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先天性胆道畸形患者的内镜治疗方法。

Endoscopic approach to the patient with congenital anomalies of the biliary tract.

作者信息

Liu Quin Y, Nguyen Vivien

机构信息

Keck School of Medicine, University of Southern California, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA.

出版信息

Gastrointest Endosc Clin N Am. 2013 Apr;23(2):505-18. doi: 10.1016/j.giec.2012.12.004. Epub 2013 Jan 17.

Abstract

Congenital biliary tract anomalies typically present with neonatal cholestasis. In children and adults, endoscopic retrograde cholangiopancreatography (ERCP) and endoscopic ultrasound are used to evaluate and treat choledochal cysts. Contrarily, endoscopy has traditionally played a minor role in the diagnosis of the cholestatic infant. Recent studies support the incorporation of ERCP into the diagnostic algorithm for biliary atresia and neonatal cholestasis. But at present, most pediatric liver centers do not consider its use essential. This article reviews the congenital biliary tract anomalies in which endoscopy has been shown to contribute to the evaluation of the cholestatic infant.

摘要

先天性胆道异常通常表现为新生儿胆汁淤积。对于儿童和成人,内镜逆行胰胆管造影(ERCP)和内镜超声用于评估和治疗胆总管囊肿。相反,传统上内镜检查在胆汁淤积婴儿的诊断中作用较小。最近的研究支持将ERCP纳入胆道闭锁和新生儿胆汁淤积的诊断流程。但目前,大多数儿科肝脏中心并不认为其使用是必不可少的。本文综述了已证明内镜检查有助于评估胆汁淤积婴儿的先天性胆道异常。

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