Geniculo-temporo-parotideal neurofibroma of the facial nerve: A case report

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dc.authorid0000-0002-2572-0376
dc.authorid0000-0001-5428-0368
dc.authorid0000-0003-4096-4261
dc.contributor.authorYılmaz, Fahrettin
dc.contributor.authorGürel, Kamil
dc.contributor.authorGürel, Safiye
dc.contributor.authorSessiz N.
dc.contributor.authorBoran, Çetin
dc.date.accessioned2021-06-23T18:54:19Z
dc.date.available2021-06-23T18:54:19Z
dc.date.issued2006
dc.departmentBAİBÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.description.abstractPreoperative diagnosis of facial nerve neurofibroma is difficult when it presents as an asymptomatic parotideal mass. Facial nerve tumor suspicion arises during parotid surgery, histopathologic evaluation confirms diagnosis and postoperative imaging demonstrates a nerve tumor and its extension. We present the multimodality imaging findings of a 43-year-old man with a solitary neurofibroma involving the whole facial nerve continuously from geniculate ganglion to parotideal segment as the first case in the literature.en_US
dc.identifier.doi10.1177/197140090601900617
dc.identifier.endpage797en_US
dc.identifier.issn1971-4009
dc.identifier.issue6en_US
dc.identifier.scopus2-s2.0-33847012594en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage792en_US
dc.identifier.urihttps://doi.org/10.1177/197140090601900617
dc.identifier.urihttps://hdl.handle.net/20.500.12491/4371
dc.identifier.volume19en_US
dc.indekslendigikaynakScopusen_US
dc.institutionauthorYılmaz, Fahrettin
dc.institutionauthorGürel, Kamil
dc.institutionauthorGürel, Safiye
dc.institutionauthorSessiz N.
dc.institutionauthorBoran, Çetin
dc.language.isoenen_US
dc.publisherCentauro SRLen_US
dc.relation.ispartofNeuroradiology Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectFacial Nerveen_US
dc.subjectNeurofibromaen_US
dc.subjectParotid Glanden_US
dc.titleGeniculo-temporo-parotideal neurofibroma of the facial nerve: A case reporten_US
dc.typeArticleen_US

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