Lec 2 Anemia Classification1

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The passage discusses different classifications and types of anemia. It mentions morphological and etiological classifications of anemia and discusses microcytic, hypochromic anemias and iron deficiency anemia in more detail.

The two main classifications of anemia mentioned are morphological classification based on red blood cell size and degree of hemoglobinization, and etiological classification based on the underlying mechanisms causing anemia.

Microcytic, hypochromic anemias are characterized by a mean corpuscular volume (MCV) of less than 80 with pale, poorly hemoglobinized red cells on peripheral smear. They result from a disorder in cytoplasmic maturation caused by reduced hemoglobin production.

ANEMIA CLASSIFICATION

By
DR. ZAHRAA NAJAH
 There
are several classifications of anemia . Two
commonly used are:
1. Morphological classification :based on:
(1) red cell size(normocytic, microcytic, or macrocytic), and
(2) degree of hemoglobinization, reflected by the color of red
cells (normochromic or hypochromic)

2. Etiological classification: Based on the underlying


mechanisms of production of anemia
Morphological classification
Etiological classification
MICROCYTIC,
HYPOCHROMIC,ANEMIAS
An MCV of less than 80 with pale, poorly hemoglobinized red
cells on peripheral smear characterizes this group of anemias.
All result from a disorder in cytoplasmic maturation caused
by reduced hemoglobin production.
Hemoglobin is produced using iron, protoporphyrin and
globin chains so the main cause are:
Iron deficiency anemia
 Main cause:
1. Inadequate intake of iron as in vegetarian diet ,
malabsorption , gastrectomy
2. Blood loss as in menorrhagia, postmenopausal ,esophageal
varices, peptic ulcer, aspirin ingestion.
Physical examination may reveal glossitis, koilonychia (spoon nails),
gastritis, and angular stomatitis.
Replacement therapy is Ferrous Sulfate 300mg TID on empty
stomach. May give with vitamin C to enhance absorbtion.
 Follow – up in 3-4 weeks hemoglobin should be normalized and the
Ferritin should be normal in 8 weeks.
Thalassemia syndromes
It is a genetic disorder of globin production. There is decreased or absence of
synthesis of either α or β-globin chain of adult hemoglobin, Hb A (α2 β2),so to the
type of globin chain that synthesis in reduced amount can classify to alpha &beta
thalassemia
Β-Thalassemia is a hereditary disorder characterized by diminished synthesis of
structurally normal β-globin chains, associated with unimpaired synthesis of α-
chains
Types of Beta thalassemia
Diagnosis of Beta thalassemia
Clinical Laboratory
Anemia of chronic disease
Long-standing infections, neoplastic diseases, and
chronic inflammatory processes (eg, rheumatoid arthritis,
systemic lupus erythematosus) block iron transportation
from the storage sites to the bone marrow factory by
increase hepcidine level.
Sideroblastic anemias
characterized by the presence of “ringed” sideroblasts in the
bone marrow; associated with hypochromic cells on a
peripheral smear.
May be congenital or acquired
Acquired sideroblastic anemias are associated with use of
antituberculous medications (eg, isoniazid, pyrazinamide14),
alcohol abuse, lead poisoning, chronic inflammation .

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