乘客淋巴细胞综合征--肝移植后贫血的不寻常原因

IF 3.7 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Annals of hepatology Pub Date : 2024-02-01 DOI:10.1016/j.aohep.2024.101469
Alejandro Gutierrez-Castillo , Héctor Cabrera-Larios , Fernando Segovia-Rivera , Rafael Valdez-Ventura , Nayelli C. Flores-García
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引用次数: 0

摘要

导言和目的肝移植术后贫血的发生率从 4.3% 到 28.2% 不等。最初两周内出现贫血的原因包括出血、败血症、药物和溶血。免疫性溶血占不到 1%,包括移植物抗宿主病和 ABO 不相容引起的溶血。材料和患者一名 43 岁的女性,血型 A+,有 HCV 相关性肝硬化和 BCLC-A 型肝细胞癌病史,被选中进行肝移植。手术顺利,只需输注一个 O+ 血型单位。术后进展顺利,未出现并发症。移植后第 10 天,她出现血红蛋白下降 3 克/分升、白细胞增多、急性期反应物升高和混合型高胆红素血症。食管胃十二指肠镜和结肠镜检查显示没有活动性出血。溶血谱显示血红蛋白值下降,DHL升高,Coombs阴性,无血吸虫。患者要求进行 MRCP 检查,但没有发现胆汁渗漏或活动性出血。由于怀疑是药物引起的溶血,他克莫司被改为霉酚酸酯;由于可能是败血症引起的溶血,增加了广谱抗生素治疗,但情况没有改善。第 14 天,怀疑出现一过性淋巴细胞综合征。要求检测异血凝素水平,结果呈阳性,于是输了两个 O+ 血单位。结果 在我们处理肝移植后溶血性贫血的过程中,最初出现了两种理论:1)他克莫司引起的溶血,因此暂停使用并改用霉酚酸酯;2)败血症引起的溶血,原因是白细胞增多和炎症,因此开始使用美罗培南和万古霉素。但两次干预后病情均无好转。最后,由于怀疑是一过性淋巴细胞综合征,她被要求进行异血凝素检测,结果呈阳性,在输注了 2 个含有抗 A+ 抗体的 O+ 血单位后,她的病情有所好转,确诊了这一病症。心肺移植的发病率较高,其次是肝移植。供体和受体的ABO血型不匹配也会增加发病风险,O型供体和A型受体的发病率较高(61%),其次是O型供体和B型受体(22%)。临床表现以发热、腹泻、皮疹和溶血为特征。溶血通常发生在肝移植后的第3至24天,往往是轻微和自限性的。当受体的直接抗球蛋白检测呈阳性,且血清中存在针对受体红细胞抗原的供体抗体时,即可确诊。治疗方法包括输注 O 型红细胞单位,在严重溶血的情况下,可使用免疫抑制剂或血浆置换术。
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Passenger lymphocyte syndrome, an unusual cause of anemia after liver transplantation

Introduction and Objectives

The prevalence of anemia after liver transplantation ranges from 4.3% to 28.2%. Causes that occur in the first two weeks include bleeding, sepsis, medications, and hemolysis. Immune hemolysis represents less than 1% of the cases and includes graft-versus-host disease and hemolysis associated with ABO incompatibility. We present a case of passenger lymphocyte syndrome as a cause of immune hemolytic anemia two weeks after a liver transplant.

Materials and Patients

A 43-year-old woman, blood group A+, with a history of HCV-related liver cirrhosis and BCLC-A hepatocellular carcinoma, was chosen for a liver transplant. Surgery was uneventful, requiring the transfusion of an O+ blood unit. The postoperative evolution was carried out without complications. On day 10, after the transplant, she presented a drop of 3 g/dL in hemoglobin, leukocytosis, elevated acute phase reactants, and mixed hyperbilirubinemia. An esophagogastroduodenoscopy and colonoscopy showed no active bleeding. The hemolysis profile showed a decrease in the haptoglobin value and an increase in DHL, negative Coombs, without schistocytes. An MRCP was requested, with no evidence of bile leakage or active bleeding. Because of the suspicion of hemolysis due to drugs, tacrolimus was changed to mycophenolate mofetil, and because of possible hemolysis due to sepsis, broad-spectrum antibiotic coverage was added without improvement. On day 14, there was a suspicion of transient lymphocyte syndrome. Isohemagglutinin levels were requested and became positive, and two O+ blood units were transfused. The following day, she presented a significant improvement in all laboratory parameters, and on day 20 she was discharged from the hospital without any abnormality in her laboratory parameters.

Results

In our management of hemolytic anemia after liver transplantation, two theories initially emerged: 1) Hemolysis due to tacrolimus, for which it was suspended and changed to mycophenolate mofetil, and 2) Hemolysis due to sepsis, due to leukocytosis and inflammation, initiating coverage with meropenem and vancomycin. But without improvement after both interventions. Finally, due to suspicion of transient lymphocyte syndrome, isohemagglutitins were requested and were positive, and after the transfusion of 2 O+ blood units, containing anti-A+ antibodies, she showed improvement, confirming the diagnosis.

Conclusions

In the passenger lymphocyte syndrome, there is a donor B lymphocyte production of antibodies causing a primary or secondary response to recipient erythrocytes. The incidence is higher in the heart-lung transplant, followed by liver transplantation. The risk also increases according to the donor-recipient ABO mismatch, being more common with group O donors and group A recipient (61%), followed by group O donors and group B recipients (22%). The clinical picture is characterized by fever, diarrhea, rash and hemolysis. The hemolysis usually occurs on days 3 to 24 after the liver transplantation and tends to be mild and self-limited. The diagnosis is made when the recipient had a positive direct antiglobulin test and there were donor antibodies in the serum against the recipient's red blood cell antigens. Treatment options include the transfusion of O red blood cell units and, in cases of severe hemolysis, immunosuppressors or plasmapheresis.

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来源期刊
Annals of hepatology
Annals of hepatology 医学-胃肠肝病学
CiteScore
7.90
自引率
2.60%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Annals of Hepatology publishes original research on the biology and diseases of the liver in both humans and experimental models. Contributions may be submitted as regular articles. The journal also publishes concise reviews of both basic and clinical topics.
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Editorial board Global multi-societies endorsement of the MAFLD definition An Acknowledgement Biological aging accelerates hepatic fibrosis: Insights from the NHANES 2017-2020 and genome-wide association study analysis. Development of a biodegradable prosthesis through tissue engineering, for the organ-replacement or substitution of the extrahepatic bile duct
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