坏疽性脓皮病
托法替尼
医学
贾纳斯激酶
皮肤病科
中性粒细胞性皮肤病
相伴的
活检
内科学
细胞因子
疾病
类风湿性关节炎
作者
Vanitha Agrahara Sathyanarayana,Debaditya Roy,Bhavya Nagaraju,Vijay Rao
标识
DOI:10.1111/1756-185x.14810
摘要
Abstract Pyoderma gangrenosum (PG) is a rare autoinflammatory disorder falling under the spectrum of neutrophilic dermatosis, characterized by distinctive skin ulceration which is non‐infective, non‐neoplastic and usually with no primary vasculitis. PG lesions are notorious for relapse and hence require multiple trials of medications often with prolonged and concomitant use of steroids. Due to lack of evidence‐based studies on effective treatment options for PG, we have presented three isolated biopsy‐proven PG cases who were successfully treated with Tofacitinib, a Janus kinase/signal transducers and activators of transcription (JAK/STAT) pathway inhibitor, without relapse in follow up.
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