| dc.contributor.author | Gurkanlar, D. | |
| dc.contributor.author | Kocak, H. | |
| dc.contributor.author | Yucel, E. | |
| dc.contributor.author | Aciduman, A. | |
| dc.contributor.author | Gunaydin, A. | |
| dc.contributor.author | Ekinci, Oe. | |
| dc.contributor.author | Keskil, S. | |
| dc.date.accessioned | 2020-06-25T17:43:53Z | |
| dc.date.available | 2020-06-25T17:43:53Z | |
| dc.date.issued | 2007 | |
| dc.identifier.issn | 1130-1473 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12587/3935 | |
| dc.description | WOS: 000247859000007 | en_US |
| dc.description | PubMed: 17497058 | en_US |
| dc.description.abstract | Gangliogliomas represent only 0.4% of central nervous system neoplasms and 1.3% of brain tumors. They are benign neoplasms with low morbidity and mortality and the patients usually present with seizures, but there has been no adult ganglioglioma with lytic skull lesion. A 49-year-old right handed woman suffering from generalized epileptic seizures was admitted to our hospital. She had also left hemiparesis with 4/5 motor strength. Magnetic resonance imaging and immunohistochemical studies revealed WHO Grade 11 ganglioglioma. Skull X-ray showed the lytic skull lesions. We have to consider gangliogliomas in the differential diagnosis of lytic skull lesions. | en_US |
| dc.language.iso | spa | en_US |
| dc.publisher | Sociedad Espanola Neurocirugia | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | ganglioglioma | en_US |
| dc.subject | lytic skull lesions | en_US |
| dc.subject | sinaptophysin | en_US |
| dc.title | Ganglioglioma with lytic skull lesions: a case report | en_US |
| dc.type | article | en_US |
| dc.identifier.volume | 18 | en_US |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.startpage | 123 | en_US |
| dc.identifier.endpage | 126 | en_US |
| dc.relation.journal | Neurocirugia | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
