首页> 美国卫生研究院文献>Internal Medicine >Encapsulating Peritoneal Sclerosis in Systemic Lupus Erythematosus Rheumatoid Arthritis and Systemic Sclerosis
【2h】

Encapsulating Peritoneal Sclerosis in Systemic Lupus Erythematosus Rheumatoid Arthritis and Systemic Sclerosis

机译:系统性红斑狼疮、类风湿性关节炎和系统性硬化症的包膜腹膜硬化症

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We encountered a 57-year-old Japanese woman with encapsulating peritoneal sclerosis (EPS) in systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), and systemic sclerosis. The patient was admitted to our hospital because of ascites retention. Administration of tocilizumab, an anti-interleukin-6 receptor antibody, for her RA reduced the refractory ascites remarkably; however, she developed sudden acute gastrointestinal bleeding and died a year later. On autopsy, sclerotic thickening of the peritoneum showed diffuse infiltration of podoplanin-positive fibroblast-like cells, and a diagnosis of EPS was made. EPS rarely occurs in SLE, and tocilizumab may be a new treatment candidate for EPS.
机译:我们遇到了一名 57 岁的日本女性,她患有系统性红斑狼疮 (SLE)、类风湿性关节炎 (RA) 和系统性硬化症中的包膜性腹膜硬化症 (EPS)。患者因腹水潴留入住我院。托珠单抗(一种抗白细胞介素 6 受体抗体)治疗她的 RA 显着减少了难治性腹水;然而,她突然出现急性胃肠道出血,一年后去世。尸检发现腹膜硬化增厚显示 podoplanin 阳性成纤维细胞样细胞弥漫性浸润,诊断为 EPS。EPS 很少发生在 SLE 中,托珠单抗可能是 EPS 的新治疗候选者。

著录项

代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号