Reticular-homogenous
keratoacanthoma, 187f Gray zone lesions pattern
nodular melanoma on, 153f basal cell carcinoma, 115f Homogeneous-starburst pattern, Spitz
pseudopigment network, 122f common nature of, 139 nevus, 72f, 73f
seborrheic keratosis, 99f, 126f melanoma, 81f Honeycomb pattern see Reticular
solar lentigo on, 181f nevus (nevi), 51f pattern
Spitz tumor, atypical, 142f Hutchinson’s sign, nail-apparatus
see also under Lentigo maligna; H melanoma, 195f
Lentigo maligna melanoma Hair follicles Hypergranulosis, blue-white structures,
‘Fat fingers,’ seborrheic keratosis, 99f, holes representing, nevus, 57f, 59f 78
125f solar lentigo, 98f Hyperkeratosis, in keratinizing tumors,
Fibrillar pattern see under Acral white-appearing, actinic keratosis, 204f
melanocytic lesions 97f Hypermelanotic nevus, tape
Fibroangioma, 130f, 134f Hair/hairs test, 211
Fibrosis and basal cell carcinoma, 185f, 186f Hyperpigmentation
blue nevus, 65f congenital melanocytic nevus, 61f, blotches as, 78
blue-white structures, 78 140f see also Blotches
Clark (dysplastic) nevus, 178f Hairpin vessels central, Clark (dysplastic) nevus, 40f,
fibroangioma, 130f keratoacanthoma, 204f 42f
hemangioma, 129f, 132f, 133f, 134f melanoma, 202f eccentric
Kaposi’s sarcoma, 134f seborrheic keratosis, 205f Clark (dysplastic) nevus, 38f
melanoma, 178f Halo nevi, 165f nevus, reticular pattern, 38f
Fluid, dermoscopy technique, 1 Hand, Spitz nevus on, 147f paracentral, nevus, 41f
Follicular openings, seborrheic Head and neck lesions, ostia of perifollicular, 140f
keratosis, 85f, 126f, 139 appendages, 8f Hypopigmentation
Follicular ostia Hemangioma blue-white structures vs, 78
facial melanocytic lesions, 93–99 basal cell carcinoma vs, 110f central
seborrheic keratosis vs, 139 blue-white color, 129f, 133f Clark (dysplastic) nevus, 158f
Follow-up of lesions bluish color, 64f, 131f nevus, 29f, 41f
acral melanocytic, 105f cherry (senile), 129f, 132f homogeneous, 36f, 38f, 40f
in child/adolescent, 172 dark-red to blue-black lacunas, 130f, melanoma, 91f, 171f, 210f
labial lentigines, 198f 132f multifocal
labial lentigo, 197f differential diagnosis Clark (dysplastic) nevus, 58f,
nevus (nevi), 40f, 42f, 47f, 49f, 51f, 52f fibroangioma vs, 134f 170f
congenital nevus, 63f, 140f melanoma vs, 132f melanoma, 171f
evolving, 173f fenestrated whitish pattern, 130f, nevus, 21f
Spitz nevus, 174f 132f nevus see under Nevus (nevi)
in situ melanoma, 175f fibrosis, 129f, 132f, 133f, 134f perifollicular, 140f
Freckles, surrounding inkspot lentigo, lobular capillary, 130f vs regression, 176
148 melanoma vs, 131f seborrheic keratosis, 121f
nevus vs, 64f Hypopigmentation islands, nevus, 34f,
G purplish lacunas, 128f, 133f 58f
Genital nevus, 199f pyogenic granuloma vs, 133f
Giant congenital melanocytic nevus, red-blue lacunas, 107, 129f, 131f, I
pediatric patients, 139 133f, 134f Inflammation, Meyerson nevus, 165f
Globular-homogenous pattern reddish-black areas, 131f Injury, of pre-existing nevus, 166f
nevus (nevi), 57f red lacunas, 128f Inkspot lentigo
nevus spilus, 60f thrombosed vessels, 129f, 132f asymmetry of color/structure, 150f
Spitz nevus, 75f, 77f partially thrombosed, 131f, 133f general dermoscopic principles,
Globular pattern white color, 128f 148–151
Clark (dysplastic) nevus see Clark Hemorrhage irregular blotches, 150f
(dysplastic) nevus in middle of nail plate, 194f irregular dots and globules, 150f
cockade nevi, 167f reddish blotches of blood, 194f melanoma vs, 151f
description, 33 streaks representing, 187f pigment network, 149f, 150f
nevus see Nevus (nevi) subcorneal, 191f, 213f stereotypical, 149f
Spitz nevus see Spitz nevus subungual, 193f variation, 149f, 150f
226
In situ melanoma Lentigo maligna (Continued) Melanoma (Continued)
Index
