胆道闭锁门肠造口术后长生存(21年)1例报告及并发症回顾

A. Tabari, A. Kidmas, A. Ogunseyinde, A. Samaila
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引用次数: 0

摘要

对于胆道闭锁,采用门肠造口术(Kasai手术)后长期存活数十年的患者是罕见的,并且门肠造口术与肝硬化的关联是众所周知的。与其他已知的常见肝硬化原因相比,对门肠造口所致肝硬化的影像学特征评价不甚重视。我们报告了一个尼日利亚的病例,出生时确诊胆道闭锁,在两个月大时进行的门肠造口手术存活了21年。肝硬化影像学表现为肝脏体积重分布明显,实质改变较少。该病例的长期生存率和影像学表现的肝硬化类型值得记录。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long survival ( 21 years) after portoenterostomy for biliary atresia: A case report and review of complications
Long term survival for decades after portoenterostomy (Kasai procedure) for biliary atresia is rare and the association of portoenterostomy with liver cirrhosis is well known. Not much attention was given in the evaluation of the imaging features of cirrhosis caused by portoenterostomy as received by other known usual causes of cirrhosis. We presented a case of a Nigerian with confirmed biliary atresia at birth, that suvived portoenterostomy performed at two months of age for 21years. The cirrhotic presentation at imaging was that of prominent volume redistribution with less parenchymal changes in the liver. The long term survival and the type of cirrhotic presentation on imaging in this case is worthy of note for the record.
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