Publication:
SAPHO SYNDROME: MISDIAGNOSED AND OPERATED

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dc.contributor.authorsKaradag-Saygi, Evrim; Gunduz, O. Hakan; Gumrukcu, Gulistan; Akyuz, Gulseren
dc.date.accessioned2022-03-12T17:34:10Z
dc.date.accessioned2026-01-11T10:45:19Z
dc.date.available2022-03-12T17:34:10Z
dc.date.issued2008
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.doidoiWOS:000262022800013
dc.identifier.issn0303-464X
dc.identifier.pubmed19078862
dc.identifier.urihttps://hdl.handle.net/11424/228980
dc.identifier.wosWOS:000262022800013
dc.language.isoeng
dc.publisherPUBLISAUDE-EDICOES MEDICAS LDA
dc.relation.ispartofACTA REUMATOLOGICA PORTUGUESA
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectSAPHO Syndrome
dc.subjectMediastinal Fibrosis
dc.subjectSweet's Syndrome
dc.subjectOSTEITIS
dc.titleSAPHO SYNDROME: MISDIAGNOSED AND OPERATED
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage463
oaire.citation.issue4
oaire.citation.startPage460
oaire.citation.titleACTA REUMATOLOGICA PORTUGUESA
oaire.citation.volume33

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