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The dark side of SAPHO syndrome.

Authors :
Henriques CC
Sousa M
Panarra A
Riso N
Source :
BMJ case reports [BMJ Case Rep] 2011 Dec 21; Vol. 2011. Date of Electronic Publication: 2011 Dec 21.
Publication Year :
2011

Abstract

SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis and osteitis) is a relatively rare entity. The therapeutic approach of patients with SAPHO syndrome has included multiple drugs with varying success and incoherence responses. The therapy is still empirical today. SAPHO syndrome is commonly treated with non-steroidal anti-inflammatory drugs, bisphophonates and non-biologic disease modifying antirheumatic drugs. Recent reports showed successful treatment with tumour necrosis factor α (TNF α) antagonists, but there is still a dark side of SAPHO syndrome including a subgroup of patient's refractory to all the treatments that have been empirically experienced. A clinical report of a patient with SAPHO syndrome with 12 years of evolution is described. All the therapeutic approaches, including anti TNF α therapy, have not prevented the clinical and radiographic progression of the disease. Given that the disease affects mostly younger patients, new therapeutic strategies are necessary in order to avoid potentially irreversible joint and bone lesions.

Details

Language :
English
ISSN :
1757-790X
Volume :
2011
Database :
MEDLINE
Journal :
BMJ case reports
Publication Type :
Academic Journal
Accession number :
22670011
Full Text :
https://doi.org/10.1136/bcr.11.2011.5197