Okuda Y, Takasugi K, Imai A, Kondo Y, Hachinota M, Ueda S, Nitta M
Center for Rheumatic Diseases, Dohgo Spa Hospital, Matsuyama-city.
Ryumachi. 1990 Oct;30(5):403-7, 408; discussion 407-8.
Episodes of catastrophic entero-colitis associated with mesenteric vascular insufficiency in patients with rheumatoid arthritis(RA) have rarely been recorded thus far. We herein report two cases of RA complicated with severe attacks of entero-colitis presumably due to mesenteric vasculitis. Surgical intervention was necessary in the first case, while the second patient recovered well only through conservative therapy. Case 1: A 74-year-old man with history of RA since 1985 started to complain of abdominal discomfort and nausea early in February, 1989. On February 12, Episodes of tarry stool developed. Rapid down-hill clinical course prompted laparotomy under the clinical diagnosis of peritonitis. Ischemic changes were observed at the ileum end, the entire length of which was 120 cm orally from the cecum. The site was resected. Multiple linear and aphthoid ulcer lesions were discovered throughout the entire lumen. Histopathologically, evidence of necrotizing vasculitis such as fibrinoid necrosis and mural thrombi was demonstrated in small arteries of the submucosal layer underlying the ulcer lesion. Case 2: A 63-year-old woman who had been suffering from RA since 1980 noticed the onset of nausea, abdominal pain and bloody diarrhea in July, 1989. Colonoscopy examination revealed multiple linear and aphthoid ulcers in the sigmoid colon which was presumed to be due to ischemia. Laboratory evaluation at that time demonstrated hypocomplementemia, positive circulating immune complex and high titer of anti-DNA antibody. Corticosteroid therapy with moderate dose was successful in alleviation of all the abnormal findings and the patient fully recovered three months after her initial GI episode.
迄今为止,类风湿关节炎(RA)患者中与肠系膜血管供血不足相关的灾难性小肠结肠炎病例鲜有记录。我们在此报告两例RA合并严重小肠结肠炎发作的病例,推测病因是肠系膜血管炎。第一例患者需要手术干预,而第二例患者仅通过保守治疗就康复良好。病例1:一名74岁男性,自1985年起患有RA,1989年2月初开始出现腹部不适和恶心。2月12日,出现柏油样便。病情迅速恶化促使在腹膜炎临床诊断下行剖腹探查术。在距盲肠口120cm处的回肠末端观察到缺血性改变。该部位被切除。在整个肠腔内发现多个线性和口疮样溃疡病变。组织病理学检查显示,在溃疡病变下方黏膜下层的小动脉中有坏死性血管炎的证据,如纤维蛋白样坏死和壁血栓形成。病例2:一名63岁女性,自1980年起患有RA,1989年7月出现恶心、腹痛和血性腹泻。结肠镜检查显示乙状结肠有多个线性和口疮样溃疡,推测是由缺血引起。当时的实验室检查显示补体血症、循环免疫复合物阳性和抗DNA抗体高滴度。中等剂量的皮质类固醇治疗成功缓解了所有异常表现,患者在首次胃肠道发作三个月后完全康复。