与先天性巨结肠(全结肠无神经节细胞症)并发的回肠闭锁  

Ileal atresia associated with Hirschsprung disease (total colonic aganglionosis)

作　　者：Gupta M. Beeram M.R. Pohl J.F. Custer M.D. 平智广 

机构地区：[1]Division of Pediatric Gastroenterology, Scott and White Memorial Hospital, Texas A and M University System Health Science Center, Temple, TX 76508, United States

出　　处：《世界核心医学期刊文摘（儿科学分册）》2006年第2期52-52,共1页

摘　　要：One of the most common causes of small bowel obstruction in newborns is ileal atresia, and one of the most common causes of colonic obstruction in neonates is aganglionic megacolon (Hirschsprung disease). However, atresias of the small intestinal tract associated with Hirschsprung disease are extremely rare. We describe an infant born with both ileal atresia and Hirschsprung disease. This is the 19th known report of the case of an infant who had ileal atresia associated with Hirschsprung disease.One of the most common causes of small bowel obstruction in newborns is ileal atresia, and one of the most common causes of colonic obstruction in neonates is aganglionic megacolon （Hirschsprung disease） . However, atresias of the small intestinal tract associated with Hirschsprung disease are extremely rare. We describe an infant bern with both ileal atresia and Hirschsprung disease. This is the 19th known report of the case of an infant who had ileal atresia associated with Hirschsprung disease.

关 键 词：先天性巨结肠 全结肠无神经节细胞症 回肠闭锁 并发 无神经节细胞性巨结肠 新生儿 小肠梗阻 大肠梗阻 小肠闭锁 

分 类 号：R656.9[医药卫生—外科学] R574.620.4[医药卫生—临床医学]