Publication:
Long-Time Survival in a Patient with Turcot Syndrome Diagnosed in the Fifth Decade: Case Report

dc.authorscopusid6507281721
dc.authorscopusid11540148200
dc.authorscopusid19640258900
dc.authorscopusid35105726100
dc.authorscopusid35579498900
dc.authorscopusid36702709300
dc.contributor.authorMeydan, D.
dc.contributor.authorGürsel, B.
dc.contributor.authorOkumus, N.
dc.contributor.authorOdabaşı, E.
dc.contributor.authorYildiz, L.
dc.contributor.authorDemirag̈, G.G.
dc.date.accessioned2025-12-10T22:10:43Z
dc.date.issued2011
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Meydan] Ahmet Deniz, Department of Radiation Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Gürsel] Bilge, Department of Radiation Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Okumus̈] Nilgün Özbek, Department of Radiation Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Odabaşı] Eylem Aliş, Department of Radiation Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yíldíz] Levent, Department of Pathology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Demirag̈] Güzin Gonullu, Department of Medical Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractTurcot syndrome is a rare inherited disorder characterized by the association of colon and central nervous system neuroepithelial tumors. Here, we present a patient with Turcot Syndrome having glioblastoma together with colon adeno carcinoma. The patient, 47 year-old male, was referred to our department for cranial radiotherapy after gross-total resection of primary brain tumor in October 2003. During clinical follow-up in October 2004 a right colon mass was determined and right hemicolectomy was performed. Six courses of adjuvant chemotherapy were applied after resection. The patient is still under follow-up without any recurrences or metastasis. He has also first-degree relatives with colon cancer in his family's history. It has been declared that patients with Turcot Syndrome, who have high-grade glial tumor, survive longer than other brain tumor patients. With some certain exceptions, all these patients were young. There are few patients who were diagnosed of glioblastoma at the fifth decade and had long survival period. Present case is elderly diagnosed with Turcot syndrome and has long survival for glioblastoma, therefore, it is a rare clinical manifestation of Turcot Syndrome.en_US
dc.identifier.endpage96en_US
dc.identifier.issn1300-1817
dc.identifier.issn1302-1664
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-79953749962
dc.identifier.scopusqualityN/A
dc.identifier.startpage91en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/35000
dc.identifier.volume28en_US
dc.identifier.wosqualityN/A
dc.language.isotren_US
dc.relation.ispartofJournal of Neurological Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectColon Carcinomaen_US
dc.subjectGlioblastomaen_US
dc.subjectTurcot Syndromeen_US
dc.titleLong-Time Survival in a Patient with Turcot Syndrome Diagnosed in the Fifth Decade: Case Reporten_US
dc.title.alternativeBeşinci Dekatta Turcot Sendromu Tanisi Almiş Bir Hastada Uzun Süreli Sağkalim: Olgu Sunumuen_US
dc.typeArticleen_US
dspace.entity.typePublication

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