摘要
先天性巨结肠(Hirschsprungdisease,HD)是以便秘为主要临床表现的一种常见的消化道畸形.病因为外胚层神经嵴细胞迁移发育过程停顿.病变肠壁肌间神经丛和黏膜下神经丛的神经节细胞缺如。使肠段失去正常蠕动(即间歇性收缩和松弛的推进式运动)而处于经常的痉挛状态,造成粪便排出障碍.近端肠管则被动继发扩张,异常扩大、肥厚,形成所谓的巨结肠。
出处
《中华胃肠外科杂志》
CAS
北大核心
2011年第10期751-752,共2页
Chinese Journal of Gastrointestinal Surgery
参考文献14
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同被引文献8
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二级引证文献6
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