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表现为风湿性多肌痛-颞动脉炎综合征的颞动脉非巨细胞动脉炎

Non-giant cell arteritis of the temporal artery presenting as the polymyalgia rheumatica-temporal arteritis syndrome.

作者信息

Lesser R S, Aledort D, Lie J T

机构信息

Brookdale Hospital Medical Center, Brooklyn, NY, Rheumatology Section 11212-3198, USA.

出版信息

J Rheumatol. 1995 Nov;22(11):2177-82.

PMID:8596167
Abstract

We describe a heterogeneous group of 4 elderly patients with atypical vasculitis of the temporal artery who presented clinically with the polymyalgia rheumatica-temporal arteritis syndrome. The first had apparently isolated eosinophilic necrotizing vasculitis without peripheral blood eosinophilia, history of asthma, or pulmonary vasculitis (so called limited form of Churg-Strauss syndrome). Temporal artery biopsy in the 2nd patient revealed small vessel necrotizing vasculitis in the fragment of skeletal muscle surrounding a normal temporal artery (i.e., negative for giant cell arteritis, GCA). This patient subsequently developed rheumatoid polysynovitis. The temporal artery biopsies in the remaining 2 patients showed vasa vasorum vasculitis, without GCA, associated with malignancy in Patient 3 and as an unexpected and apparently isolated finding in Patient 4. All 4 patients responded to the standard corticosteroid therapy for giant cell temporal arteritis. Unusual temporal artery biopsies such as these should be interpreted in relation to clinical findings.

摘要

我们描述了一组异质性的4例老年颞动脉非典型血管炎患者,这些患者临床上表现为风湿性多肌痛-颞动脉炎综合征。第一例患者显然为孤立性嗜酸性坏死性血管炎,无外周血嗜酸性粒细胞增多、哮喘病史或肺血管炎(即所谓的局限性变应性肉芽肿性血管炎)。第二例患者的颞动脉活检显示,在正常颞动脉周围的骨骼肌碎片中有小血管坏死性血管炎(即巨细胞动脉炎,GCA阴性)。该患者随后发展为类风湿性多滑膜炎。其余2例患者的颞动脉活检显示血管滋养管血管炎,无GCA,第3例患者与恶性肿瘤相关,第4例患者为意外的、显然孤立的发现。所有4例患者对巨细胞颞动脉炎的标准皮质类固醇治疗均有反应。此类不寻常的颞动脉活检结果应结合临床发现进行解读。

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