肉芽肿伴多血管炎——不完全之谜。

IF 1 4区 医学 Q4 RHEUMATOLOGY
Acta reumatologica portuguesa Pub Date : 2021-10-01
Ana Catarina Duarte, Ana Cordeiro, Pedro Gonçalves, Maria José Santos
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引用次数: 0

摘要

肉芽肿性多血管炎(GPA)是一种坏死性肉芽肿性血管炎,主要影响小血管。该病可累及许多器官,但累及肾脏和呼吸道是最常见和最显著的特征。约50%的患者有肌肉骨骼表现,可表现为肌痛、大关节少关节痛/关节炎或小关节多关节痛/关节炎。在罕见的情况下,肌肉骨骼症状可能是疾病的第一表现,在这种临床情况下,GPA诊断可能被其他风湿病延迟或错误。作者描述了三例以肌肉骨骼症状为早期GPA表现的患者,说明了临床挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Granulomatosis with polyangiitis - the incomplete puzzle.

Granulomatous with polyangiitis (GPA) is a necrotizing granulomatous vasculitis that mostly affects small-sized vessels. The disease can affect many organs, although renal and respiratory tract involvement are the most frequent and distinguishing features. Musculoskeletal manifestations have been reported in about 50% of patients and can occur as myalgia, oligoarthralgia/arthritis of large joints or polyarthralgia/arthritis of small joints. Infrequently musculoskeletal symptoms can be the first disease manifestation, and in this clinical scenario GPA diagnosis might be delayed or mistaken by other rheumatic diseases. The authors describe three patients with musculoskeletal symptoms as earliest GPA manifestations, illustrating the clinical challenge.

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来源期刊
Acta reumatologica portuguesa
Acta reumatologica portuguesa 医学-风湿病学
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Acta Reumatólogica Portuguesa is a scientific peer reviewed journal covering all aspects of rheumatic diseases and related to Rheumatology. The journal publishes original articles, reviews, clinical cases, images in rheumatology, letters to the editor and clinical teaching (e.g. guidelines and clinical protocols). Published since 1973, Acta Reumatológica Portuguesa is the official scientific publication of the Portuguese Society of Rheumatology, a non-profit organization that promotes the knowledge and investigation of rheumatic diseases and the development of Rheumatology.
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