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dc.contributor.authorKULACOGLU, Sezer
dc.contributor.authorUNAL, Adnan
dc.contributor.authorOZLUGEDIK, Samet
dc.contributor.authorOZCAN, Muge
dc.contributor.authorTezer, Mesut Sabri
dc.date.accessioned2021-03-03T16:49:09Z
dc.date.available2021-03-03T16:49:09Z
dc.date.issued2006
dc.identifier.citationUNAL A., OZLUGEDIK S., Tezer M. S. , KULACOGLU S., OZCAN M., "An atypical esthesioneuroblastoma of the inferior nasal cavity and maxillary sinus: Report of a case", TUMORI, cilt.92, sa.5, ss.440-443, 2006
dc.identifier.issn0300-8916
dc.identifier.othervv_1032021
dc.identifier.otherav_4662ea24-2fe9-4628-b931-dccfd6b68197
dc.identifier.urihttp://hdl.handle.net/20.500.12627/50916
dc.description.abstractEsthesioneuroblastoma is a rare malignant tumor of the nasal cavity that originates from the olfactory epithelium. In this paper a very rare clinical presentation of this tumor is described. The tumor originated from the maxillary sinus and alveolar process, and was independent of the olfactory region. The patient was a 14-year-old girl presenting with facial swelling and nasal obstruction. Paranasal computed tomography showed a mass filling the right nasal cavity, infiltrating the alveolar process, eroding the anterior wall of the maxilla and invading the subcutaneous tissues of the cheek. Fine-needle aspiration and incisional biopsies identified an esthesioneuroblastoma. After neoadjuvant chemotherapy, we performed a right subtotal and left inferior maxillectomy and reconstructed the maxillary defect with a permanent obturator. At 2 years' follow-up the patient is free of recurrence.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectONKOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectOnkoloji
dc.titleAn atypical esthesioneuroblastoma of the inferior nasal cavity and maxillary sinus: Report of a case
dc.typeMakale
dc.relation.journalTUMORI
dc.contributor.department, ,
dc.identifier.volume92
dc.identifier.issue5
dc.identifier.startpage440
dc.identifier.endpage443
dc.contributor.firstauthorID104703


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