Autoimmune hemolytic anemia in chronic lymphocytic leukemia View PDF
                    *Amelia  Maria Gaman 
Medicine,  University Of Medicine And Pharmacy Of Craiova, Craiova, Romania
                
*Corresponding Author:                            Amelia  Maria Gaman 
                            Medicine,  University Of Medicine And Pharmacy Of Craiova, Craiova, Romania
 Email:gamanamelia@yahoo.com                 
                
Published on: 2014-03-21
Abstract
Chronic lymphocytic leukemia (CLL) is a malignant proliferation of mature, differentiated B-lymphocytes, frequently associated with autoimmune hemolytic anemia (AIHA). The effect of this complication in the clinical outcome and survival of patients with CLL is controversial. The aim of study was to evaluate the prevalence of AIHA in our patients with CLL and how this complication influences the patient's survival.
Keywords
CLL; AIHA; Survival
Introduction
Chronic lymphocytic leukemia (CLL) is a malignant proliferation of mature, differentiated lymphocytes, mostly of B-cell origin, frequently associated with autoimmune cytopenia (autoimmune hemolytic anemia and immune thrombocytopenia). Autoimmune hemolytic anemia (AIHA), defined as an acquired hemolytic anemia in which the destruction of erythrocytes is mediated by anti-erythrocyte auto antibodies, occurs in 5-38% of patients with CLL.
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