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慢性肠道假性梗阻。27例报告及文献复习

Chronic intestinal pseudo-obstruction. A report of 27 cases and review of the literature.

作者信息

Schuffler M D, Rohrmann C A, Chaffee R G, Brand D L, Delaney J H, Young J H

出版信息

Medicine (Baltimore). 1981 May;60(3):173-96.

PMID:6894476
Abstract

Twenty-seven cases of chronic intestinal pseudo-obstruction are reported. The causes of pseudo-obstruction were progressive systemic sclerosis in 14, hollow visceral myopathy in 4, visceral neuropathy in 2, sclerosing mesenteritis in 1, and jejunal diverticulosis in 1. No identifiable cause was found in five. Chronic pseudo-obstruction is a long-term illness characterized by vomiting, abdominal distention, abdominal pain and weight loss. Involvement is often present throughout the intestine so that patients may present with a variety of symptoms deriving from the esophagus, stomach, small intestine, and colon. Hollow visceral myopathy and visceral neuropathy are usually familial and urologic involvement is sometimes present in the former. Abnormalities of smooth muscle function can be discerned by radiography and esophageal manometry. The pattern and distribution of the abnormalities are helpful in differentiating pseudo-obstruction from true mechanical obstruction. They may also be helpful in differentiating one form of pseudo-obstruction from another. The majority of cases have identifiable pathology within either the smooth muscle or myenteric plexus of the bowel wall. The natural history of pseudo-obstruction is variable. Remissions and exacerbations occur and may be unrelated to anything that is done therapeutically. The illness is unresponsive to any drug known to have an effect on intestinal motility. Antibiotic treatment of small intestinal bacterial overgrowth and selected surgical procedures may occasionally be palliative. Many patients develop malnutrition and require home parenteral nutrition in order to survive.

摘要

本文报告了27例慢性肠道假性梗阻病例。假性梗阻的病因包括进行性系统性硬化症14例、中空脏器肌病4例、内脏神经病变2例、硬化性肠系膜炎症1例、空肠憩室病1例。5例未发现明确病因。慢性假性梗阻是一种以呕吐、腹胀、腹痛和体重减轻为特征的长期疾病。病变常累及整个肠道,因此患者可能出现源自食管、胃、小肠和结肠的各种症状。中空脏器肌病和内脏神经病变通常具有家族性,前者有时会累及泌尿系统。通过放射学检查和食管测压可发现平滑肌功能异常。这些异常的模式和分布有助于鉴别假性梗阻与真正的机械性梗阻,也有助于区分不同类型的假性梗阻。大多数病例在肠壁的平滑肌或肌间神经丛内有可识别的病理改变。假性梗阻的自然病程各异,会出现缓解和加重,且可能与任何治疗措施无关。该疾病对任何已知对肠道蠕动有影响的药物均无反应。针对小肠细菌过度生长的抗生素治疗和某些手术操作偶尔可能起到缓解作用。许多患者会出现营养不良,需要家庭肠外营养以维持生命。

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