acral, differential diagnosis, 106f, 190f on nose, 181f Clark (dysplastic) nevus vs, 88f
atypical pigment network, 38f, 157f rhomboid structures, 94f, 95f, 119f, featureless melanoma, 6f
congenital nevus, arising in, 140f 183f gray pseudonetwork, 93–99, 95f
differential diagnosis seborrheic keratosis vs, 124f, 139 lentigo maligna, 95f
black nevus vs, 52f Lentigo maligna melanoma, 95f lentigo maligna melanoma, 95f
Clark (dysplastic) nevus vs, 21f, Lichen planus-like keratosis, 183f multiple colors, 79f, 91f
38f, 42f, 61f, 157f Line segmentation, pigment network with regression, 177f, 178f
full melanoma, 21f melanoma, 5f slight, 96f
lentigo maligna vs, 94f nevus, 3f, 29f, 34f, 36f, 49f atypical pigment network, 1, 2t, 3f,
nevus vs, 30f, 36f Clark (dysplastic), 35f, 157f, 158f 5f, 7f, 9f, 15f, 16f, 18f, 19f, 21f,
Spitz nevus vs, 70f, 73f congenital, 58f 23f, 78, 79f, 81f, 85f, 86f, 89f,
early, diagnosis difficulty, 159f reticular pattern, 33, 34f 151f, 159f, 162f, 175f
follow-up, 175f Lip, labial lentigo, 197f absent, 16f
irregular dots and globules see under Lobular capillary hemangioma, 130f Clark nevus vs, 83f, 88f
Dots and globules debatable, 10f, 11f
irregular streaks, 157f M description, 78
within pre-existing nevus, 38f Macrophages, melanoma, 208f in five positive criteria, 78
reticular pattern, 157f Melanocytes, 78, 95f irregular dots/globules with, 80f
with eccentric hyperpigmentation, Melanocytic lesions blood vessels, 116f, 187f, 202f,
38f acral see Acral melanocytic lesions 203f
Instrumentation list, dermoscopy, 1 congenital nevus see Congenital blue-white color, 79f
Irregular blotches melanocytic nevus blue-white structures, 1, 2t, 3f, 4f, 5f,
nevus (nevi), 53f, 59f dermal nevus, 200 7f, 8f, 9f, 10f, 11f, 13f, 15f, 16f,
see also Melanoma follow-up, 172–175 18f, 21f, 23f, 30f, 79f, 80f, 81f,
Irregular streaks see Streaks, irregular globules, 121f 82f, 83f, 84f, 85f, 86f, 87f, 91f,
Irritation blue-gray, 116f 92f, 146f, 154f, 158f, 161f, 162f,
hemosiderotic targetoid nevi, 166f nevi see Clark (dysplastic) nevus; 163f
melanoma, 84f Nevus (nevi); Spitz nevus extensive, 91f
nevus (nevi), 56f reticular pattern, 40f, 127f five positive criteria, 78–92
seborrheic keratosis, 84f, 126f, 205f see also Melanoma irregular blotches with, 91f
Melanoma irregular dots and globules with,
J acral lesions and, 101f, 106f, 189f 85f, 88f, 91f
Jelly sign, solar lentigo, 97f, 181f in adolescents, 142f multiple anastomosing, 22f
amelanotic with peppering, 19f
K basal cell carcinoma vs, 108f, 114f, spitzoid melanoma, 90f
Kaposi’s sarcoma 116f, 117f, 204f streaks with, 5f, 89f
fibroangioma vs, 130f blood vessels, 207–210, 208f, vivid color, 85f
hemangioma vs, 134f 209f, 210f vulva, melanoma of, 199f
red lacunas, 134f dermatofibroma vs, 137f bony white areas, 36f, 38f, 41f, 78
Keratoacanthoma, 187f featureless, 203f color and structure
blood vessels, 204f fibroangioma vs, 130f asymmetry of see above
general dermoscopic principles, dark color, 22f
L 207–210 comma-shaped vessels not seen in,
Labial lentigines, 198f nail-apparatus melanoma, 192 55f
Labial lentigo, 197f partially pigmented, 207–210 de novo, 172
Lacunas pyogenic granuloma vs, 133f dermoscopy accuracy, 1, 2
borders, 129f seborrheic keratosis vs, 205f desmoplastic, 137f
see also under Hemangioma skin-colored nodule, 89f diagnosis by 3-checklist, 1–32
Lattice-like pattern see under Acral Spitz nevus vs, 77f, 202f diagnosis by five melanoma-specific
melanocytic lesions vascular patterns, 205f local criteria see Melanoma-
Lentigo annular-granular structures, 96f specific criteria below
inkspot see Inkspot lentigo gray granules, 95f differential diagnosis
solar see Solar lentigo appearance of new structures, 175f acral melanocytic lesion vs,
unstable, 94f arising in nevus, 83f 101f
