Case Report: A case of immune hemolytic anemia after liver transplantation: passenger lymphocyte syndrome is the culprit.

Frontiers in transplantation Pub Date : 2024-08-26 eCollection Date: 2024-01-01 DOI:10.3389/frtra.2024.1463325
Qianzhe Zhao
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Abstract

Passenger lymphocyte syndrome (PLS) is most commonly observed after solid organ transplantation with minor ABO blood group incompatibility. It consists of a set of clinical symptoms brought on by the remaining lymphocytes of the donor organ developing antibodies against the recipient's antigens. Here, we describe a typical case of PLS in a type A+ recipient receiving a liver transplant from a type O+ donor. She suffered from jaundice, abnormally decreased hemoglobin level, and severe hemolytic anemia without bleeding. During hemolysis, we detected a positive direct antiglobulin test (DAT), and the thermal elution test revealed the presence of IgG anti-A antibodies in her serum. When immunosuppressive agents and blood transfusion were used together, cross-matched O+ washing red blood cells led to an expected outcome without side effects.

病例报告:一例肝移植后免疫性溶血性贫血:乘客淋巴细胞综合征是罪魁祸首。
乘客淋巴细胞综合征(PLS)最常见于ABO血型轻度不相容的实体器官移植后。它由供体器官残留的淋巴细胞产生针对受体抗原的抗体而引起的一系列临床症状组成。在这里,我们描述了一例典型的 PLS 病例,患者为 A+ 型,接受了来自 O+ 型供体的肝移植。她患有黄疸、血红蛋白水平异常降低和严重的溶血性贫血,但没有出血。在溶血过程中,我们检测到直接抗球蛋白试验(DAT)阳性,热洗脱试验显示她的血清中存在 IgG 抗 A 抗体。在同时使用免疫抑制剂和输血的情况下,交叉配型的 O+ 洗涤红细胞达到了预期效果,且无副作用。
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