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SAPHO syndrome and pustulotic arthro-osteitis
Mitsumasa Kishimoto1, Yoshinori Taniguchi2, Shigeyoshi Tsuji3
1Department of Nephrology and Rheumatology, Kyorin University School of Medicine, Tokyo, Japan.
Synovitis-Acne-Pustulosis-Hyperostosis-Osteitis (SAPHO) syndrome is a rare inflammatory condition. This review covers its musculoskeletal features, diagnosis, and management strategies for improving patient quality of life.
Area of Science:
- Rheumatology
- Dermatology
- Osteoarticular Disorders
Background:
- Synovitis-Acne-Pustulosis-Hyperostosis-Osteitis (SAPHO) syndrome is a rare inflammatory osteoarticular disorder.
- It encompasses conditions like pustulotic arthro-osteitis (PAO), characterized by osteitis, synovitis, and hyperostosis.
- SAPHO syndrome and PAO predominantly affect individuals aged 30-50, with a female predominance.
Purpose of the Study:
- To review the clinical, radiological, and laboratory features of SAPHO syndrome.
- To outline diagnostic criteria for SAPHO syndrome and PAO.
- To discuss non-pharmacological and pharmacological management strategies.
Main Methods:
- Literature review of SAPHO syndrome and related conditions.
- Analysis of epidemiological data, including prevalence and demographics.
- Summary of diagnostic approaches and treatment goals.
Main Results:
- PAO is a significant component of SAPHO syndrome, particularly in Japan.
- Severe acne is a common skin manifestation in SAPHO patients, especially in Israel.
- Prevalence data for SAPHO syndrome is limited, but palmoplantar pustulosis (PPP) affects 0.12% in Japan, with 10-30% of PPP patients having PAO.
Conclusions:
- Effective diagnosis relies on identifying diverse clinical, radiological, and laboratory features.
- Treatment aims to enhance quality of life, prevent structural damage, and restore physical and social function.
- Comprehensive management involves both non-pharmacological and pharmacological interventions.
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