Basit öğe kaydını göster

dc.contributor.authorIsikay, Ilkay
dc.contributor.authorHanalioglu, Sahin
dc.contributor.authorBasar, Ibrahim
dc.contributor.authorNarin, Firat
dc.contributor.authorBilginer, Burcak
dc.date.accessioned2021-06-03T06:15:49Z
dc.date.available2021-06-03T06:15:49Z
dc.date.issued2019
dc.identifier.issn1019-5149
dc.identifier.urihttp://dx.doi.org/10.5137/1019-5149.JTN.25406-18.1
dc.identifier.urihttp://hdl.handle.net/11655/24275
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.
dc.language.isoen
dc.relation.isversionof10.5137/1019-5149.JTN.25406-18.1
dc.rightsAttribution 4.0 United States
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectBrain neoplasms
dc.subjectChildhood
dc.subjectObservational study
dc.subjectRhabdoid tumor
dc.titleSurvival Benefit With Gross Total Resection And Adjuvant Radiotherapy In Childhood Atypical Teratoid/Rhabdoid Tumors: Results Of A Single-Center Cohort Of 27 Cases
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalTurkish Neurosurgery
dc.contributor.departmentBeyin ve Sinir Cerrahisi
dc.identifier.volume29
dc.identifier.issue5
dc.description.indexWoS
dc.description.indexScopus


Bu öğenin dosyaları:

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster

Attribution 4.0 United States
Aksi belirtilmediği sürece bu öğenin lisansı: Attribution 4.0 United States