Howard E R, Garrett J R
Gut. 1970 Dec;11(12):1007-14. doi: 10.1136/gut.11.12.1007.
The ultrastructure of the myenteric nerves of colon and rectum removed from 10 children with Hirschsprung's disease has been studied and compared with normal infant bowel. Distal aganglionic (Hirschsprung) bowel often showed a rich supply of nerves within the muscle layers and there was no obvious morphological abnormality of constituent axons. The numbers of nerves diminished as more proximal parts of the bowel were examined and the fewest nerves were found where ganglia first appeared. These ganglia were similar in structure to the ganglia of normal bowel, and a striking feature of them all was the absence of collagen between constituent neuronal units. The larger nerve trunks of aganglionic bowel frequently contained myelinated axons and these have been observed within the myenteric plexus of normal rectum. This study supports previous histochemical investigations of the nerves in bowel from patients with Hirschsprung's disease and indicates that the condition is due to a complex and variable abnormality of the arrangement of the nervous tissue of the bowel wall, involving myenteric nerves as well as ganglia.
对10例患有先天性巨结肠症的儿童切除的结肠和直肠肌间神经的超微结构进行了研究,并与正常婴儿肠道进行了比较。远端无神经节(先天性巨结肠)肠段的肌层内神经供应往往丰富,组成轴突无明显形态异常。随着检查肠段向近端延伸,神经数量减少,在神经节首次出现的部位神经数量最少。这些神经节的结构与正常肠道的神经节相似,其一个显著特征是组成神经元单位之间没有胶原。无神经节肠段较大的神经干常含有有髓轴突,在正常直肠的肌间神经丛中也观察到了这些轴突。本研究支持先前对先天性巨结肠症患者肠道神经的组织化学研究,并表明该病是由于肠壁神经组织排列的复杂且可变的异常所致,涉及肌间神经以及神经节。