Current Rheumatology Reports ( IF 5.7 ) Pub Date : 2022-09-21 , DOI: 10.1007/s11926-022-01088-0 Kinanah Yaseen 1 , Alana Nevares 2 , Hiromichi Tamaki 3
Purpose of Review
Drug-induced vasculitis (DIV) is a rare form of vasculitis related to the use of various drugs. DIV primarily affects small to medium size vessels, but it can potentially involve vessels of any size. Differentiating between primary systemic vasculitis and DIV can be challenging; however, it is crucial, so that the offending agent can be discontinued promptly.
Recent Findings
The clinical phenotype of DIV is protean and depends on the size of the affected vessels. It ranges from arthralgias, to an isolated cutaneous rash, to severe single or multi-organ involvement. While withdrawal of the offending drug is the most important step in management, a significant number of patients require immunosuppressive therapy for varying periods of time.
Summary
DIV can affect any vascular bed size, leading to protean vasculitic syndromes. Increased awareness among general practitioners, specialty, and subspecialty physicians is crucial for early recognition, and withdrawal of drug for better outcomes.
中文翻译:
聚焦药物性血管炎
审查目的
药物性血管炎 (DIV) 是一种罕见的血管炎,与使用各种药物有关。DIV 主要影响中小型血管,但它可能涉及任何大小的血管。区分原发性系统性血管炎和 DIV 可能具有挑战性;然而,这很重要,这样可以立即停用违规药物。
最近的发现
DIV 的临床表型千变万化,取决于受影响血管的大小。它的范围从关节痛到孤立的皮疹,再到严重的单器官或多器官受累。虽然停用致病药物是管理中最重要的步骤,但仍有大量患者需要在不同时期接受免疫抑制治疗。
概括
DIV 可影响任何血管床大小,导致千变万化的血管炎综合征。提高全科医生、专科和亚专科医师的意识对于早期识别和停药以获得更好的结果至关重要。