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系统性硬皮病患者低剂量口服皮质类固醇和米佐米滨联合治疗溃疡性结肠炎。

Combinational effect of low-dose oral corticosteroid and mizoribine for ulcerative colitis in a patient with systemic sclerosis.

机构信息

Department of Dermatology, Koshigaya Hospital, Dokkyo Medical University, Saitama 343-8555, Japan.

出版信息

J Dermatol. 2010 Jan;37(1):71-4. doi: 10.1111/j.1346-8138.2009.00749.x.

Abstract

The combinational effect of oral corticosteroid and mizoribine for ulcerative colitis is presented in a patient with systemic sclerosis (SSc). A 64-year-old woman came to our clinic complaining of a 30-year history of Raynaud's phenomenon. She had past history of ulcerative colitis with the continued medication of mesalazine without success. She was presented with sclerodactyly and finger joint swelling. She also showed epigastric discomfort. Laboratory study showed positive anti-nuclear antibody and positive anti-centromere antibody. Histological examination showed mild perivascular mononuclear cell infiltrates in the whole dermis and increased deposition of collagen fibers in the middle and lower dermis. Chest X-ray film showed mild bibasilar pulmonary fibrosis. An upper gastrointestinal series study showed reflux esophagitis and atrophic gastritis. These findings led to the diagnosis of systemic sclerosis (limited type) complicated with ulcerative colitis. Treatment with oral corticosteroid (5 mg/day) and mizoribine (150 mg/day) in the morning was started. She showed remarkable improvement for sclerodactyly and lower intestinal bleeding stopped after 6 months. She is under the same treatment without exaggeration and adverse effect of the drug until now.

摘要

一位系统性硬化症(SSc)合并溃疡性结肠炎患者接受了口服皮质类固醇和米佐米滨联合治疗。一位 64 岁女性因雷诺现象 30 年就诊于我院。她既往有溃疡性结肠炎病史,曾服用美沙拉嗪但效果不佳。现出现硬皮病和指关节肿胀,同时伴有上腹部不适。实验室检查抗核抗体和抗着丝点抗体阳性。组织学检查显示整个真皮层轻度血管周围单核细胞浸润,真皮中、下层胶原纤维沉积增加。胸部 X 线片显示轻度双基底肺纤维化。上消化道系列研究显示反流性食管炎和萎缩性胃炎。这些发现提示诊断为系统性硬化症(局限型)合并溃疡性结肠炎。开始给予口服皮质类固醇(5mg/天)和米佐米滨(150mg/天)治疗。治疗 6 个月后,患者硬皮病明显改善,下消化道出血停止。目前,她仍在接受相同的治疗,无药物加重或不良反应。

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