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dc.contributor.authorBiltekin, Fatih
dc.contributor.authorYildiz, Demet
dc.contributor.authorOzyigit, Gokhan
dc.date.accessioned2019-12-10T11:30:44Z
dc.date.available2019-12-10T11:30:44Z
dc.date.issued2013
dc.identifier.issn1306-133X
dc.identifier.urihttps://doi.org/10.4999/uhod.12054
dc.identifier.urihttp://hdl.handle.net/11655/15804
dc.description.abstractNowadays, the use of computed tomography (CT) simulation is getting widespread with the use of new treatment modalities like three dimensional conformal radiotherapy (3D-CRT), intensity modulated radiotherapy (IMRT), adaptive radiotherapy (ART) and stereotactic radiosurgery (SRS) in radiotherapy facilities. The main purpose of these new treatment modalities are to increase the survival and increase the quality of life by reducing the side effects. However, radiation induced secondary malignancy risk is getting important after radiotherapy with the increase in survival. Especially, CT scanning was performed from head to sacral region for 3D-CRT craniospinal treatments techniques in children or young patients and several precautions should be taken to reduce the radiation dose due to the CT simulation. In this study, we measured organ equivalent dose in Alderson Rando phantom and we estimate radiation-induced cancer risk due to CT scanning for different conditions. According to our measurement, secondary malignancy risk was found to be between 0.10% - 0.22% for different conditions in craniospinal CT simulation.
dc.language.isoen
dc.publisherAkad Doktorlar Yayınevi
dc.relation.isversionof10.4999/uhod.12054
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectOncology
dc.titleEvaluation Of Secondary Malignancy Risk Due To The Whole Body Computerized Tomography Simulation In Radiotherapy Facilitiestr_en
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalUhod-Uluslararasi Hematoloji-Onkoloji Dergisi
dc.contributor.departmentRadyasyon Onkolojisi
dc.identifier.volume23
dc.identifier.issue4
dc.identifier.startpage250
dc.identifier.endpage253
dc.description.indexWoS
dc.description.indexScopus


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