{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["16"],"submitter":["Yang Y"],"pubmed_abstract":["Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome, a rare autoinflammatory disease, is usually defined by musculoskeletal symptoms and cutaneous manifestations. Cutaneous manifestations include palmoplantar pustulosis or severe acne, which are generally accompanied by osteitis and hyperostosis, and are the hallmark of SAPHO syndrome. Genetic, immune, and microbial factors are involved in the pathophysiology of the SAPHO. Small-molecule targeted therapies and biologic agents have transformed the treatment of inflammatory disorders. Upadacitinib, with efficacy in cytokine-related disorders, represents a therapeutic candidate for SAPHO syndrome. Here we report a patient with a 20-year history of pustular palmoplantar psoriasis (PPP) who developed progressive inflammator"],"journal":["Frontiers in immunology"],"pagination":["1662675"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12669195"],"repository":["biostudies-literature"],"pubmed_title":["Upadacitinib in the treatment of SAPHO syndrome: a case report."],"pmcid":["PMC12669195"],"pubmed_authors":["Yang Y","Ge Y","Sun Z"],"additional_accession":[]},"is_claimable":false,"name":"Upadacitinib in the treatment of SAPHO syndrome: a case report.","description":"Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome, a rare autoinflammatory disease, is usually defined by musculoskeletal symptoms and cutaneous manifestations. Cutaneous manifestations include palmoplantar pustulosis or severe acne, which are generally accompanied by osteitis and hyperostosis, and are the hallmark of SAPHO syndrome. Genetic, immune, and microbial factors are involved in the pathophysiology of the SAPHO. Small-molecule targeted therapies and biologic agents have transformed the treatment of inflammatory disorders. Upadacitinib, with efficacy in cytokine-related disorders, represents a therapeutic candidate for SAPHO syndrome. Here we report a patient with a 20-year history of pustular palmoplantar psoriasis (PPP) who developed progressive inflammator","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025","modification":"2026-06-08T04:52:55.971Z","creation":"2026-06-08T03:08:49.913Z"},"accession":"S-EPMC12669195","cross_references":{"pubmed":["41341579"],"doi":["10.3389/fimmu.2025.1662675"]}}