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先天性肝纤维化:诊断与外科治疗要点

Congenital hepatic fibrosis: aspects of diagnosis and surgical management.

作者信息

Sokhi G S, Morrice J J, McGee J O, Blumgart L H

出版信息

Br J Surg. 1975 Aug;62(8):621-3. doi: 10.1002/bjs.1800620809.

Abstract

Five cases of congenital hepatic fibrosis are described. In all the patients the diagnosis was delayed as a result of either failure to perform liver biopsy or misinterpretation of the histological features. Four patients had multiple operations for the control of haematemesis or the relief of portal hypertension. It is stressed that a high index of suspicion, the use of endoscopy and a liver biopsy are essential to avoid delay in diagnosis. The patients have a good prognosis provided that the diagnosis is established at an early stage and portacaval anastomosis performed.

摘要

本文描述了5例先天性肝纤维化患者。由于未进行肝活检或对组织学特征解读错误,所有患者的诊断均被延误。4例患者接受了多次手术以控制呕血或缓解门静脉高压。强调高度的怀疑指数、内镜检查的应用和肝活检对于避免诊断延误至关重要。如果能在早期确诊并进行门腔静脉吻合术,患者预后良好。

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