Post‐transfusion hyperhemolysis syndrome in a patient with beta thalassemia major

Post‐transfusion hyperhemolysis syndrome in a patient with beta thalassemia major

Abstract Hyperhemolysis syndrome (HS) is characterized by the occurrence of severe anemia with post‐transfusion hemoglobin and hematocrit levels being markedly lower than those present prior to transfusion. A high index of suspicion of HS in a multi‐transfused thalassemia patient allows prompt insti...

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Bibliographic Details
Main Authors: Ganesh Kasinathan, Jameela Sathar
Format: Article
Language:English
Published: Wiley 2021-06-01
Series:Clinical Case Reports
Subjects:
anti‐Cw
beta thalassemia major
hyperhemolysis syndrome
immunoglobulin
macrophage hyperactivity
Online Access:https://doi.org/10.1002/ccr3.4226

Internet

https://doi.org/10.1002/ccr3.4226

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