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本文引用的文献

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First international consensus on the diagnosis and management of fibromuscular dysplasia.纤维肌性发育不良的诊断与管理:国际首项共识
J Hypertens. 2019 Feb;37(2):229-252. doi: 10.1097/HJH.0000000000002019.
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Clinical phenotypes of IgG4-related disease: an analysis of two international cross-sectional cohorts.IgG4 相关疾病的临床表型:两项国际横断面队列研究的分析。
Ann Rheum Dis. 2019 Mar;78(3):406-412. doi: 10.1136/annrheumdis-2018-214603. Epub 2019 Jan 5.
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Arterial involvement in Erdheim-Chester disease: A retrospective cohort study.厄德里希-切斯特病的动脉受累情况:一项回顾性队列研究。
Medicine (Baltimore). 2018 Dec;97(49):e13452. doi: 10.1097/MD.0000000000013452.
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Polyarteritis nodosa: lessons from 25 years of experience.结节性多动脉炎:25 年经验教训。
Clin Exp Rheumatol. 2019 Mar-Apr;37 Suppl 117(2):52-56. Epub 2018 Oct 30.
5
Urticaria: A comprehensive review: Epidemiology, diagnosis, and work-up.荨麻疹:全面综述:流行病学、诊断和检查。
J Am Acad Dermatol. 2018 Oct;79(4):599-614. doi: 10.1016/j.jaad.2018.01.020.
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2018 update of the EULAR recommendations for the management of Behçet's syndrome.2018 年更新的欧洲抗风湿病联盟白塞病治疗推荐。
Ann Rheum Dis. 2018 Jun;77(6):808-818. doi: 10.1136/annrheumdis-2018-213225. Epub 2018 Apr 6.
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Pyoderma gangrenosum: a review of pathogenesis and treatment.坏疽性脓皮病:发病机制与治疗的综述。
Expert Rev Clin Immunol. 2018 Mar;14(3):225-233. doi: 10.1080/1744666X.2018.1438269. Epub 2018 Feb 13.
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Current treatment of central retinal artery occlusion: a national survey.目前对视网膜中央动脉阻塞的治疗:一项全国性调查。
J Neurol. 2018 Feb;265(2):330-335. doi: 10.1007/s00415-017-8702-x. Epub 2017 Dec 13.
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Relapsing polychondritis: a clinical review for rheumatologists.复发性多软骨炎:风湿科医生的临床综述。
Rheumatology (Oxford). 2018 Sep 1;57(9):1525-1532. doi: 10.1093/rheumatology/kex406.
10
Evaluation and Management of Lower-Extremity Ulcers.下肢溃疡的评估与管理
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基于 Chapel Hill 共识分类的原发性血管炎模仿者综述

A Review of Primary Vasculitis Mimickers Based on the Chapel Hill Consensus Classification.

作者信息

Zarka Farah, Veillette Charles, Makhzoum Jean-Paul

机构信息

Hôpital du Sacré-Cœur de Montreal, University of Montreal, Canada.

Vasculitis Clinic, Department of Internal Medicine, Hôpital du Sacré-Coeur de Montreal, University of Montreal, Canada.

出版信息

Int J Rheumatol. 2020 Feb 18;2020:8392542. doi: 10.1155/2020/8392542. eCollection 2020.

DOI:10.1155/2020/8392542
PMID:32148510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7049422/
Abstract

Primary systemic vasculitides are rare diseases that may manifest similarly to more commonly encountered conditions. Depending on the size of the vessel affected (large vessel, medium vessel, or small vessel), different vasculitis mimics must be considered. Establishing the right diagnosis of a vasculitis mimic will prevent unnecessary immunosuppressive therapy.

摘要

原发性系统性血管炎是罕见疾病,其表现可能与更常见的病症相似。根据受累血管的大小(大血管、中血管或小血管),必须考虑不同的血管炎模仿病症。正确诊断血管炎模仿病症可避免不必要的免疫抑制治疗。