Identification of low frequency anti-erythrocyte antibodies in chronically transfused patient with beta-thalassemia: a case report
DOI:
https://doi.org/10.5433/1679-0367.2015v36n1Suplp325Keywords:
Beta-thalassemia, Alloimmunization. Uncommon antibodies, Anti-Colton b, Anti-Lutheran 14.Abstract
The rate of erythrocyte alloimmunization in tranfusion-dependent patients can reach 50%, although the frequency of clinically relevant antibodies in transfused patients is not fully known, it is estimated that about 1% of patients are sensitized to each unit of transfused RBCs. The aim of this study is to report the case of an 11-year-old girl with ?-thalassemia major, chronically transfused, which was detected in pre-transfusion protocol, the presence of two rare anti-erythrocyte antibodies: anti-Colton b (anti-Cob) and anti-Lutheran 14 (anti-Lu14). To survey the clinical and laboratory patient history, research records filed in the archives of the university hospital in which the patient is monitored system was performed. The phenotyping erythrocyte in multitransfused patients is essential to decrease the risk of complications due to alloimmunization and estimate the availability of compatible blood. Thus, the report of this case may contribute to increase knowledge about of the real frequency of uncommon anti-erythrocyte antibodies in thalassemic patients.
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