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Published byGrace Henry Modified over 8 years ago
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microangiopathic hemolytic anemia
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TTP
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reticulocytes
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Polychromasia
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Autoimmune hemolytic anemia
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Target Cells Increased surface to volume ratio Actually shaped like a bell (3D) Target cells are always hypochromic Excess membrane cholesterol and phospholipid Decreased osmotic fragility
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Hemoglobin C disease Liver disease Iron deficiency Any hemoglobin abnormality Post splenectomy Target Cells
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Target Cells (Codocytes)
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Target Cells
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10 y/o boy of Italian descent Diagnosis : Beta thalassemia major Homozygous beta 0 thalassemia Comment : beta 0 = beta gene producing no beta chains no beta chains and hence no Hb A. untreated he has about 95% Hb F (remainder being Hb A 2 ) Treatment : Transfusion to maintain hemoglobin level; Chelation therapy to remove excess iron present due to hemolysis and transfusions. Bone marrow transplantation is treatment of choice
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Case 2 Howell Jolly Body Sickle cell Erythroblast
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Sickle cells (Drepanocytes)
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Sickle Cells
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