抗磷脂综合征患者肝移植一例报告。

Rachel C Steckelberg, Zarah D Antongiorgi, Randolph H Steadman
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引用次数: 3

摘要

抗磷脂综合征(APS)是一种以细胞膜磷脂自身抗体为特征的获得性血栓性疾病。虽然凝血功能改变可使终末期肝病复杂化,但很少有报道描述先前存在高凝障碍(如APS)的肝移植受者的围手术期管理。我们报告了一位有APS、Budd-Chiari综合征合并肝硬化、肝肺综合征和肝素诱导的血小板减少症病史的患者,他接受了肝移植并肝动脉血栓形成。治疗包括术后使用Xa因子抑制剂进行抗凝治疗,并在重复移植后转入长期抗凝治疗并最终恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Liver Transplantation in a Patient With Antiphospholipid Syndrome: A Case Report.

Antiphospholipid syndrome (APS) is an acquired thrombophilic disorder characterized by autoantibodies to cell membrane phospholipids. While altered coagulation can complicate end-stage liver disease, there are few reports describing the perioperative management for liver transplantation in recipients with a preexisting hypercoagulable disorder, such as APS. We present a patient with a history of APS, Budd-Chiari syndrome with cirrhosis, hepatopulmonary syndrome, and heparin-induced thrombocytopenia who underwent liver transplantation complicated by hepatic artery thrombosis. Management included postoperative anticoagulation with a factor Xa inhibitor and, after repeat transplantation, transition to long-term anticoagulation therapy with eventual recovery.

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