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Red blood cells alloimmunization and autoimmunization among transfusion-dependent beta-thalassemia patients in Alexandria province, Egypt.
Transfus Apher Sci
August 2015
Immunology Department, Medical Research Institute, Alexandria University, Alexandria, Egypt.
Background: Beta thalassemia is considered a severe, progressive anemia, which needs regular transfusions for life expectancy. One of the most important complications of regular blood transfusions is autoimmunization and alloimmunization, which increases the need for transfusion. This study was performed to investigate the frequency of auto- and allo-antibodies in beta thalassemia patients in Alexandria, Egypt.
View Article and Find Full Text PDF[Autoimmune hemolytic anemia during treatment with cyclosporin after liver transplantation].
Gastroenterol Clin Biol
March 1988
Service d'hépatogastroentérologie, Hôpital E. Herriot, Lyon.
Hemolytic anemia was observed in a 36 year-old liver transplant patient. The immunosuppressive regimen included cyclosporine A and prednisolone. Hemolysis appeared a few days after amoxicillin treatment.
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