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先天性巨结肠症，又称肠无神经节细胞症，是一种神经嵴细胞源性疾病和多基因遗传病，多见于新生儿及儿童，是新生儿低位肠梗阻常见病因之一。成人先天性巨结肠症合并巨大粪石临床上较为罕见。本研究通过回顾性分析本院2012年5月收治的1例成人先天性巨结肠合并粪石梗阻患者，探讨相关临床诊断，现报告如下。
成人先天性巨结肠症合并粪石梗阻1例
【摘 要】
：
先天性巨结肠症，又称肠无神经节细胞症，是一种神经嵴细胞源性疾病和多基因遗传病，多见于新生儿及儿童，是新生儿低位肠梗阻常见病因之一。成人先天性巨结肠症合并巨大粪石临床上较
【机 构】
：
武警总医院普外科
【出 处】
：
实用临床医药杂志
【发表日期】
：
2014年E02期
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