Lentigo maligna asymmetrically pigmented follicles, basal cell carcinoma vs, 11f, 78,
actinic keratosis vs, 99f 94f, 96f 88f, 94f, 108f, 110f, 112f, 114f,
annular-granular structures, 95f asymmetry of color/structure, 1, 2t, 116f, 117f, 153f, 154f, 202f,
asymmetry of color/structure, 183f 3f, 4f, 5f, 7f, 8f, 9f, 10f, 11f, 13f, 204f
classical pattern of early, 96f 15f, 16f, 18f, 19f, 21f, 22f, 23f, blue nevus vs, 27f, 64f, 66f, 67f,
facial, 94f, 95f, 96f 30f, 79f, 80f, 82f, 83f, 85f, 86f, 155f
gray pseudonetwork, 94f, 181f 90f, 92f, 96f, 179f, 202f, 208f, Clark (dysplastic) nevus vs, 21f,
melanocytes, 95f 210f 69f, 83f, 87f, 88f, 91f
227
Melanoma (Continued) Melanoma (Continued) Melanoma (Continued)
DERMOSCOPY - The Essentials
combined nevus vs, 39f, 77f, 167f, irregular streaks, 5f, 78, 79f, 80f, 81f, streaks, 151f, 159f, 161f
210f 82f, 83f, 86f, 88f, 89f, 92f, 154f, irregular see above
hemangioma vs, 130f, 131f, 132f 159f, 162f, 163f square, 142f
inkspot lentigo vs, 151f absent, 91f subungual, 193f
nevus spilus vs, 60f basal cell carcinoma vs, 114f superficial see Superficial melanoma
nevus vs, 38f, 60f, 61f, 64f, within blotch, 81f traumatized, 166f
169f in five positive criteria, 78 ‘ugly duckling’ lesion, 171f, 209f
seborrheic keratosis vs, 6f, 84f, irregular vessels, 202f, 203f ulceration, 132f
85f, 91f, 127f, 202f, 203f irritated, 84f verrucous, 90f
Spitz nevus vs, 12f, 69f, 70f, 71f, lentigo maligna see Lentigo maligna vulval, 199f
72f, 74f, 75f, 76f, 77f, 202f line segmentation, broken-up, 5f white color, 208f, 209f
distinguishing criteria, 1, 3f, 7f melanoma-specific criteria, 79f, 80f, yellowish globules, 8f
dots and globules 81f, 82f, 83f, 84f, 85f, 86f, 87f, Melanophages
cobblestone-like shape, 140f 88f, 89f, 90f, 91f, 92f, 142f, blue-white structures, 78
irregular see below 151f, 158f dots and globules, 78
small red dots, 209f identification of, 146f black and bluish pepper-like,
dotted vessels, 203f site-specific, 94f, 95f, 96f, 97f, 98f, 85f
early, 18f, 76f, 169f 99f infiltrate, 35f
eccentric area, 91f metastatic inkspot lentigo, 149f
EGF (Elevated Firm Growing) rule, blue nevus vs, 27f, 64f, 155f lichen planus-like keratosis, 183f
207 mimicking hemangioma, 130f nevus (nevi), 35f
enlargement, 175f milia-like cysts, 107 regressing melanoma, 61f, 209f,
featureless, 6f, 83f, 91f, 107 milky-red background, 203f 210f
fibrosis, 178f multicomponent global pattern, 78, Meyerson nevus, 165f
follicular ostia, 95f 79f, 82f, 83f, 85f, 86f Microarborizing vessels, basal cell
gray pseudonetwork, 93–99, 95f in nevus spilus, 62f carcinoma, 110f, 116f
gray zone, 81f nodular Milia-like cysts
hairpin vessels, 202f basal cell carcinoma vs, 109f, 112f, blue nevus, 155f
hypomelanotic 117f, 153f dermatofibroma, 136f
arising within superficial blue nevus vs, 27f, 64f, 155f description, 107
melanoma or pre-existing Clark on face, 153f follicula ostia vs, 95f
nevus, 39f hypomelanotic, arising within a melanoma, 91f, 182f
basal cell carcinoma vs, 113f superficial melanoma/pre- nevus, 43f, 53f, 60f
blue nevus vs, 66f existing Clark nevus, 39f dermal, 201f
hypopigmentation, 91f, 171f, 210f skin-colored, 89f seborrheic keratosis, 6f, 8f, 43f, 53f,
information, keeping from patients, Spitz nevus vs, 67f, 76f 91f, 94f, 107, 118f, 119f, 120f,
159f thin and ulcerated, 84f 121f, 122f, 123f, 124f, 139, 182f
invasive, 154f parallel-ridge pattern, acral Milky-red background
irregular blotches, 81f, 82f, 84f, 85f, melanoma, 106f melanoma, 203f
89f, 91f, 146f patchy reticular pattern, 87f Spitz nevus, 141f, 202f
blue-gray, 140f pigment network, 91f warning, 141f, 203f
brownish, 87f absence of, 9f, 13f, 30f, 84f, Moth-like appearance, solar lentigo,
in five positive criteria, 78 91f 80f, 97f, 98f, 181f
grayish, 208f, 210f atypical, see above Mucosal lesions
