Suppr超能文献

以胸痛为表现的肉芽肿性多血管炎:一例报告

Granulomatosis With Polyangiitis Presenting as Chest Pain: A Case Report.

作者信息

Fentie Kindalem, Singanamala Swathi, Hozayen Omar, Altaf Lareb

机构信息

Medicine, Trinity Medical Sciences University, Warner Robins, USA.

Nephrology, Piedmont HealthCare, Macon, USA.

出版信息

Cureus. 2023 Apr 27;15(4):e38204. doi: 10.7759/cureus.38204. eCollection 2023 Apr.

Abstract

Granulomatosis with polyangiitis (GPA) is a relatively rare systemic autoimmune disorder of small and medium size blood vessels affecting multiple organs with a wide range of clinical presentations. We present a 57-year-old Caucasian male who presented to the ER with midsternal chest pain. He was hospitalized for non-ST elevated myocardial infarction (NSTEMI) and later diagnosed with pauci-immune necrotizing crescentic glomerulonephritis confirmed with renal biopsy.

摘要

肉芽肿性多血管炎(GPA)是一种相对罕见的累及中小血管的系统性自身免疫性疾病,可影响多个器官,临床表现多样。我们报告一名57岁的白种男性,因胸骨后胸痛就诊于急诊室。他因非ST段抬高型心肌梗死(NSTEMI)住院,后来经肾活检确诊为寡免疫坏死性新月体性肾小球肾炎。

相似文献

8
Granulomatosis with polyangiitis associated with IgA nephropathy.肉芽肿性多血管炎合并IgA肾病
CEN Case Rep. 2013 Nov;2(2):204-208. doi: 10.1007/s13730-013-0065-2. Epub 2013 Feb 20.

本文引用的文献

4
ANCA-associated vasculitis.抗中性粒细胞胞浆抗体相关性血管炎
Clin Med (Lond). 2017 Feb;17(1):60-64. doi: 10.7861/clinmedicine.17-1-60.
6
Cardiac Involvement in Granulomatosis with Polyangiitis.肉芽肿性多血管炎的心脏受累情况
J Rheumatol. 2015 Jul;42(7):1209-12. doi: 10.3899/jrheum.141513. Epub 2015 May 1.

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