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一名混合性结缔组织病患者出现自发性气腹并伴有肠壁囊样积气。

Spontaneous pneumoperitoneum with Pneumatosis cystoides intestinalis in a patient with mixed connective tissue disease.

作者信息

Samach M, Brandt L J, Bernstein L H

出版信息

Am J Gastroenterol. 1978 Apr;69(4):494-500.

PMID:685959
Abstract

Pneumatosis cystoides intestinalis (PCI), a disorder in which gas filled cysts develop within the bowel wall, has been associated with collagen vascular disease, usually progressive systemic sclerosis (PSS). We have extended the spectrum of collagen vascular disease associated with PCI by this report of a patient with mixed connective tissue disease (MCTD) who developed PCI and recurrent spontaneous pneumoperitoneum (SP). Possible pathogenetic mechanisms are reviewed and the management of the asymptomatic patient with pneumoperitoneum, PCI and collagen vascular disease is discussed.

摘要

肠壁囊样积气症(PCI)是一种在肠壁内形成充满气体囊肿的病症,它与胶原血管病有关,通常是进行性系统性硬化症(PSS)。通过本报告中一名患有混合性结缔组织病(MCTD)并发生PCI和复发性自发性气腹(SP)的患者,我们扩展了与PCI相关的胶原血管病谱。本文回顾了可能的发病机制,并讨论了对患有气腹、PCI和胶原血管病的无症状患者的管理。

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