医学
假性肠梗阻
胃肠病学
硫唑嘌呤
病理
泼尼松龙
纤维化
内科学
疾病
作者
P A Hill,Karen M. Dwyer,David A. Power
出处
期刊:Lupus
[SAGE]
日期:2000-07-01
卷期号:9 (6): 458-463
被引量:46
标识
DOI:10.1191/096120300678828505
摘要
We report the case of a woman with systemic lupus erythematosus initially manifesting with fever, rash and arthritis, and two years later with Class IV lupus nephritis. Following treatment with cyclophosphamide she developed symptoms and signs of chronic intestinal pseudo-obstruction (CIPO) that was initially thought to be due to a neutropenic enterocolitis. However, persistence of symptoms resulted in segmental resection of the ileum which showed widespread myocyte necrosis and active inflammation within the muscularis propria. A subsequent, more extensive ileocolic resection showed severe diffuse atrophy and fibrosis of the muscularis propria throughout the resected bowel. The absence of mesenteric vasculitis and the clinical response of the CIPO to the immunosupressive regimen of prednisolone and cyclosporin A suggest that the bowel muscle coat changes reflect an intestinal myopathy secondary to systemic lupus erythematosus, and may have an auto-immune etiology.
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