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dc.contributor.authorErol, Ozan
dc.contributor.authorKoycu, Alper
dc.contributor.authorAydin, Erdinc
dc.date.accessioned2019-06-20T11:07:17Z
dc.date.available2019-06-20T11:07:17Z
dc.date.issued2016
dc.identifier.issn2090-6765
dc.identifier.urihttps://www.hindawi.com/journals/criot/2016/1454932/abs/
dc.identifier.urihttp://hdl.handle.net/11727/3636
dc.description.abstractGanglioneuroblastoma is a rare tumor with moderate malignancy, which is composed of mature ganglion cells and seen in sympathetic ganglia and adrenal medulla. The diagnosis is possible after cytological and immunohistochemical studies following a needle biopsy or surgical excision. There is no consensus regarding the need for chemo-or radiotherapy after surgery. In this case report, clinical behavior and diagnosis and treatment of the rare tumor cervical ganglioneuroblastoma were discussed.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1155/2016/1454932en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectNEUROBLASTIC TUMORSen_US
dc.titleA Rare Tumor in the Cervical Sympathetic Trunk: Ganglioneuroblastomaen_US
dc.typearticleen_US
dc.relation.journalCASE REPORTS IN OTOLARYNGOLOGYen_US
dc.identifier.wos000388858900001en_US
dc.contributor.pubmedID27965907en_US
dc.contributor.orcID0000-0003-1290-3509en_US
dc.contributor.orcID0000-0001-6864-7378en_US
dc.contributor.orcID0000-0002-4209-9403en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.contributor.researcherIDAAF-3650-2021en_US
dc.contributor.researcherIDAAJ-2379-2021en_US


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