先天性门静脉缺失:明确门静脉分流,避免肝移植。

Canadian liver journal Pub Date : 2021-08-09 eCollection Date: 2021-01-01 DOI:10.3138/canlivj-2020-0011
Noémie Laverdure, Michel Lallier, Josée Dubois, Massimiliano Paganelli
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引用次数: 2

摘要

肝移植历来被推荐用于先天性门静脉缺失伴肝外先天性门静脉系统分流的患者。在此,基于一名2岁女孩的病例报告和对1974年至2020年所有已发表病例的全面回顾,我们发现这种诊断通常隐藏了发育不良的门静脉,通过关闭分流器成功地重新渗透门静脉,以重建生理血管解剖。这强调了通过球囊闭塞试验对肝外先天性门系统分流进行详细解剖描述的重要性,以便计划最佳手术方法并避免不必要的肝移植。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Congenital absence of the portal vein: Define the portosystemic shunt, avoid liver transplantation.

Congenital absence of the portal vein: Define the portosystemic shunt, avoid liver transplantation.

Liver transplantation has been historically recommended for patients with congenital absence of the portal vein associated with extrahepatic congenital portosystemic shunts. Here, based on a case report of a 2-year-old girl and a thorough review of all published cases from 1974 to 2020, we show that such a diagnosis most often conceals a hypoplastic portal vein, which can be successfully re-permeabilized through the closure of the shunt in order to re-establish a physiological vascular anatomy. This highlights the importance of achieving a detailed anatomical description of extrahepatic congenital portosystemic shunts with a balloon occlusion test in order to plan the best surgical approach and avoid unnecessary liver transplantation.

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