Hyperhemolytic transfusion reaction in sickle cell disease
- 1 March 2001
- journal article
- case report
- Published by Wiley in Transfusion
- Vol. 41 (3) , 323-328
- https://doi.org/10.1046/j.1537-2995.2001.41030323.x
Abstract
BACKGROUND: An atypical form of life‐threatening hemolytic transfusion reaction (HTR) in patients with sickle cell disease (SCD) has been well described in the literature. Continuation of blood trans...Keywords
This publication has 26 references indexed in Scilit:
- Monocyte–macrophage system as targets for immunomodulation by intravenous immunoglobulinBlood Reviews, 2000
- Post‐Transfusion Hyperhaemolysis in a Patient with Sickle Cell Disease: Use of Steroids and Intravenous Immunoglobulin to Prevent Further Red Cell DestructionVox Sanguinis, 1995
- Circulating adhesion molecules in diseaseImmunology Today, 1993
- Transfusion of PNH patientsTransfusion, 1990
- Factors Associated with Positive Direct Antiglobulin Tests in Pretransfusion Patients: A Case‐Control StudyVox Sanguinis, 1985
- Increased adherence of sickled and phosphatidylserine-enriched human erythrocytes to cultured human peripheral blood monocytes.Journal of Clinical Investigation, 1985
- Association between H LA and Red Cell AntigensVox Sanguinis, 1978
- A Haemolytic Transfusion Reaction without Demonstrable Antibodies in VitroVox Sanguinis, 1963
- Haemolytic Transfusion Reaction due to Incompatibility without Demonstrable AntibodiesVox Sanguinis, 1960
- Rapid Destruction of Apparently Compatible Red CellsBMJ, 1959