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The Dark Side of SAPHO Syndrome

dc.contributor.authorCoelho Henriques, C
dc.contributor.authorSousa, M
dc.contributor.authorPanarra, A
dc.contributor.authorRiso, N
dc.date.accessioned2018-05-23T10:12:09Z
dc.date.available2018-05-23T10:12:09Z
dc.date.issued2011-12-21
dc.description.abstractSAPHO 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.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBMJ Case Rep. 2011 Dec 21;2011. pii: bcr1120115197pt_PT
dc.identifier.doi10.1136/bcr.11.2011.5197pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/2980
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherBMJ Publishing Grouppt_PT
dc.subjectAdultpt_PT
dc.subjectDisease Progressionpt_PT
dc.subjectHumanspt_PT
dc.subjectMalept_PT
dc.subjectAcquired Hyperostosis Syndromept_PT
dc.subjectHCC MEDpt_PT
dc.titleThe Dark Side of SAPHO Syndromept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPagebcr1120115197pt_PT
oaire.citation.issuedec21 1pt_PT
oaire.citation.startPagebcr1120115197pt_PT
oaire.citation.titleBMJ Case Reportspt_PT
oaire.citation.volume2011pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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