Literature DB >> 24797142

[SAPHO syndrome].

I Gharsallah1, A Souissi2, R Dhahri3, N Boussetta4, S Sayeh3, L Métoui3, F Ajili4, B Louzir4, S Othmani4.   

Abstract

SAPHO (synovitis, acne, pustulosis, hyperostosis, osteitis) syndrome is a rare entity characterized by the association of heterogeneous osteoarticular and cutaneous manifestations that have for common denominator an aseptic inflammatory process. The etiopathogeny of this disease is still a matter of debate. Although it has been related to the spondylarthritis family, an infectious origin is suggested. Diagnosis is based on the presence of at least one of the three diagnostic criteria proposed by Kahn. The treatment includes NSAIDs, antibiotics, corticosteroids, methotrexate and more recently the bisphosphonates and the TNFα inhibitors.
Copyright © 2014 Société nationale française de médecine interne (SNFMI). Published by Elsevier SAS. All rights reserved.

Entities:  

Keywords:  Acne; Acné; Pustulose; Pustulosis; SAPHO; Spondylarthropathies; Spondyloarthropathies

Mesh:

Year:  2014        PMID: 24797142     DOI: 10.1016/j.revmed.2013.12.018

Source DB:  PubMed          Journal:  Rev Med Interne        ISSN: 0248-8663            Impact factor:   0.728


  1 in total

1.  Orofacial manifestations of SAPHO syndrome: a systematic review of case reports.

Authors:  Clémence Ferreira-Vilaca; Leonor Costa Mendes; Sophie-Caroline Campana; Isabelle Bailleul-Forestier; Christine Audouin-Pajot; Rémi Esclassan; Thibault Canceill
Journal:  Clin Rheumatol       Date:  2020-05-09       Impact factor: 2.980

  1 in total

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