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
收藏
页码：179 / 181
页数：3
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