Annular pancreas in identical twin newborns

被引：6

作者：

Kumar, Rajiv B. ^{[1
]}

Hulvat, Melissa C. ^{[1
]}

Newman, Barry M. ^{[1
]}

Muraskas, Jonathan K. ^{[1
]}

机构：

[1] Loyola Univ, Med Ctr, Stritch Sch Med, Maywood, IL 60153 USA

来源：

JOURNAL OF PEDIATRIC SURGERY | 2006年 / 41卷 / 08期

关键词：

annular pancreas; duodenal obstruction; duodenal stenosis; intestinal atresia; monozygotic twins;

D O I：

10.1016/j.jpedsurg.2006.04.028

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Annular pancreas is a rare congenital anomaly occurring in 1 of every 12,000 to 15,000 live births [Nerwich N, Shi E. Neonatal duodenal obstruction: a review of 30 consecutive cases. Pediatr Surg Int 1994;9:47-50]. It may remain asymptomatic throughout life, present in adulthood, or present in infancy as a high intestinal obstruction. Review of the literature demonstrates only 8 cases of familial annular pancreas and no case of twins exhibiting the disease. We will describe a case of identical (monochorionic diamniotic) female twins with neonatal presentation of duodenal obstruction and annular pancreas, find discuss data supportive of a genetic etiology. (c) 2006 Elsevier Inc. All rights reserved.

引用

页码：e19 / e21

页数：3

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