Suppr超能文献

[1例复发为消化道出血且治疗困难的MPO-ANCA相关性血管炎]

[A case of MPO-ANCA-related vasculitis that recurred as gastrointestinal bleeding and presented difficulty in treatment].

作者信息

Inaguma D, Kurata K, Ishihara S, Machida H, Yaomura T, Kumon S

机构信息

Department of Nephrology, Tosei General Hospital, Aichi, Japan.

出版信息

Nihon Jinzo Gakkai Shi. 1998 Sep;40(7):560-5.

PMID:9805923
Abstract

A 54-year-old man, who had been diagnosed as having MPO-ANCA-related glomerulonephritis in 1993, developed severe anemia and was admitted to our hospital on October, 1997. Endoscopic examination of the upper gastrointestinal tract revealed melena due to duodenal ulcer (Dieulafoy type). The level of ANCA titer was elevated considerably (640 EU), but otherwise there was no evidence of systemic vasculitis activation such as fever, arthralgia, skin eruption, renal insufficiency, and rise in C reactive protein. A renal biopsy showed neither crescentic formation nor necrosis of glomerulus. Subsequently he developed hematochezia and renal dysfunction rapidly progressed thereafter. Angiographical examination of superior mesenteric artery revealed that the bleeding was responsible for the lesion of the small intestine, probably the ileum. In spite of TAE (transarterial embolization) he had recurrence of severe hematochezia three days later. Partial ileotomy was performed and progression of the anemia was stopped. Multiple ulcer was found in the resected ileum. The small arteries in the submucosa at the ulceration showed fibrinoid necrosis of the vessel walls. These findings suggested that ANCA-related vasculitis had relapsed. The patient received methylprednisolone pulse therapy, followed by oral administration of prednisolone after the operation. Both serum levels of creatinine and MPO-ANCA gradually decreased after the initiation of treatment. However, 24 days later, he suddenly manifested severe abdominal pain, and was diagnosed as having perforation of the stomach or duodenum. Due to supportive therapy and reduction of the steroid dose, peritonitis subsided, but symptoms caused by systemic vasculitis developed. Later raised the dose of steroid suppressed the activity of systemic vasculitis. In this case, elevation of the ANCA titer demonstrated recurrence of MPO-ANCA-related vasculitis as gastrointestinal bleeding.

摘要

一名54岁男性,1993年被诊断为患有MPO - ANCA相关性肾小球肾炎,1997年10月出现严重贫血并入住我院。上消化道内镜检查发现十二指肠溃疡(Dieulafoy型)导致的黑便。ANCA滴度显著升高(640 EU),但除此之外,没有发热、关节痛、皮疹、肾功能不全和C反应蛋白升高等系统性血管炎激活的证据。肾活检未发现肾小球新月体形成或坏死。随后他出现便血,此后肾功能迅速恶化。肠系膜上动脉血管造影检查显示出血是由小肠(可能是回肠)病变引起的。尽管进行了经动脉栓塞术(TAE),但三天后他再次出现严重便血。进行了部分回肠切除术,贫血进展得以停止。在切除的回肠中发现多个溃疡。溃疡处黏膜下层的小动脉显示血管壁纤维蛋白样坏死。这些发现提示ANCA相关性血管炎复发。患者接受了甲泼尼龙冲击治疗,术后口服泼尼松龙。治疗开始后,血清肌酐水平和MPO - ANCA均逐渐下降。然而,24天后,他突然出现严重腹痛,被诊断为胃或十二指肠穿孔。由于支持治疗和类固醇剂量的减少,腹膜炎消退,但出现了系统性血管炎引起的症状。后来增加类固醇剂量抑制了系统性血管炎的活动。在本病例中,ANCA滴度升高表明MPO - ANCA相关性血管炎复发表现为胃肠道出血。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验