Results 1 to 10 of about 1,382 (156)

Family aggregation and prevalence of other autoimmune diseases in SAPHO syndrome [PDF]

open access: yesHeliyon, 2023
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]

open access: yesClinical Case Reports
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]

open access: yesACR Open Rheumatology
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

SAPHO Syndrome Complicated by Ankylosing Spondylitis Successfully Treated With Tofacitinib: A Case Report

open access: yesFrontiers in Immunology, 2022
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]

open access: yesFrontiers in Medicine
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]

open access: yesFrontiers in Immunology
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]

open access: yesArthritis Rheumatol
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]

open access: yesFrontiers in Immunology
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]

open access: yesFrontiers in Immunology
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]

open access: yesCent Eur J Immunol
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

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