先天性空回肠闭锁（附18例报告）  

CONGENITAL ATRESIA OF JEJUMUM AND ILEUM

作　　者：张乐进 吕秀芝[1] 张凯 

机构地区：[1]泰山医学院第一教学医院

出　　处：《泰山医学院学报》1995年第3期252-254,共3页Journal of Taishan Medical College

摘　　要：介绍１８例先天性空回肠闭锁的治疗，提出如病人情况允许应尽量行一期肠切除，斜端吻合术；对合并肠穿孔一般情况较差者，可行小肠端侧吻合，近端肠造口术，这样能提高患儿成活率。The present study is cincerned about the treament for 18 patients with congenital a-tresia of jcjumum and ilum. It is suggested 2that the primary cnterectomy and obligue end anstomosisshould be execuied as much as possible if the conitions of paticnts are permissivc.TO patients with enter-obrosis in bad conditions,intestinal end-to-side anstomosis and prximal ent rostomy should be operat-ed so that the subsistance rate can be raised.

关 键 词：先天性 空回肠 闭锁 新生儿 

分 类 号：R725.745.3[医药卫生—儿科]