先天性神经节性巨结肠;巨结肠病。

J. F. Mokrohisky, G. Keefer
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引用次数: 3

摘要

1887年,在Hirschsprung对两名患有先天性巨结肠的患者进行全面分析后,先天性巨结肠被认为是一种临床实体。直到几年前,“巨结肠病”这个术语还被用来描述那些没有明显器质性原因的患者的结肠肿大。1920年,Dalla Valle首次对一名先天性巨结肠病患者的结肠神经节细胞进行了全面研究。他报告说,在扩张结肠远端狭窄的肠段中没有神经节细胞。1949年,Neuhauser描述了一种钡灌肠检查技术,用于显示狭窄的神经节段。在这一值得注意的贡献之后,Swenson描述了一种手术技术,用于切除异常节段并恢复肠的连续性,同时保留肛门括约肌。在这次展览中,特别强调的是x线摄影表现的变化
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Congenital aganglionic megacolon; Hirschsprung's disease.
CONGENITAL megacolon was recognized as a clinical entity in 1887, following Hirschsprung's comprehensive analysis of two patients with this disease. Up until a few years ago the term "Hirschsprung's disease" had been used to describe enlargement of the colon in those patients not having demonstrable organic cause for their megacolon. In 1920 the first comprehensive study of the ganglion cells of a colon from a patient with Hirschsprung's disease was made by Dalla Valle. He reported the absence of ganglion cells in the narrowed segment of bowel distal to the dilated colon. In 1949 Neuhauser described a technique of barium-enema examination for demonstrating the narrowed, aganglionic segment. Following this noteworthy contribution, Swenson described an operative technique for removal of the abnormal segment and restoration of the continuity of the bowel with preservation of the anal sphincters. In this exhibit, special emphasis is directed to the variations in the roentgenographic appearances
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