Cohen S
Scand J Gastroenterol Suppl. 1982;71:125-31.
Autonomic dysfunction leads to a variety of clinical disorders involving all parts of the gut. These neural disorders are distinct from the four other recognised categories of disorders involving myogenic function, myoelectric activity, hormonal regulation and abnormal humoral factors. Criteria for establishing that a disorder has a neurogenic aetiology vary in different diseases. Absence of a neural mediated response with intact muscle function has been the major criterion used in most studies. Neural mediated responses of peristalsis, sphincteric relaxation and intestinal contraction following distension or feeding are the major parameters of assessment. Abnormalities in neural function have been demonstrated in achalasia, symptomatic diffuse oesophageal spasm, diabetes mellitus, amyloidosis, scleroderma and chronic idiopathic intestinal pseudoobstruction. The anatomical site and type of gut neurological disorder varies in each condition. Morphological studies have been helpful in demonstrating specific intranuclear inclusion bodies in some pseudoobstruction patients, and vagal and ganglionic lesions in achalasia. Intact muscle ad myoelectric function as well as normal responsiveness to drugs acting directly upon muscle may be established by morphological study. Advancement in basic technology should provide a rewarding area for future study of the pathogenesis and treatment of the gut neurological disorders.
自主神经功能障碍会引发涉及肠道各个部位的多种临床病症。这些神经紊乱与其他四类已被认可的涉及肌源性功能、肌电活动、激素调节及异常体液因素的病症有所不同。在不同疾病中,确定一种病症具有神经源性病因的标准各不相同。在大多数研究中,主要标准是在肌肉功能完好的情况下缺乏神经介导反应。扩张或进食后蠕动、括约肌松弛及肠收缩的神经介导反应是主要的评估参数。在贲门失弛缓症、症状性弥漫性食管痉挛、糖尿病、淀粉样变性、硬皮病及慢性特发性假性肠梗阻中已证实存在神经功能异常。在每种病症中,肠道神经紊乱的解剖部位和类型各不相同。形态学研究有助于在一些假性肠梗阻患者中发现特定的核内包涵体,以及在贲门失弛缓症中发现迷走神经和神经节病变。通过形态学研究可确定肌肉和肌电功能完好,以及对直接作用于肌肉的药物具有正常反应性。基础技术的进步应为未来肠道神经紊乱的发病机制和治疗研究提供一个有价值的领域。