Adrenal Ganglioneuroma: Case Report

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dc.authoridDokmetas, Hatice Sebile/0000-0003-0300-4173
dc.contributor.authorKilicli, Fatih
dc.contributor.authorAcibucu, Feffah
dc.contributor.authorDokmetas, Hatice Sebila
dc.contributor.authorElagoz, Sahande
dc.contributor.authorGokce, Gokhan
dc.contributor.authorOztoprak, Ibrahim
dc.date.accessioned2024-10-26T18:03:56Z
dc.date.available2024-10-26T18:03:56Z
dc.date.issued2011
dc.departmentSivas Cumhuriyet Üniversitesi
dc.description.abstractGanglioneuroma (ON) is a rare benign tumor arising mainly from neural crest cells and consisting of Schwann and ganglion cells. GN rarely occurs from the adrenal medulla and is observed most commonly in children and young adults. It is not associated with hormonal activity and is clinically asymptomatic. We present a 35-year-old woman whose abdominal ultrasonography for abdominal pain revealed in the right adrenal gland, a biochemically normal mass that was minimally hypointense on Tl-weighted and hyperintense on T2-weighted magnetic resonance images (MRI) and which was pathologically diagnosed as GN after adrenalectomy.
dc.identifier.endpage76
dc.identifier.issn1301-2193
dc.identifier.issue3
dc.identifier.scopus2-s2.0-84856866220
dc.identifier.scopusqualityQ4
dc.identifier.startpage74
dc.identifier.urihttps://hdl.handle.net/20.500.12418/28668
dc.identifier.volume15
dc.identifier.wosWOS:000217315800007
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherGalenos Yayincilik
dc.relation.ispartofTurkish Journal of Endocrinology and Metabolism
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAdrenal gland
dc.subjectganglioneuroma
dc.subjectmagnetic resonance imaging
dc.titleAdrenal Ganglioneuroma: Case Report
dc.typeArticle

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