Publication:
SAPHO syndrome: Misdiagnosed and operated [Sindrome de SAPHO: Mal diagnosticado e operado]

Simple item page
dc.contributor.authorsKaradag-Saygi E., Hakan Gunduz O., Gumrukcu G., Akyuz G.
dc.date.accessioned2022-03-28T14:55:01Z
dc.date.accessioned2026-01-11T05:57:57Z
dc.date.available2022-03-28T14:55:01Z
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.issn0303464X
dc.identifier.pubmed19078862
dc.identifier.urihttps://hdl.handle.net/11424/256204
dc.language.isopor
dc.relation.ispartofActa Reumatologica Portuguesa
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectMediastinal fibrosis
dc.subjectSAPHO syndrome
dc.subjectSweet's syndrome
dc.titleSAPHO syndrome: Misdiagnosed and operated [Sindrome de SAPHO: Mal diagnosticado e operado]
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage463
oaire.citation.issue4
oaire.citation.startPage460
oaire.citation.titleActa Reumatologica Portuguesa
oaire.citation.volume33

Files

Collections

Araştırma Çıktıları