| dc.contributor.author | Niyaz L. | |
| dc.contributor.author | Gunduz K. | |
| dc.contributor.author | Meco C. | |
| dc.contributor.author | Kankaya D. | |
| dc.date.accessioned | 2020-06-21T09:43:18Z | |
| dc.date.available | 2020-06-21T09:43:18Z | |
| dc.date.issued | 2015 | |
| dc.identifier.issn | 1049-2275 | |
| dc.identifier.uri | https://doi.org/10.1097/SCS.0000000000002114 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/5296 | |
| dc.description | PubMed: 26468842 | en_US |
| dc.description.abstract | Esthesioneuroblastoma is a rare malignant tumor of neuroectodermal origin. It usually presents with nonspecific symptoms, such as nasal obstruction, epistaxis, and pain, but has an aggressive course if the treatment is delayed. The authors report a case of esthesioneuroblastoma in a 47-year-old woman, treated with extensive surgical resection, radiotherapy, and chemotherapy. Despite intensive treatment, the patient developed a local recurrence with systemic metastasis and succumbed 4 months later. Copyright © 2015 Mutaz B. Habal, MD. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Lippincott Williams and Wilkins | en_US |
| dc.relation.isversionof | 10.1097/SCS.0000000000002114 | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Esthesioneuroblastoma | en_US |
| dc.subject | Orbital tumor | en_US |
| dc.title | Esthesioneuroblastoma with poor outcome despite extensive treatment | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 26 | en_US |
| dc.identifier.issue | 7 | en_US |
| dc.identifier.startpage | e615 | en_US |
| dc.identifier.endpage | e616 | en_US |
| dc.relation.journal | Journal of Craniofacial Surgery | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
