Perinatally discovered complete tubular colonic duplication associated with anal atresia

被引：12

作者：

Jellali, Mohamed A. ^{[1
]}

Mekki, Mongi ^{[2
]}

Saad, Jamel ^{[1
]}

Zrig, Ahmed ^{[1
]}

Elanes, Imene ^{[2
]}

Mnari, Walid ^{[1
]}

Maatouk, Mezri ^{[1
]}

Harzallah, Wissem ^{[1
]}

Toumi, Samir ^{[3
]}

Krichene, Imed ^{[2
]}

Salem, Randa ^{[1
]}

Nouri, Abdellatif ^{[2
]}

Golli, Mondher ^{[1
]}

机构：

[1] CHU Fattouma Bourguiba, Dept Radiol, Monastir 5000, Tunisia

[2] CHU Fattouma Bourguiba, Dept Pediat Surg, Monastir 5000, Tunisia

[3] CHU Fattouma Bourguiba, Dept Anaesthesia & Chirurg Intens, Monastir 5000, Tunisia

来源：

JOURNAL OF PEDIATRIC SURGERY | 2012年 / 47卷 / 06期

关键词：

Duplication; Colon; Anal atresia; Children; Malformation; SQUAMOUS-CELL CARCINOMA; NEWBORN; BLADDER; RECTUM; ILEUM; ANUS;

D O I：

10.1016/j.jpedsurg.2012.01.082

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Complete tubular colonic duplication (CTCD) is exceedingly rare. The association of CTCD with an anorectal malformation is unusual. This malformation may be found unexpectedly at laparotomy. We present 3 cases of surgically proven neonate CTCD discovered at laparotomy for anal atresia. We reviewed the mode of clinical presentation, the imaging, and laparotomy findings. Our series illustrates that this rare disease presents perinatally in association with anal atresia, with or without other associated anomalies. (C) 2012 Elsevier Inc. All rights reserved.

引用

页码：E19 / E23

页数：5