horeshoe-shaped, 163f pink color, 82f, 96f, 163f, 179f, 208f, general dermoscopic principles,
irregular streaks within, 81f 209f, 210f 196–199
melanoma-specific criteria, 158f reddish color, 84f, 171f genital nevus, 199f
spitzoid lesion, 90f reflection artifact, 81f labial lentigines, 198f
irregular dots and globules, 78, 79f, regression, 177f, 178f, 179f labial lentigo, 197f, 198f
80f, 81f, 82f, 83f, 84f, 86f, 88f, blue nevus vs, 65f melanoma of vulva, 199f
89f, 91f, 92f, 96f, 142f, 151f, bony white areas, 36f, 38f, 41f venous lake, 197f
154f, 159f, 161f, 175f multifocal hypopigmentation Multiple Clark (dysplastic nevi),
acral lesions, 190f verging on, 171f 168–171
black, 85f, 88f nevus vs, 36f, 61f
bluish ‘pepper-like’ dots, 85f in superficial melanoma, 86f, 92f, N
brownish, 87f 176 Nail-apparatus melanoma (NAM), 192
in five positive criteria, 78 rhomboid structures, 93, 96f Hutchinson’s sign, 195f
melanoma-specific criteria, 158f in situ see In situ melanoma masquerading as blood, 194f
reddish dots, 208f as spitzoid lesion, 90f, 92f, 161f, Nails, pigmented lesions
seborrheic keratosis vs, 85f 162f, 163f general dermoscopic principles,
spitzoid lesion, 90f starburst pattern, 161f 192–195
vulva, melanoma of, 199f statistical analysis, 1 hemorrhage, 193f, 194f
228
Nails, pigmented lesions (Continued) Nevus (nevi) (Continued) Nevus (nevi) (Continued)
Index
nail-apparatus melanoma, 192, Clark (dysplastic) nevus, 35f, 48f, hypopigmentation, 38f
195f 157f, 170f central, 29f
masquerading as blood, 194f closely packed, 43f, 46f homogeneous, 36f
nevus (nevi), 195f cobblestone-like shape, 46f, 140f multifocal, 21f, 58f
Nevus (nevi) and comedo-like openings, 54f hypopigmentation islands, 34f, 58f
acral see Acral melanocytic lesions dark-brown, 35f, 46f, 57f hypopigmented areas, 37f, 59f
asymmetry of color/structure, 4f, 6f, dermal nevi, 186f intradermal, 107
8f, 17f, 20f, 26f, 27f, 28f, 29f, exophytic papillary structures/ irregular blotches, 53f, 59f
31f, 48f, 63f ridges resembling globules, 56f irritated, 56f
slight, 12f, 14f, 21f, 25f, 26f, 41f flat brownish area with, 55f junctional
atypical see Clark (dysplastic) nevus globular pattern, 43f Clark (dysplastic) nevus, 40f
atypical pigment network, 14f, 20f, irregular, brownish, 48f compound, difficult to
26f, 27f, 28f, 29f, 30f, 51f numerous, 43f, 58f differentiate, 34f, 35f, 43f
absent, 4f, 17f, 22f, 23f, 28f regular, 146f parakeratosis, 211
see also Pigment network below reticular pattern, 35f line segmentation, pigment network
black, 28f rim of brown pigmentation see under Line segmentation,
reticular-homogenous pattern, 52f surrounding, 46f pigment network
tape stripping, 52f slightly irregular, 51f melanoma arising within, 83f
tape test, 211 subtle, 44f melanoma features, none seen, 32f
blue see Blue nevus tiny dots, central part, 50f Meyerson, 165f
blue-white structures, 12f, 23f, 31f uneven distribution, 44f, 48f milia-like cysts, 43f, 53f, 60f
absent, 4f, 6f, 7f, 8f, 12f, 14f, 17f, see also Globular pattern below movement from side to side, 55f
22f, 26f, 28f, 29f, 30f dysplastic see Clark (dysplastic) multifocal hypopigmentation, 21f,
bluish dots and globules confused nevus 58f
with, 54f enlargement, 173f multiple nevi, 168–171, 169f
diffuse, 35f evolving, 173f follow-up, 175f
present, 20f, 24f, 25f, 28f, 50f, 51f, exophytic papillary structures/ridges, nail-apparatus pigmentation, 195f
57f, 60f, 146f 56f, 60f papillomatous dermal, 55f, 56f
slight, 18f intermingled with furrows, 57f comedo-like openings, 55f, 60f
subtle, 55f featureless, 56f papillomatous surface, 46f, 54f
borderline lesion, 23f flat melanocytic, 34f, 55f, 58f paracentral hyperpigmentation, 41f
central hypopigmentation, 29f, 41f follow-up, 40f, 42f, 47f, 49f, 51f, 52f pediatric patients see under Pediatric
