GORHAM-STOUT DISEASE OF THE HUMERUS

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dc.contributor.authorYalniz, E.
dc.contributor.authorAlicioglu, B.
dc.contributor.authorBenlier, E.
dc.contributor.authorYilmaz, B.
dc.contributor.authorAltaner, S.
dc.date.accessioned2024-06-12T10:54:59Z
dc.date.available2024-06-12T10:54:59Z
dc.date.issued2008
dc.departmentTrakya Üniversitesien_US
dc.description.abstractGorham-Stout disease is characterized by local proliferation of small vascular or lymphatic channels resulting in progressive destruction and resorption of bone. The etiology and pathogenesis of the disease remains mostly unknown, despite some 175 reported cases. A case of Gorham-Stout disease of the humerus in a 14-year-old boy is described. The patient presented with progressive pain and deformity of the right arm. Although the disease was described in different bones of the body its location in the humerus is rare. We report the natural history and clinical follow-up in a young patient. A fibular graft was performed but 10 months later, resorption and pathological fractures occurred again. This study presents the radiographic and MRI features of Gorham disease.en_US
dc.identifier.endpage17en_US
dc.identifier.issn1780-2393
dc.identifier.issue1en_US
dc.identifier.pmid18447124en_US
dc.identifier.startpage14en_US
dc.identifier.urihttps://hdl.handle.net/20.500.14551/19255
dc.identifier.volume91en_US
dc.identifier.wosWOS:000260089900003en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherAssoc Royal Soc Scientifiques Medicales Belgesen_US
dc.relation.ispartofJbr-Btren_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBonesen_US
dc.subjectDiseases - Bonesen_US
dc.subjectOsteolysis - Bonesen_US
dc.subjectMRen_US
dc.subjectShoulder Girdleen_US
dc.titleGORHAM-STOUT DISEASE OF THE HUMERUSen_US
dc.typeArticleen_US

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