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遗传性出血性毛细血管扩张症肝动静脉畸形的肝移植治疗

Liver transplantation for hepatic arteriovenous malformation in hereditary haemorrhagic telangiectasia.

作者信息

Bauer T, Britton P, Lomas D, Wight D G, Friend P J, Alexander G J

机构信息

Department of Medicine, Clinical School of Medicine, University of Cambridge, Addenbrooke's NHS Trust, UK.

出版信息

J Hepatol. 1995 May;22(5):586-90. doi: 10.1016/0168-8278(95)80455-2.

Abstract

Symptomatic hepatic involvement is a rare complication of hereditary hemorrhagic telangiectasia and most commonly consists of fibrosis or cirrhosis. We describe a 33-year-old woman in whom multiple hepatic arteriovenous malformations led to high output cardiac failure and liver failure due to biliary necrosis with refractory biliary sepsis, requiring orthotopic liver transplantation. Hepatic arteriovenous malformations were the first manifestation of the disease and a similar asymptomatic hepatic tumour was subsequently detected in her 60-year-old father who also had the classical cutaneous stigmata of the syndrome. Unrecognised genetic factors may determine the clinical spectrum of hereditary haemorrhagic telangiectasia including the hepatic manifestations.

摘要

症状性肝脏受累是遗传性出血性毛细血管扩张症的一种罕见并发症,最常见的表现为纤维化或肝硬化。我们报告一名33岁女性,其多处肝动静脉畸形导致高输出量心力衰竭和肝功能衰竭,原因是胆汁性坏死伴难治性胆源性败血症,需要进行原位肝移植。肝动静脉畸形是该疾病的首发表现,随后在她60岁的父亲身上也检测到了类似的无症状肝脏肿瘤,她的父亲也有该综合征的典型皮肤体征。未被认识的遗传因素可能决定遗传性出血性毛细血管扩张症的临床谱,包括肝脏表现。

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