Newborn male presented with congenital diaphragmatic hernia and choledochal cyst: A case report

被引：1

作者：

Krebs, Daniel ^{[1
]}

Herman, Richard S. ^{[2
]}

Blewett, Christopher ^{[2
]}

机构：

[1] Univ Mississippi, Med Ctr, Jackson, MS 39232 USA

[2] Univ Mississippi, Med Ctr, Div Pediat Surg, Jackson, MS 39232 USA

来源：

JOURNAL OF PEDIATRIC SURGERY CASE REPORTS | 2015年 / 3卷 / 05期

关键词：

Congenital diaphragmatic hernia; Choledochal cyst; Congenital anomalies;

D O I：

10.1016/j.epsc.2015.03.001

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Infants with congenital diaphragmatic hernia (CDH) have an increased incidence of associated malformations, ranging from 10% to 50% higher than the general population [1-5]. Choedochal cysts, congenital cystic dilations of the biliary tree, are anomalies that have not yet been described in association with CDH. We describe a patient with a left congenital diaphragmatic hernia who was later diagnosed with a choledochal cyst. (C) 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

引用

页码：179 / 181

页数：3

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