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dc.contributor.authorIslak, C
dc.contributor.authorUrger, E
dc.contributor.authorKafadar, A
dc.contributor.authorKocer, N
dc.contributor.authorOz, B
dc.contributor.authorAlbayram, S
dc.date.accessioned2021-03-05T11:00:20Z
dc.date.available2021-03-05T11:00:20Z
dc.date.issued2005
dc.identifier.citationAlbayram S., Urger E., Oz B., Kafadar A., Islak C., Kocer N., "MR imaging of pial melanosis secondary to a posterior fossa melanotic ependymoma", AMERICAN JOURNAL OF NEURORADIOLOGY, cilt.26, ss.804-808, 2005
dc.identifier.issn0195-6108
dc.identifier.othervv_1032021
dc.identifier.otherav_a605555a-c8ed-49ce-a745-ab58f47fddf3
dc.identifier.urihttp://hdl.handle.net/20.500.12627/111025
dc.description.abstractA 36-year-old man presented with trouble speaking and bilateral progressive hearing loss. MR imaging and histopathologic results revealed a posterior fossa melanotic ependymoma. Pial surfaces appeared hyperintense on T1-weighted images and hypointense on T2-weighted images. Histopathologic examination revealed that tumor cells and interstitial spaces had abundant melanin accumulation. There was no evidence of hemosiderin in tumor cells and in interstitial spaces. Pial melanin accumulation secondary to a posterior fossa melanotic ependymoma explained our MR findings.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectNükleer Tıp
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectRADYOLOJİ, NÜKLEER TIP ve MEDİKAL GÖRÜNTÜLEME
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectSinirbilim ve Davranış
dc.subjectNÖRO-GÖRÜNTÜLEME
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleMR imaging of pial melanosis secondary to a posterior fossa melanotic ependymoma
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF NEURORADIOLOGY
dc.contributor.department, ,
dc.identifier.volume26
dc.identifier.issue4
dc.identifier.startpage804
dc.identifier.endpage808
dc.contributor.firstauthorID174847


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