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先天性肥厚性幽门狭窄 被引量:1

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摘要 先天性肥厚性幽门狭窄为幽门环肌肥厚、增生使幽门管腔狭窄而引起的不完全梗阻,是新生儿常见的消化道畸形,仅次于肛门直肠畸形和先天性巨结肠.其发病率在不同地区和民族有很大差别,我国约为1/1000~1/3000.新生儿,较欧美少见.男性发病率远较女性高,约为4~8:1,原因不明.多见于第一胎.多为足月儿,早产儿少见.
作者 曹洪涛
出处 《中国乡村医生》 1998年第3期17-18,共2页
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  • 1褚珺,陈其民,施诚仁.先天性幽门肥厚性狭窄手术近期效果探讨[J].中华小儿外科杂志,2006,27(2):110-111. 被引量:15
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