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dc.contributor.authorOzer, Derda
dc.contributor.authorTuncer, Samuray
dc.date.accessioned2021-03-06T19:49:22Z
dc.date.available2021-03-06T19:49:22Z
dc.date.issued2015
dc.identifier.citationTuncer S., Ozer D., "Recent Trends in the Management of Retinoblastoma", TURK OFTALMOLOJI DERGISI-TURKISH JOURNAL OF OPHTHALMOLOGY, cilt.45, ss.71-76, 2015
dc.identifier.othervv_1032021
dc.identifier.otherav_f82fc73f-422a-449e-819f-adb13d5a0780
dc.identifier.urihttp://hdl.handle.net/20.500.12627/162593
dc.identifier.urihttps://doi.org/10.4274/tjo.26097
dc.description.abstractRetinoblastoma is the most common intraocular malignancy of childhood. Significant progress has been made in the past few years in the management of retinoblastoma. Thus, the patients' survival and ocular salvage rates have shown marked improvement. The current treatment strategies for retinoblastoma include enucleation, intravenous chemoreduction, and intra-arterial chemotherapy. Enucleation is generally reserved for eyes with extensive retinoblastoma, in which there is no hope for useful vision. From mid-1990s, intravenous chemoreduction has been used efficiently in the management of group A, B, or C, and some D eyes according to the International Classification of Retinoblastoma. Intravenous chemoreduction combined with focal treatments (cryotherapy, transpupillary thermotherapy, and brachytherapy) have provided favorable tumor control for most of these eyes. In 2008, superselective intra-arterial chemotherapy has been popularized. This treatment involves injection of a chemotherapeutic agent (mostly melphalan) after selective catheterization of the ophthalmic artery under neuroradiologic intervention. This provides higher success in advanced group D and Group E eyes that have relatively lower rate of tumor control with conventional intravenous chemoreduction. In conclusion, significant advances that have emerged recently in the management of retinoblastoma led to an increase in ocular salvage rates. Recently, popularized modality of intra-arterial chemotherapy offers hope in the control of eyes with advanced retinoblastoma.
dc.language.isoeng
dc.subjectTıp
dc.subjectGöz Hastalıkları ve Cerrahisi
dc.subjectSağlık Bilimleri
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectOFTALMOLOJİ
dc.titleRecent Trends in the Management of Retinoblastoma
dc.typeMakale
dc.relation.journalTURK OFTALMOLOJI DERGISI-TURKISH JOURNAL OF OPHTHALMOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume45
dc.identifier.issue2
dc.identifier.startpage71
dc.identifier.endpage76
dc.contributor.firstauthorID221521


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