Publication:
SAPHO syndrome: misdiagnosed and operated

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dc.contributor.authorsKaradag-Saygi, Evrim; Gunduz, O. Hakan; Gumrukcu, Gulistan; Akyuz, Gulseren
dc.date.accessioned2022-03-25T19:39:21Z
dc.date.accessioned2026-01-11T10:55:26Z
dc.date.available2022-03-25T19:39:21Z
dc.date.issued2008-12
dc.description.abstractSAPHO is a rare disorder that results in synovitis, acne, pustulosis, hyperostosis and osteitis. Patients with this syndrome typically present with musculoskeletal complaints, frequently localized to the anterior chest wall. However, diagnosis can be difficult in case of involvement of only one symptomatic bone without skin lesions. Awareness of SAPHO syndrome is necessary for accurate diagnosis and to prevent inappropriate and unnecessary treatment.
dc.identifier.issn0303-464X
dc.identifier.pubmedPMID: 19078862
dc.identifier.urihttps://hdl.handle.net/11424/254817
dc.language.isoeng
dc.relation.ispartofActa Reumatologica Portuguesa
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectFemale
dc.subjectHumans
dc.subjectMiddle Aged
dc.subjectDiagnosis, Differential
dc.subjectDiagnostic Errors
dc.subjectAcquired Hyperostosis Syndrome
dc.subjectHyperostosis, Sternocostoclavicular
dc.titleSAPHO syndrome: misdiagnosed and operated
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage463
oaire.citation.startPage460
oaire.citation.titleActa Reumatologica Portuguesa
oaire.citation.volume4

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