胆囊复制

Bhaskar Chintakayala
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引用次数: 0

摘要

胆道结构的异常解剖,如胆囊复制是发生在1:3800 - 4000新生儿中的罕见表现之一[1]。在腹腔镜胆囊切除术等手术干预中,这些先天性异常会造成胆道损伤的明确风险。术前需要精确的诊断,以确定精确的治疗计划,并确保完全切除两个胆囊,无并发症。由于这些异常通常与胆汁引流不足引起的结石形成有关。腹腔镜胆囊切除术是治疗的首选。摘要
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Duplication of Gallbladder
Aberrant anatomy of biliary structures like duplication of gallbladder is one of the rare presentations occurring in 1:38004000 births [1]. These congenital anomalies pose a definite risk of biliary injury during operative interventions like laparoscopic cholecystectomy. Precise diagnosis pre-operatively is required for precise plan of management and to make sure both the gallbladders are removed completely without complications. As these anomalies are frequently associated with stone formation due to inadequate bile drainage. Laparoscopic cholecystectomy is the treatment of choice. Abstract
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