一种与扩散性膜出血相关的多性炎的eosinophilic granulomatosis病例:一个病例报告和基于病例的审查
Rira Kawaguchi1, Hirohisa Usagawa1, Yoshia Miyawaki2
1Department of Rheumatology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.
Modern rheumatology case reports
|April 27, 2024
概括
带有多胞膜炎 (EGPA) 的埃索诺菲尔颗粒瘤可能导致扩散性膜出血 (AH),这是一个罕见但危及生命的并发症. 关键指标包括男性占主导地位,阳性髓氧化酶-抗核细胞质抗体 (MPO-ANCA) 和频繁的脏干扰.
科学领域:
- 医学 医学 医学 医学 医学
- 肺部病理学 肺部病理学
- 类风湿病学 类风湿病学
背景情况:
- 扩散膜出血 (AH) 是一种罕见但严重的并发症.
- 带有多炎 (EGPA) 的异性粒状炎是一种系统性血管炎,其特点是喘,异性和多系统参与.
研究的目的:
- 介绍一例与EGPA相关的AH.
- 审查EGPA中关于AH的文献,并确定其特征特征.
主要方法:
- 一个76岁的老人患有呼吸衰竭和血的病例报告.
- 关于AH的EGPA病例的文献综述.
主要成果:
- 该患者被诊断为EGPA相关的AH,由阳性MPO-ANCA证实,并证实了淋巴细胞炎.
- 文献审查表明,在EGPA相关的AH中,男性占主导地位 (65%),高ANCA阳性 (88%) 和频繁的脏参与 (45%).
结论:
- 这是一种罕见但关键的EGPA表现,需要及时识别.
- 临床和实验室发现,如MPO-ANCA阳性和脏参与,对于诊断EGPA患者的AH很重要.
关键词:
带有多炎的埃索诺菲尔颗粒症.鼓膜出血 鼓膜出血 鼓膜出血球体突性耳炎 (glomeruronephritis) 是一个严重的疾病.血清细胞结合性血管炎 (leukocytoclastic vasculitis) 是一种致血性血管炎.更多相关视频
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