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dc.contributor.authorBilginer, Burçak
dc.contributor.authorIsikay, Ilkay
dc.contributor.authorHanalioglu, Sahin
dc.contributor.authorBasar, Ibrahim
dc.contributor.authorNarin, Firat
dc.date.accessioned2020-12-07T12:21:19Z
dc.date.available2020-12-07T12:21:19Z
dc.date.issued2019
dc.identifier.citationIsikay I, Hanalioglu S, Basar I, Narin F, Bilginer B. Survival Benefit with Gross Total Resection and Adjuvant Radiotherapy in Childhood Atypical Teratoid/Rhabdoid Tumors: Results of a Single-Center Cohort of 27 Cases. Turk Neurosurg. 2019;29(5):689-697. doi: 10.5137/1019-5149.JTN.25406-18.1. PMID: 30875078.tr_TR
dc.identifier.issn‎2651-5032
dc.identifier.urihttp://www.turkishneurosurgery.org.tr/abstract.php?id=2221
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/30875078/
dc.identifier.urihttp://hdl.handle.net/11655/23163
dc.identifier.urihttps://doi.org/10.5137/1019-5149.jtn.25406-18.1
dc.description.abstractAim: To share a single center experience with 27 atypical teratoid/rhabdoid tumor (AT/RT) cases, and to determine the effect of gross total tumor resection and other clinical characteristics on the overall survival rate of AT/RT. Material and methods: We included 27 patients-with a histopathologically confirmed primary intracranial childhood AT/ RT-who were operated in our clinic between January 2000 and December 2017. Age, sex, tumor location, disseminated disease, the presence of hydrocephalus, symptom duration till diagnosis, the extent of resection, and adjuvant radiotherapy were evaluated for their influence on overall survival. Results: Median age at diagnosis for 27 patients was 19.1 months (7.2 months-5 years). Gross total resection was possible in 13 (48.72%) patients. Except for three patients who died of perioperative complications, all patients received chemotherapy and 11 received radiotherapy. In univariate analysis, male sex, older age at diagnosis (≥24 months), gross total resection, and radiotherapy were associated with overall longer survival; however, radiotherapy remained the only significant parameter in multivariate analysis. Conclusion: AT/RT is a rare and dreadful brain tumor that has low survival rates despite contemporary treatment. Radiotherapy seems to prolong survival; however, large-scale studies are needed to establish prognostic factors.tr_TR
dc.language.isoentr_TR
dc.publisherTurkish Neurosurgerytr_TR
dc.relation.isversionof10.5137/1019-5149.JTN.25406-18.1tr_TR
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.rightsAttribution 4.0 United States
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectRhabdoid tumortr_TR
dc.subjectObservational studytr_TR
dc.subjectChildhood Brain neoplasmstr_TR
dc.titleSurvival Benefit with Gross Total Resection and Adjuvant Radiotherapy in Childhood Atypical Teratoid/Rhabdoid Tumors: Results of a Single-Center Cohort of 27 Casestr_TR
dc.typeinfo:eu-repo/semantics/articletr_TR
dc.relation.journalTurkish Neurosurgerytr_TR
dc.contributor.departmentBeyin ve Sinir Cerrahisitr_TR
dc.identifier.volume29tr_TR
dc.identifier.issue5tr_TR
dc.identifier.startpage689tr_TR
dc.identifier.endpage697tr_TR
dc.description.indexWoStr_TR
dc.fundingYoktr_TR


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