HYPERHEMOLYSIS SYNDROME ATTRIBUTABLE TO ANTI-JKB IN A PATIENT WITH SICKLE CELL DISEASE: A CASE REPORT
Introduction: Hyperhemolysis syndrome is an atypical form of transfusion reaction, it has been described with a frequency of 4% in patients with sickle cell anemia after transfusion of apparently compatible red blood cells. It is a rare and serious condition characterized by a drop in hemoglobin aft...
Main Authors: | XPC Huamani, JPM Franz, CK Weber, EC Weinert, CE Wiggers, T Callai, AA Paz |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2023-10-01
|
Series: | Hematology, Transfusion and Cell Therapy |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2531137923013275 |
Similar Items
-
MENINGO-MIELORRADICULOPATIA ASSOCIADA À LEUCEMIA LINFOCÍTICA CRÔNICA: RELATO DE CASO
by: CK Weber, et al.
Published: (2023-10-01) -
LEUCEMIA DE GRANDES LINFÓCITOS GRANULARES, UM RELATO DE CASO
by: EC Weinert, et al.
Published: (2023-10-01) -
LINFOMA DE BURKITT EM PACIENTE IDOSA: UM RELATO DE CASO
by: T Callai, et al.
Published: (2023-10-01) -
RELATO DE CASO: LEUCEMIA LINFOCÍTICA CRÔNICA COM ACOMETIMENTO DE SISTEMA NERVOSO CENTRAL
by: CE Wiggers, et al.
Published: (2023-10-01) -
A fatal case of immune hyperhemolysis with bone marrow necrosis in a patient with sickle cell disease
by: Matthew S. Karafin, et al.
Published: (2017-03-01)