Tanaz A Kermani,Kenneth J Warrington
Tanaz A Kermani
Giant cell arteritis is a large-vessel vasculitis affecting the aorta and its branches. While treatment with glucocorticoids is efficacious in the initial management, patients experience relapses and adverse effects.
Avacopan may not independently reduce ANCA titres in ANCA-Associated vasculitis: a retrospective analysis of 57 patients [0.03%]
阿瓦普利单抗不能独立降低肉芽肿性多血管炎患者ANCA滴度：57例患者的回顾性分析
Motoki Takeuchi,Yoshiyuki Abe,Masahiro Kogami et al.
Motoki Takeuchi et al.
Clinicodemographic Data of Patients with Behçet's Disease: Data from a Tertiary Center in Saudi Arabia [0.03%]
沙特阿拉伯三级医疗中心Behçet病患者的门诊人口统计资料
Yasser Bawazir,Mohammad Mustafa
Yasser Bawazir
Introduction: Behçet's disease (BD) is a chronic inflammatory vasculitis involving the arteries and veins. This study was driven by the rarity, chronic multisystemic nature, and heterogeneous spectrum of clinical features and geographical distribution.
A male patient with proptosis and palatal perforation: A diagnostic challenge [0.03%]
一位眼睑下垂伴咽瘘的男性患者：一项重大的诊断挑战
Peyman Mottaghi,Sam Mirfendereski,Farshad Riahi et al.
Peyman Mottaghi et al.
Rare complications of this vasculitis syndrome include a retroorbital pseudotumor with proptosis due to chronic tissue inflammation, as well as necrosis with subsequent palate perforation.
Unveiling the gut-heart potential connection: microbiota's role in kawasaki disease and coronary artery lesions [0.03%]
揭秘肠道-心脏潜在连接：微生物群在川崎病和冠状动脉病变中的作用
Qing Yang,Wei Tang,Jiayu Ren et al.
Qing Yang et al.
Background: Kawasaki disease (KD) is an acute systemic immune vasculitis predominantly affecting medium and small arteries, commonly observed in pediatric patients. It represents the most common form of acquired heart disease in this population.
Neutrophil Extracellular Traps in Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis: Diagnostic and Clinical Significance-A Review of the Current Literature [0.03%]
抗中性粒细胞胞浆抗体相关性血管炎中中性粒细胞胞外陷阱的诊断及临床意义：文献综述
Sylwester Drożdżal,Aleksandra Gomółka,Martyna Opara-Bajerowicz et al.
Sylwester Drożdżal et al.
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of rare but potentially life-threatening autoimmune diseases that affect small to medium-sized blood vessels.
A randomized, double-blind, placebo-controlled trial of abatacept for the treatment of relapsing, non-severe, granulomatosis with polyangiitis [0.03%]
阿巴西普治疗复发性非重症肉芽肿性多血管炎的随机双盲安慰剂对照试验
Carol A Langford,Nader Khalidi,Jason Springer et al.
Carol A Langford et al.
Objective: To compare the efficacy of abatacept to placebo for the treatment of relapsing, non-severe granulomatosis with polyangiitis (GPA). Methods: ...
Kornelis S M van der Geest,Berend G C Slijkhuis,Alessandro Tomelleri et al.
Kornelis S M van der Geest et al.
Systemic vasculitides comprise a group of autoimmune diseases affecting blood vessels. [18F]-fluoro-2-deoxy-d-glucose positron emission tomography/computed tomography (FDG-PET/CT) plays an important role in the diagnosis and therapeutic mon...
ANCA-associated vasculitis in a middle-aged woman with HIV: a complex interplay and therapeutic challenges [0.03%]
人类免疫缺陷病毒感染中年女性的抗中性粒细胞胞浆抗体血管炎：复杂的相互作用和治疗挑战
Sreejith Prathapa Chandran Vanajakumari,Parikshit Chauhan,Atul Kumar Srivastava et al.
Sreejith Prathapa Chandran Vanajakumari et al.
Despite this variability, clinically significant ANCA-associated vasculitis (AAV) remains rare. We report the case of a woman in her 40s with stable HIV infection who developed systemic microscopic polyangiitis with severe renal impairment.
Case Reports
BMJ case reports. 2025 Jun 12;18(6):e262359. DOI:10.1136/bcr-2024-262359 2025
Benjamin Y Hsieh,Mohamed Ismail,Menna-Allah Elaskandrany
Benjamin Y Hsieh
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