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阿达木单抗成功治疗坏疽性脓皮病、斑块状银屑病和掌跖脓疱病患者
Authors Chu Y, Liu T, Bai J, Fang H, Qiao J
Received 6 May 2022
Accepted for publication 26 July 2022
Published 20 September 2022 Volume 2022:15 Pages 1991—1995
DOI https://doi.org/10.2147/CCID.S373115
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Dr Jeffrey Weinberg
Abstract: Pyoderma gangrenosum (PG) is a rare autoinflammatory skin disorder, which is characterised by rapidly developing and tender cutaneous ulcers. The treatment of PG is challenging. Palmoplantar pustulosis (PPP) is also an autoinflammatory dermatosis with sterile pustules on the palms and/or the soles. We demonstrated a 68-year-old patient with coexisting autoinflammatory diseases including PG, 1-year history of plaque psoriasis and PPP, recovered after treatment with adalimumab. We also reviewed published reports of PG-associated autoinflammatory syndromes with adalimumab.
Keywords: adalimumab, autoinflammatory syndrome, palmoplantar pustulosis, plaque psoriasis, pyoderma gangrenosum