Clark (dysplastic) see Clark congenital nevus, 63f patients
(dysplastic) nevus genital, 199f pigmentation, dark brown, 47f
cockade, 167f globular-homogenous pattern, 57f, pigment network, 21f
color variation, 46f 60f absent, 6f, 12f, 14f, 18f, 20f, 25f
combined see Combined nevus globular pattern, 44f, 46f, 47f, 53f, central-periphery distinctions,
comedo-like openings, 54f, 55f, 56f, 54f, 55f, 56f, 57f, 59f, 61f, 63f 49f
60f basal cell carcinoma vs, 53f fading out at periphery, 34f, 36f,
comma-like vessels, 53f, 55f Clark (dysplastic) nevus, 48f 37f, 41f, 42f, 52f, 127f
common, in men, 42f dark brown pigmentation, 47f patchy, 63f
compound, 46f description, 33 regular, 3f, 7f
junctional, difficult to melanoma arising within nevus, small rim surrounding
differentiate, 34f, 35f, 43f 83f homogeneous
congenital see Congenital overlap of features, 49f hypopigmentation, 36f
melanocytic nevus with reticular pattern, 57f typical, 8f, 12f, 24f, 29f, 34f, 35f,
crypts and furrows, irregular, 56f stereotypical, 43f, 46f 36f, 37f, 41f, 52f, 146f
dark color, 7f, 12f, 23f variations, 43f, 45f, 51f uneven distribution, 37f
dermal see Dermal nevus see also Dots and globules above see also Atypical pigment network
differential diagnosis globules, 20f, 25f above
basal cell carcinoma vs, 25f, 53f, gray zone lesions, 51f pink color, 40f, 48f
56f hemosiderotic targetoid, 166f pseudopigment network, 62f
hemangioma vs, 64f holes representing hair follicles, 57f recurrent, 166f
melanoma vs, 38f, 60f, 61f, round white, 59f Reed (Spitz) see Spitz nevus
64f, 169f homogeneous pattern, 56f, 64f regular pigment network, 3f, 7f
in situ melanoma vs, 30f, 52f blue nevus, 64f, 65f reticular-globular pattern, 39f, 49f,
dots and globules, 43f, 53f bluish pigmentation, 66f, 67f 50f
black (Spitz nevus), 73f diffuse pigmentation, 50f reticular-homogenous pattern, 36f,
bluish, 54f, 59f genital nevus, 199f 40f, 41f, 51f, 52f, 63f
brownish, 57f, 59f reticular, 41f Clark (dysplastic) nevus, 38f
brownish-blue, 53f, 61f, 69f variation in colors, 64f stereotypical reticular, 37f
brown-to-gray, 47f hyperpigmentation, paracentral, 41f variation, 38f
229
Nevus (nevi) (Continued) Parallel-ridge pattern Pigment network (Continued)
DERMOSCOPY - The Essentials
reticular pattern, 42f, 58f, 61f acral melanocytic lesions see Acral negative, in Spitz nevus, 69f
atypical pigment network and, melanocytic lesions nevus (nevi)
42f, 61f vs fibrillar pattern, 104f nevus spilus, 62f
common, in flat acquired malignant nature of, 102f patchy, 37f
melanocytic nevus, 34f melanoma see Melanoma see also under Nevus (nevi)
globular pattern with, 57f vs parallel-furrow pattern, 102f, pseudopigment network vs, 62f
nevus spilus, 62f 106f reticular pattern, 33
patchy, 37f as removal criterion, 106f see also Reticular pattern
pseudopigment network, 62f subcorneal hemorrhage, 213f Spitz nevus see under Spitz nevus
stereotypical, 52f Pattern analysis, 33–138 uneven distribution, 37f
seborrheic keratosis adjacent Pediatric patients Pink color
to, 90f congenital melanocytic nevus, 140f actinic keratosis, 99f
sessile nodule, 54f follow-up of lesions, 172 basal cell carcinoma, 110f, 115f,
soft compressible nature, 54f, 55f, general dermoscopic principles, 116f, 117f
56f, 60f 139–143 dermatofibroma, 137f
Spitz see Spitz nevus giant congenital melanocytic nevus, keratoacanthoma, 187f
starburst pattern, streaks with, 33 139 melanoma see Melanoma
stereotypical, 12f, 43f melanoma, 142f nevus (nevi), 40f, 48f
streaks, 50f nevus (nevi) dermal, 185f
Sutton, 165f on back, 143f Spitz nevus, 77f, 141f
symmetrical, 3f, 7f, 18f, 25f, 28f, 36f, dysplastic see Clark (dysplastic) seborrheic keratosis, 126f, 127f
41f, 59f, 61f, 62f, 63f, 146f nevus Spitz nevus, 202f
