Double duodenal atresia noticed as an intraabdominal cyst in the fetus

被引：6

作者：

Migita, Misato ^{[1
]}

Watanabe, Toshihiko ^{[1
]}

Sato, Kaori ^{[1
]}

Ohno, Michinobu ^{[1
]}

Takahashi, Masataka ^{[1
]}

Takezoe, Toshiko ^{[1
]}

Shimizu, Takahiro ^{[1
]}

Yoshida, Akio ^{[2
]}

Fujinaga, Hideshi ^{[2
]}

Ito, Yushi ^{[2
]}

Sugibayashi, Rika ^{[3
]}

Sumie, Masahiro ^{[3
]}

Wada, Seiji ^{[3
]}

Sago, Haruhiko ^{[3
]}

Fuchimoto, Yasushi ^{[1
]}

Kanamori, Yutaka ^{[1
]}

机构：

[1] Natl Ctr Child Hlth & Dev, Dept Surg Specialties, Div Surg, Setagaya Ku, 2-10-1 Okura, Tokyo 1578535, Japan

[2] Natl Ctr Child Hlth & Dev, Ctr Maternal Fetal Neonatal & Reprod Med, Div Neonatol, Setagaya Ku, Tokyo 1578535, Japan

[3] Natl Ctr Child Hlth & Dev, Ctr Maternal Fetal Neonatal & Reprod Med, Div Fetal Med, Setagaya Ku, Tokyo 1578535, Japan

来源：

JOURNAL OF PEDIATRIC SURGERY CASE REPORTS | 2014年 / 2卷 / 04期

关键词：

Duodenal atresia; Fetal diagnosis; Polyhydramnios;

D O I：

10.1016/j.epsc.2014.03.016

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Double duodenal atresia is a rare disease and twenty-two cases have been reported in the English literature. We report here a case of double duodenal atresia that had been suspected by fetal ultrasonography as polyhydramnios and a large cyst at the right upper abdomen. Two membranous diaphragms at the duodenum separated the duodenal lumen and formed a cystic lesion. Surgical reconstruction was performed. (C) 2014 The Authors. Published by Elsevier Inc. All rights reserved.

引用

页码：200 / 202

页数：3

共 13 条

[1] CONGENITAL DUODENAL OBSTRUCTION [J].