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先天性胆道闭锁的病因:目前到底了解多少?

Aetiology of biliary atresia: what is actually known?

机构信息

Department of Pediatric Surgery, Hannover Medical School, Carl-Neuberg-Str, 1, 30625 Hannover, Germany.

出版信息

Orphanet J Rare Dis. 2013 Aug 29;8:128. doi: 10.1186/1750-1172-8-128.

Abstract

Biliary atresia (BA) is a rare disease of unknown etiology and unpredictable outcome, even when there has been timely diagnosis and exemplary surgery. It has been the commonest indication for liver transplantation during childhood for the past 20 years. Hence much clinical and basic research has been directed at elucidating the origin and pathology of BA. This review summarizes the current clinical variations of BA in humans, its occasional appearance in animals and its various manifestations in the laboratory as an experimental model.

摘要

先天性胆道闭锁(BA)是一种病因不明且预后不可预测的罕见疾病,即使及时诊断和进行了典范手术也是如此。在过去的 20 年中,它一直是儿童肝移植最常见的适应证。因此,许多临床和基础研究都致力于阐明 BA 的起源和病理学。本综述总结了人类 BA 的当前临床变异情况、在动物中的偶发表现以及作为实验模型在实验室中的各种表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c5e/3766137/4947e6ddc6ff/1750-1172-8-128-1.jpg

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