traumatized, 166f globular pattern, 47f warning, 48f, 77f, 110f, 137f, 185f
yellowish-white keratotic material, reticular-homogenous pattern, 36f Polarized dermoscopy, 1
56f Spitz nevus, 74f, 139, 141f, 142f, Pseudonetwork
Nevus spilus, 60f 174f brown, 97f, 99f, 125f, 142f
melanoma in, 62f typical, 47f gray
Non-melanocytic lesions see also Adolescents lentigo maligna, 94f, 181f
basal cell carcinoma see under Basal Pigmentary incontinence, seborrheic melanoma, 93–99
cell carcinoma keratosis, 205f seborrheic keratosis, 119f
Bowen’s disease, 200 Pigmentation Pseudopigment network, seborrheic
dermatofibroma, 135f blue nevus see Blue nevus keratosis, 122f
seborrheic keratosis see Seborrheic dark brown nevus, 47f Pseudostarburst pattern, seborrheic
keratosis nail-apparatus, 195f keratosis, 119f
six diagnostic criteria, 107–137 rim of brown, 46f Punch biopsy, labial lentigines, 198f
see also Fibroangioma; Hemangioma; blue nevus, 64f Purple color
Kaposi’s sarcoma; Pyogenic see also Depigmentation; hemangioma, 128f, 133f
granuloma Hyperpigmentation; hemorrhage, 193f
Hypopigmentation; Pigment Pyogenic granuloma
O network fibroangioma vs, 130f
Orthokeratosis, blue-white structures, Pigmented lesions fibrosing, 134f
78 of nails see Nails, pigmented lesions hemangioma vs, 134f
Ostia of appendages of skin, triage, 1–32 red lacunas, 133f
head and neck lesions, 8f see also under Spitz nevus
melanoma, 94f Pigmented Skin Lesion Clinics, 198f R
Pigment network Recurrent nevi, 166f
P absent Red-blue lacunas
Papillomatous dermal nevi, 55f, 56f basal cell carcinoma, 19f description, 107
comedo-like openings, 54f, 55f, 60f, nevi, 6f, 18f, 20f, 28f hemangioma, 107, 129f, 131f,
107 seborrheic keratosis, 24f 134f
seborrheic keratosis vs, 123f atypical see Atypical pigment Reddish dots and globules, seborrheic
Papillomatous melanocytic nevi, network keratosis, 124f, 127f
seborrheic keratosis vs, 118f Clark (dysplastic) nevus see Clark Reddish-whitish color, fibroangioma,
Papillomatous surface, nevi, 46f, 54f (dysplastic) nevus 130f
Parallel-furrow pattern congenital melanocytic nevus, 58f Red lacunas
acral melanocytic lesions see Acral dermatofibroma, 135f, 136f, 137f fibroangioma, 130f
melanocytic lesions fading out hemangioma, 128f
benign nature of, 102f Clark (dysplastic) nevus, 35f Kaposi’s sarcoma, 134f
vs parallel-ridge pattern, 102f, 106f nevus, 34f, 36f, 37f, 41f, 42f, 52f, pyogenic granuloma, 133f
Parallel pattern, acral melanocytic 127f Reed nevus see Spitz nevus
lesions see under Acral line segmentation see Line Reflectance confocal microscopy, 96f
melanocytic lesions segmentation, pigment network Reflection artifacts, white dots, 81f
230
Regression in lesions Seborrheic keratosis (Continued) Solar lentigo (Continued)
Index
bony white areas, 36f, 38f, 41f brown pseudonetwork, 125f pigmentation, 97f, 98f
Clark (dysplastic) nevus, 65f, 177f, comedo-like openings, 107, 118f, seborrheic keratosis arising from,
178f, 179f 119f, 120f, 121f, 122f, 123f, 125f
general dermoscopic principles, 124f, 125f, 126f, 147f, 205f Special nevi
176–179 absent, 127f cockade, 167f
melanoma see under Melanoma differential diagnosis combined see Combined nevus
scarring and, 204f amelanotic melanoma vs, 205f definition, 164
Reticular depigmentation basal cell carcinoma vs, 110f, 124f, general dermoscopic principles,
dermatofibroma, 136f 127f 164–167
Spitz nevus, 77f, 141f dermatofibroma vs, 136f hemosiderotic targetoid, 166f
Reticular-global pattern, Clark lentigo maligna vs, 124f, 139 Meyerson nevus, 165f
(dysplastic) nevus, 39f melanoma vs, 6f, 84f, 85f, 91f, recurrent, 166f
Reticular-globular pattern 127f, 139, 202f, 203f Sutton nevus, 165f
Clark (dysplastic) nevus, 39f papillomatous dermal nevi vs, 123f Spindle cell nevus Reed (Spitz nevus),
