Family aggregation and prevalence of other autoimmune diseases in SAPHO syndrome [PDF]
Objective: SAPHO (Synovitis, Acne, Pustulosis, Hyperostosis and Osteitis) syndrome is a heterogeneous disease that clinically manifests as chronic inflammatory osteoarticular and dermatological lesions.
Chen Li +6 more
doaj +4 more sources
SAPHO Syndrome Presenting With Severe Inflammatory Back Pain (Sacroiliitis) and Rare Retinol Associated Myopathy in an Iraqi Adolescent Male: A Case Report and Literature Review [PDF]
SAPHO syndrome is a rare autoinflammatory disorder characterized by synovitis, acne, pustulosis, hyperostosis, and osteitis. Although musculoskeletal and dermatologic manifestations are well recognized, extra‐articular involvement remains uncommon ...
Farah Jaafar Mahdi +7 more
doaj +3 more sources
JAK Inhibitors for Treatment of SAPHO Syndrome: A Systematic Review of 72 Cases [PDF]
Objective Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome usually involves bones, joints, and skin. Due to a lack of known pathogenesis and clinical trials, there is no standard treatment of SAPHO syndrome.
Patrick Fazeli +9 more
doaj +3 more sources
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome, a type of chronic inflammatory disease, is rare and difficult to treat. Osteoarthropathy with skin involvement is the primary clinical manifestation of SAPHO syndrome.
Fangfang Yuan, Jing Luo, Qiong Yang
doaj +3 more sources
Evaluation of tonsillectomy in the treatment of SAPHO syndrome: past evidence and future directions [PDF]
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a rare aseptic inflammatory clinical syndrome characterized by widespread skin lesions and bone-joint lesions.
Wen-Yuan Gan +3 more
doaj +2 more sources
Upadacitinib in the treatment of SAPHO syndrome: a case report [PDF]
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome, a rare autoinflammatory disease, is usually defined by musculoskeletal symptoms and cutaneous manifestations.
Yanran Yang, Zhanxue Sun, Yongpeng Ge
doaj +2 more sources
Clinical Images: Successfully treated mandibular osteomyelitis by tumor necrosis factor inhibitor in SAPHO syndrome. [PDF]
Arthritis &Rheumatology, Volume 78, Issue 4, Page 993-994, April 2026.
Oba S +5 more
europepmc +2 more sources
Postpartum lumbopelvic pain could be SAPHO syndrome: a case report [PDF]
BackgroundSynovitis–acne–pustulosis–hyperostosis–osteitis (SAPHO) syndrome is a rare autoimmune disorder. The involvement of spinal and sacroiliac joint in SAPHO syndrome closely resembles the manifestations of postpartum lumbopelvic pain (LPP).Case ...
Zheng Weiwei, Zhang Junhong, Zhang Rong
doaj +2 more sources
The role of cytokines in the pathogenesis of SAPHO syndrome [PDF]
SAPHO syndrome is a complex inflammatory disorder affecting the skin and bones, characterized by osteomyelitis, acne, and pustulosis. Cytokines play a pivotal role in the pathogenesis of SAPHO syndrome, especially in inflammatory responses and immune ...
Yi Yang +5 more
doaj +2 more sources
Familial clustering of SAPHO syndrome. [PDF]
In a novel investigation of familial aggregation in SAPHO syndrome, a rare chronic autoinflammatory disorder characterized by the acronym synovitis, acne, pustulosis, hyperostosis, and osteitis, we identified a unique familial cohort with four affected individuals, including a male, marking the first report of male familial involvement in the ...
Gu M +5 more
europepmc +4 more sources

