En coup de sabre accompanied by pachydermoperiostosis: a case report

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dc.contributor.authorOzdemir, M.
dc.contributor.authorYildirim, S.
dc.contributor.authorMevlitoglu, I.
dc.date.accessioned2020-03-26T17:17:24Z
dc.date.available2020-03-26T17:17:24Z
dc.date.issued2007
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractScleroderma en coup de sabre, a variant of localized scleroderma is a disorder characterized by fibrosis of connective tissue. We report a 21-year-old female with scleroderma en coup de sabre accompanied by pachydermoperiostosis. She was born to consanguineous parents and her older siser also had pachydermoperiostosis characterized by clubbing of the digits, enlargement of distal parts of the extremities. The two disorders were diagnosed by clinical examination, histological and x-ray findings. In contrast to scleroderma, pachydermoperiostosis is a hypertrophic process characterized by periosteal proliferation of the tubuler bones and hypertrophic skin changes. We discuss this interesting coexistence and review the literature.en_US
dc.identifier.endpage317en_US
dc.identifier.issn0392-856Xen_US
dc.identifier.issn1593-098Xen_US
dc.identifier.issue2en_US
dc.identifier.pmid17543162en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage315en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/21382
dc.identifier.volume25en_US
dc.identifier.wosWOS:000246882200230en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherCLINICAL & EXPER RHEUMATOLOGYen_US
dc.relation.ispartofCLINICAL AND EXPERIMENTAL RHEUMATOLOGYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjecten coup de sabreen_US
dc.subjectpachydermoperiostosisen_US
dc.subjecthuman fibrosisen_US
dc.titleEn coup de sabre accompanied by pachydermoperiostosis: a case reporten_US
dc.typeArticleen_US

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