nevus (nevi), 49f, 50f papillomatous melanocytic nevi 70f
Reticular-homogenous pattern, 41f vs, 118f Spitz nevus
Clark (dysplastic) nevus, 38f Spitz nevus vs, 119f asymmetry, 72f, 74f, 75f
nevus (nevi), 36f, 40f, 51f, 52f superficial melanoma vs, 125f atypical, 13f, 142f
patchy, 63f facial, 99f, 126f blood vessels, 69f, 141f, 202f
stereotypical reticular, 37f ‘fat fingers,’, 99f, 125f blotches, 163f
variation, 38f flat lesion, 118f, 119f, 122f, 182f blue-white structures, 13f, 68f, 70f,
Reticular lesions follicular openings, 85f, 126f, 139 73f, 74f, 75f, 78, 147f, 158f,
Clark (dysplastic) nevus, 157f, 158f hairpin vessels, 205f 161f, 162f
see also Clark (dysplastic) nevus hypopigmentation, 121f blotch partially covering, 163f
general dermoscopic principles, irritated, 84f, 126f, 205f in child, 74f
156–159 keratotic, adjacent to benign nevus, combined pattern, 77f
melanoma, 157f, 159f 90f differential diagnosis
see also Melanoma milia-like cysts, 6f, 8f, 43f, 53f, 91f, basal cell carcinoma vs, 112f
Spitz nevus, 158f 94f, 107, 118f, 119f, 120f, 121f, blue nevus vs, 67f
see also Spitz nevus 122f, 123f, 124f, 139, 182f Clark (dysplastic) nevus vs, 12f,
Reticular pattern absent, 127f 50f, 69f, 71f, 73f
acral melanocytic lesions, 103f multicomponent global pattern, 78 dermatofibroma vs, 137f
description, 33 opaque color, 120f melanoma vs, 12f, 69f, 70f, 71f,
melanoma, 87f pigmentary incontinence, 205f 72f, 74f, 75f, 76f, 77f, 147f, 202f
nevus see Clark (dysplastic) nevus; pigment network pigmented spindle cell nevus
Nevus (nevi) absent, 24f Reed, 147f
patchy, 37f, 87f diffuse area, 124f seborrheic keratosis vs, 119f
Reticular-starburst pattern, Spitz nevus, pink color, 126f, 127f in situ melanoma vs, 70f, 73f
76f, 158f reddish dots, 124f, 127f diffuse homogeneous pigmentation,
Rhomboid structures reticular pattern, 127f 50f
description, 93 rhomboid structures, 182f dots and globules, rim of, 161f
lentigo maligna, 94f, 95f, 119f, 183f solar lentigo, arising from, 125f fatalities, 160
lentigo maligna melanoma, 95f stereotypical, 122f, 123f flat nonpigmented, 141f
melanoma, 78 streaks, 147f follow-up, 174f
seborrheic keratosis, 182f stuck-on appearance, 123f globular-homogenous pattern, 77f
Rim of brown pigmentation, blue superficial, 124f brownish dots/globules, 75f
nevus, 64f variations, 123f globular pattern/type, 69f, 71f
verrucous surface, 120f black, 75f
S Shave biopsy dots and globule size variations,
Scrape test, 167f Clark (dysplastic) nevus, 48f 75f
subcorneal hemorrhage, 213f labial lentigo, 197f mimicking melanoma, 74f
Seborrheic keratosis seborrheic keratosis, 123f, 126f, 205f prominent dots and globules, 69f
acanthotic type, 123f, 205f Soft compressible nature, nevus, 54f, uneven distribution, 76f
actinic lentigo, evolving from, 99f 55f, 56f, 60f globular-starburst pattern, 73f
annular-granular structures, 182f Solar lentigo homogeneous areas, 142f
asymmetry, 6f, 99f, 120f, 123f, 124f, asymmetry of color, 80f, 181f homogeneous central zone, 75f
126f, 182f on face, 181f homogeneous-starburst pattern, 72f,
slight, 24f lentigo maligna vs, 94f 73f
blood vessels, 205f melanoma-specific criteria, lack of, irregular dots and globules, 75f, 76f
blue-gray blotches, 127f 98f life cycle, 71f
blue-white structures, 24f, 121f, 123f moth-like appearance, 80f, 97f, 98f, management approach, 139
bluish color, 126f 181f melanoma suspicion, 69f
231
Spitz nevus (Continued) Streaks (Continued) Tattoos, 64f
DERMOSCOPY - The Essentials
milky-red background, 141f, 202f irregular Technique (dermoscopy), 1
non-pigmented, 202f description, 78 Telangiectasias, pyogenic granuloma,
pigmentation, black-bluish, 141f melanoma see under Melanoma 133f
pigmented spindle cell nevus Reed, seborrheic keratosis, 125f Tests, dermoscopy
