Rapid and sustained remission of synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome with IL-23p19 antagonist (risankizumab)
Akshay Flora, Richard Holland, Annika Smith, John W. Frew
Abstract
Akshay Flora, Richard Holland, Annika Smith, John W. Frew
Abstract
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is an uncommon autoinflammatory syndrome, with an estimated prevalence of 1 in 10,000 in the Caucasian population.1 SAPHO is defined by the diagnostic criteria proposed by Kahn et al,2 which includes either a chronic multifocal sterile osteomyelitis, sterile osteitis, or arthritis.1,3 The latter 2 require at least 1 accompanying dermatologic feature, which includes palmoplantar pustulosis, pustular psoriasis, or severe acne.
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Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is an uncommon autoinflammatory syndrome, with an estimated prevalence of 1 in 10,000 in the Caucasian population.1 SAPHO is defined by the diagnostic criteria proposed by Kahn et al,2 which includes either a chronic multifocal sterile osteomyelitis, sterile osteitis, or arthritis.1,3 The latter 2 require at least 1 accompanying dermatologic feature, which includes palmoplantar pustulosis, pustular psoriasis, or severe acne.
Key concepts: SAPHO syndrome, Palmoplantar pustulosis, Pustulosis, Medicine, Hyperostosis, Osteitis, Synovitis, Dermatology