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Color Atlas of Hematology - Practical Microscopic and Clinical ...

Color Atlas of Hematology - Practical Microscopic and Clinical ...

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138 Erythrocyte <strong>and</strong> Thrombocyte AbnormalitiesHypochromic Anemia with HemolysisThalassemiasA special form <strong>of</strong> hypochromic anemia mostly affecting patients <strong>of</strong> Mediterrane<strong>and</strong>escent presents with normal erythrocyte count, decreasedMCH, <strong>and</strong> clinical splenomegaly. The smear displays erythrocytes withcentral hemoglobin isl<strong>and</strong>s (target cells). These cells do not necessarilypredominate in the CBC: the most revealing field views show at most 50%target cells in addition to clear anisocytosis <strong>and</strong> frequent basophilic stippling.Occasional normoblasts give a general indication <strong>of</strong> increased erythropoiesis.Although target cells are also nonspecific, since they can occurin such conditions as severe iron deficiency or obstructive jaundice, thisoverall picture should prompt hemoglobin electrophoresis. The sampleconsists <strong>of</strong> ACD-stabilized blood at 1 :10 dilution. A significant increase inthe HbA 2 fraction confirms a diagnosis <strong>of</strong> thalassemia minor, the heterozygousform <strong>of</strong> the disease. Thalassemia major, the homozygous variant, isfar rarer <strong>and</strong> more serious. In this form <strong>of</strong> the disease, in addition to thetarget cells, the CBC shows a marked increase in red precursor cells. Hbelectrophoresisshows a predominance <strong>of</strong> HbF (the other hemolytic anemiasare usually normochromic, see p. 140).

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