70f, 71f, 74f, 139, 141f, 147f, regular, 99f blanching, 211
174f seborrheic keratosis, 125f, 147f general dermoscopic principles,
pigment network, 71f, 76f Spitz nevus, 50f, 68f, 69f, 70f, 71f, 211–215
absent, 75f 72f, 73f, 74f, 76f, 78, 141f, 147f, scrape test, 167f
atypical, 13f 158f, 161f, 162f, 174f tape test, 211, 212f
jet black, 72f ‘String of pearls’ white dots, acral wobble sign, 169f
multiple colors, 73f, 74f melanocytic lesions, 101f, 103f, Thigh, Spitz nevus on, 141f
negative, 69f, 77f 106f, 189f, 190f 3-point checklist, 1–32
reticular depigmentation, 77f Structure, asymmetry of see Asymmetry see also Asymmetry (color or
superficial black, 70f, 72f, 76f (color or structure) structure); Atypical pigment
variation, 71f Subcorneal hematoma, red-blue network; Blue-white structures
pink color, 77f, 141f, 202f lacunas, 107 Total-body photography, melanoma
reddish color, 141f, 142f Subcorneal hemorrhage, 191f recognition, 172
Reed see above under pigmented scrape test, 213f Traumatized nevi, 166f
spindle cell nevus Reed Subungual hematoma, red-blue Triage, pigmented skin lesions, 1–32
reticular depigmentation, 77f, 141f lacunas, 107
reticular-starburst pattern, 76f, 158f Subungual hemorrhage, 193f U
starburst pattern, 68f, 70f, 72f, 74f, Subungual melanoma, 193f ‘Ugly duckling’ lesion, 168, 171f, 209f
139, 163f Sun damage Ulceration
basal cell carcinoma contrasted, lentigo maligna and, 94f basal cell carcinoma, 110f, 111f,
112f melanoma findings, 80f 112f, 113f, 115f, 132f, 153f,
dots and globules with, 33 seborrheic keratosis, 122f, 125f 154f
with eccrine duct openings, 71f Superficial melanoma melanoma, 132f
globular pattern compared, 160 asymmetry, 84f, 87f, 92f, 210f Unstable lentigo, concept, 94f
seborrheic keratosis contrasted, atypical pigment network, 92f
119f blue-white structure, 84f
V
streaks with, 33 blue-white structures, 92f Vascular patterns see Blood vessels
variant nevus, 70f, 72f Clark (dysplastic) nevus vs, 84f Venous lake, 197f
stereotypical, 68f comedo-like openings, 120f
Vulva, melanoma of, 199f
streaks, 50f, 68f, 69f, 70f, 71f, 72f, hypomelanotic nodular melanoma
73f, 74f, 76f, 78, 141f, 147f, arising within, 39f
158f, 161f, 162f, 174f irregular blotches, 86f, 87f W
symmetrically located, 163f irregular dots and globules, 84f, 92f White color
symmetrical, 69f, 70f, 75f, 161f, 162f brownish to black, 87f in blue-white structures, 21f, 25f
variant, starburst pattern, 70f irregular streaks, 84f, 86f, 87f, 92f central white patch see Central white
see also Spitzoid lesion milia-like cysts, 120f patch
Spitzoid lesion with regression, 86f, 92f, 176, 177f dermatofibroma, 136f
asymmetry, 90f seborrheic keratosis vs, 120f, 125f hemangioma, 128f
differential diagnosis, 160 see also Melanoma keratoacanthoma, 204f
general dermoscopic principles, 160 Sutton nevus, 165f melanoma see Melanoma
melanoma as see under Melanoma Symmetry of color and structure, nevi, White dots
recognition of symmetry/asymmetry 3f, 7f, 18f, 25f, 28f, 36f, 41f, 59f, acral lesions, 189f
in, 162f 61f, 146f acral melanocytic lesions
Squamous cell carcinoma, 187f blue nevus, 27f lattice-like pattern, 101f, 103f
Starburst pattern congenital, 62f, 63f parallel-furrow pattern, 102f
description, 33–77 Spitz nevus, 69f, 70f, 75f, 161f, 162f actinic keratosis, 97f
melanoma, 161f reflection artifacts, 81f
Spitz nevus see Spitz nevus T Wobble sign, 169f
Steroid treatment, Meyerson nevus, Tape stripping
165f black lamella, 36f Y
Streaks black nevus, 52f Yellow color
chrysalis-like structures, melanoma, Tape test, 211 keratotic material, nevus, 56f
5f, 88f black nevus, 212f melanoma, 8f
hemorrhage, 187f Targetoid composition, melanoma, 96f seborrheic keratosis, 126f
232
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