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巨细胞(肌)动脉炎和其他中、大血管血管炎。

Medium- and Large-Vessel Vasculitis.

机构信息

Sorbonne Universités, Assistance Publique Hôpitaux de Paris (AP-HP), Pitié-Salpêtrière University Hospital, Department of Internal Medicine and Clinical Immunology, Centre national de Référence des Maladies Auto-Immunes Systémiques Rares, Centre national de Référence des Maladies Auto-Inflammatoires et de l'Amylose inflammatoire, Paris, France (D.S., M.V.).

Institut National de la Santé et de la Recherche Médicale (INSERM), Unité mixte de recherche (UMR) S 959, and Recherche Hospitalo-Universitaire en santé (RHU) Interleukin-2 Therapy for autoimmune and inflammatory diseases, Paris, France (D.S., P.C.).

出版信息

Circulation. 2021 Jan 19;143(3):267-282. doi: 10.1161/CIRCULATIONAHA.120.046657.

Abstract

Systemic vasculitides are multisystem blood vessel disorders, which are defined by the size of the vessel predominantly affected, namely small, medium, or large vessels. The term "large vessel" relates to the aorta and its major branches; "medium vessel" refers to the main visceral arteries and veins and their initial branches. The most common causes of large-vessel vasculitis are giant cell arteritis and Takayasu arteritis, and those of medium-vessel arteritis are polyarteritis nodosa and Kawasaki disease. However, there is some overlap, and arteries of any size can potentially be involved in any of the 3 main categories of dominant vessel involvement. In addition to multisystem vasculitides, other forms of vasculitis have been defined, including single-organ vasculitis (eg, isolated aortitis). Prompt identification of vasculitides is important because they are associated with an increased risk of mortality. Left undiagnosed or mismanaged, these conditions may result in serious adverse outcomes that might otherwise have been avoided or minimized. The ethnic and regional differences in the incidence, prevalence, and clinical characteristics of patients with vasculitis should be recognized. Because the clinical presentation of vasculitis is highly variable, the cardiovascular clinician must have a high index of suspicion to establish a reliable and prompt diagnosis. This article reviews the pathophysiology, epidemiology, diagnostic strategies, and management of vasculitis.

摘要

系统性血管炎是一种多系统血管疾病,根据主要受累血管的大小来定义,主要包括小血管、中血管或大血管。“大血管”术语涉及主动脉及其主要分支;“中血管”指的是主要内脏动脉和静脉及其初始分支。大血管血管炎最常见的病因是巨细胞性动脉炎和 Takayasu 动脉炎,中血管血管炎的病因是结节性多动脉炎和川崎病。然而,这些病因之间存在一些重叠,任何大小的动脉都可能涉及到 3 种主要的主要血管受累类别中的任何一种。除了多系统血管炎,还定义了其他形式的血管炎,包括单器官血管炎(例如孤立性主动脉炎)。及时识别血管炎很重要,因为它们与死亡率增加有关。如果未被诊断或管理不当,这些疾病可能会导致严重的不良后果,否则这些后果是可以避免或最小化的。应该认识到血管炎患者的发病率、患病率和临床特征在种族和地区之间存在差异。由于血管炎的临床表现高度多样化,心血管临床医生必须高度怀疑,以建立可靠和及时的诊断。本文综述了血管炎的病理生理学、流行病学、诊断策略和治疗。

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