坏疽性脓皮病
医学
美罗华
肉芽肿伴多发性血管炎
耐火材料(行星科学)
免疫抑制
显微镜下多血管炎
血管炎
皮肤病科
中性粒细胞性皮肤病
外科
病理
内科学
淋巴瘤
疾病
物理
天体生物学
作者
Vanessa Tran,S. Chatfield,Armando Torres,Laura Scardamaglia
出处
期刊:Case Reports
[BMJ]
日期:2025-01-01
卷期号:18 (1): e262584-e262584
标识
DOI:10.1136/bcr-2024-262584
摘要
Granulomatosis with polyangiitis (GPA) is a small-to-medium vessel vasculitis that can affect the skin, respiratory tract, kidneys and other organs. A rare cutaneous manifestation of GPA is pyoderma gangrenosum (PG)-like ulcerations, which can have debilitating and disfiguring consequences. We report the case of a man in his 40s with refractory PG-like ulcerations secondary to GPA, not responsive to conventional immunosuppression, who was successfully treated with rituximab. This case emphasises the need for early recognition of this rare manifestation to allow for prompt initiation of treatment.
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