由恒河抗体引起的乘客淋巴细胞综合征引起的肾移植后贫血——一种罕见的常见病因

Dakhin Ad, J. Malheiro, M. Almeida, L. Martins, L. Dias, S. Pedroso, A. Henriques, A. Cabrita
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摘要

移植后贫血(PTA)是一种常见的发现,通常是多因素的。一些非典型的病因可以被通常的原因所掩盖,导致无法解决的贫血和损害移植物活力和宿主恢复。免疫介导的溶血可发生在实体或骨髓移植受体存在abo轻微错配,或更罕见的,其他血型错配,如恒河(Rh)系统。这种情况被称为乘客淋巴细胞综合征(PLS),发生在供体活的b淋巴细胞与移植器官一起移植后,导致产生针对受体红细胞抗原(Ag)的抗体(Ab)。即使PTA病因似乎很明显或没有明显的理由怀疑,也应考虑PLS。我们回顾了一例肾移植后PLS,由Rh(D)不匹配引起。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-Kidney Transplant Anemia as a Result of Passenger Lymphocyte Syndrome by Rhesus Antibodies - A Rare Etiology for a Common Finding
Posttransplant Anemia (PTA) is a common finding, often multifactorial. Some atypical etiologies can be masked by the usual causes, resulting in non-solving anemia and compromising graft viability and host recovery. An immune-mediated hemolysis can develop in solid or bone marrow graft recipients in the presence of ABO-minor mismatch or, more rarely, other blood groups mismatches, like Rhesus (Rh) system. This condition, known by Passenger Lymphocyte Syndrome (PLS), occurs after the transfer of donor’s viable B-lymphocytes with the transplanted organ, which leads to the production of antibodies (Ab) against recipient red blood cells (RBC) antigens (Ag). PLS should be considered even when the PTA etiology seems obvious or when there are no apparent reasons for suspecting it. We review a case of PLS after kidney transplantation, caused by an Rh(D) mismatch.
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