A Case Report of Hyperhemolytic Syndrome in Sickle Cell Disease, with a Special Focus on Avoiding the Use of Transfusions

In patients with sickle cell disease (SCD), transfusions pose risks like delayed hemolytic transfusion reaction (DHTR) and hyperhemolytic syndrome (HHS). We present the case of a 61-year-old Nigerian male patient with SCD, developing hyperhemolytic syndrome (HHS) post-orthopedic surgery due to alloi...

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Bibliographic Details
Main Authors: Omar Obajed Al-Ali, György Pfliegler, Ferenc Magyari, Fanni Borics, László Imre Pinczés, Árpád Illés, Boglárka Brúgós
Format: Article
Language:English
Published: MDPI AG 2024-03-01
Series:Thalassemia Reports
Subjects:
Online Access:https://www.mdpi.com/2039-4365/14/1/3