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婴儿期手术性黄疸

Surgical jaundice in infancy.

作者信息

Lilly J R

出版信息

Ann Surg. 1977 Nov;186(5):549-58. doi: 10.1097/00000658-197711000-00001.

Abstract

The surgery of congenital malformations of the biliary system has undergone a revolutionary change during the past decade. Although Kasai's hepatic portoenterostomy operation for biliary atresia is the most dramatic example, radical departures from conventional surgical treatment also have been advocated for choledochal cyst, Caroli's disease, congenital perforation of the bile ducts and biliary hypoplasia. This communication describes the lesions responsible for obstructive jaundice in the early months of life, briefly reviews standard treatment and consolidates the available information about the new operative procedures currently proposed for congenital anomalies of the biliary tract.

摘要

在过去十年中,胆道系统先天性畸形的外科手术经历了革命性的变革。尽管用于治疗胆道闭锁的Kasai肝门肠吻合术是最显著的例子,但对于胆总管囊肿、卡罗利病、先天性胆管穿孔和胆管发育不全,也有人主张彻底背离传统手术治疗方法。本文描述了导致生命早期梗阻性黄疸的病变,简要回顾了标准治疗方法,并整合了目前针对胆道先天性异常所提出的新手术方法的现有信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212b/1396306/28356e85b45e/annsurg00370-0010-a.jpg

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