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抗磷脂综合征患者的肝移植:一例报告

Liver Transplantation in a Patient With Antiphospholipid Syndrome: A Case Report.

作者信息

Steckelberg Rachel C, Antongiorgi Zarah D, Steadman Randolph H

机构信息

From the Department of Anesthesiology and Perioperative Medicine, University of California Los Angeles, Los Angeles, California.

出版信息

A A Case Rep. 2017 Sep 1;9(5):148-150. doi: 10.1213/XAA.0000000000000551.

Abstract

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.

摘要

抗磷脂综合征(APS)是一种获得性血栓形成倾向疾病,其特征为存在针对细胞膜磷脂的自身抗体。虽然凝血功能改变会使终末期肝病复杂化,但很少有报告描述患有如APS等既往存在的高凝性疾病的肝移植受者的围手术期管理。我们报告一名有APS病史、布加综合征合并肝硬化、肝肺综合征和肝素诱导的血小板减少症的患者,该患者接受肝移植后并发肝动脉血栓形成。管理措施包括术后使用Xa因子抑制剂进行抗凝,在再次移植后,过渡到长期抗凝治疗并最终康复。

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