A Case of Prune Belly Syndrome

被引：6

作者：

Xu, Wei ^{[1
]}

Wu, Hui ^{[1
]}

Wang, Dong-Xuan ^{[2
]}

Mu, Zhi-Hong ^{[1
]}

机构：

[1] Jilin Univ, Dept Neonatol, Hosp 1, Changchun 130021, Peoples R China

[2] Jilin Univ, Dept Ultrason Diag, Hosp 1, Changchun 130021, Peoples R China

来源：

PEDIATRICS AND NEONATOLOGY | 2015年 / 56卷 / 03期

关键词：

abdominal wall musculature deficiency; bilateral cryptorchidism; prune belly syndrome; urinary tract anomalies; OF-THE-LITERATURE; TRIAD SYNDROME; CHILDREN; OBSTRUCTION;

D O I：

10.1016/j.pedneo.2013.03.014

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Prune belly syndrome (PBS) is a rare congenital disorder characterized by deficient abdominal wall muscles, urinary tract malformation, and, in males, cryptorchidism. We present a case of PBS in China. The patient was a newborn baby boy who had wrinkled, "prune-like" abdominal skin, bilateral cryptorchidism, and urinary system malformation, complicated with hypoplasia of the lung and branch of the coronary artery-right ventricular fistula. His kidney function was inadequate. The patient subsequently died at age 28 days due to septicemia from a severe urinary tract infection. Copyright (C) 2013, Taiwan Pediatric Association. Published by Elsevier Taiwan LLC. All rights reserved.

引用

页码：193 / 196

页数：4

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