Posttransfusion hyperhemolysis syndrome in beta thalassemia major: Postulation of various mechanisms
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In a multiply transfused beta thalassemia major patient, posttransfusion hyperhemolysis syndrome was attributed to multiple transfusions, anti-Cw antibodies, macrophage hyperactivity, hypersplenism, and erythropoiesis suppression.
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Abstract
Hyperhemolysis syndrome (HS) should be considered in a multiply transfused thalassemia patient. HS in this patient was attributed to a combination of factors including multiple transfusions, presence of anti-Cw, macrophage hyperactivity, hypersplenism and suppression of erythropoiesis.
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