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使用苏金单抗成功治疗难治性滑膜炎、痤疮、脓疱病、骨质增生和骨炎 (SAPHO) 综合征和矛盾型银屑病:病例报告
Authors Fan D, Li F , Liu Z, Tang Z, Lv S
Received 8 December 2023
Accepted for publication 21 February 2024
Published 5 March 2024 Volume 2024:17 Pages 547—552
DOI https://doi.org/10.2147/CCID.S454057
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Jeffrey Weinberg
Abstract: Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a rare chronic inflammatory disease mainly manifested as skin and osteoarticular lesions. Herein, we describe a female patient with SAPHO syndrome exhibited paradoxical psoriasis and primary palmoplantar pustulosis (PPP) worsened during treatment with adalimumab. We then switched to secukinumab and obtained significant improvement in both skin lesions and osteoarticular pain. These findings suggest that secukinumab might be an appropriate option for patients with SAPHO syndrome who present with TNF-α-inhibitor-induced paradoxical psoriasis.
Keywords: SAPHO syndrome, psoriasis, adalimumab, secukinumab