医学
美罗华
氨苯砜
回顾性队列研究
皮肤病科
耐火材料(行星科学)
血管炎
免疫学
内科学
疾病
外科
淋巴瘤
天体生物学
物理
作者
Thomas Bettuzzi,A. Deroux,M. Jachiet,Meryem‐Maud Farhat,J. Wipff,Marc Fabre,Laurence Bouillet,N. Kramkimel,S. Aractingi,N. Dupin,Benjamin Terrier
标识
DOI:10.1136/annrheumdis-2019-215605
摘要
Urticarial vasculitis (UV) is rare systemic disease characterised by a dermal capillary inflammation responsible of long-lasting urticarial lesions, and sometimes some systemic manifestations.1 2 UV can be separated into two different entities: hypocomplementemic UV (HUV) and normocomplementemic UV (NUV). Treatment of UV depends on the severity of the disease and the occurrence of relapses. In patients refractory to colchicine or dapsone, glucocorticoids (GCs), conventional immunosuppressive agents or rituximab (RTX) can be used,1 2 leading to significant morbidity. Interleukin-1β (IL-1β) inhibitors are biologics mainly used in autoinflammatory diseases.3 We report here a French retrospective multicentr study of patients treated with IL-1β inhibitors for persistent disease despite GCs and/or immunosuppressive agents.
This French retrospective multicentre study was conducted in four departments of Dermatology and Internal Medicine. We included patients with persistent UV to at …
科研通智能强力驱动
Strongly Powered by AbleSci AI