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Budny Agnieszka, Grochowski Cezary. Retinoblastoma. Journal of Education, Health and Sport. 2018;8(7):204-213. eISNN 2391-8306. DOI http://dx.doi.org/10.5281/zenodo.1299573 http://ojs.ukw.edu.pl/index.php/johs/article/view/5611 https://pbn.nauka.gov.pl/sedno-webapp/works/868825 The journal has had 7 points in Ministry of Science and Higher Education parametric evaluation. Part b item 1223 (26/01/2017). 1223 Journal of Education, Health and Sport eissn 2391-8306 7 © The Authors 2018; This article is published with open access at Licensee Open Journal Systems of Kazimierz Wielki University in Bydgoszcz, Poland Open Access. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author (s) and source are credited. This is an open access article licensed under the terms of the Creative Commons Attribution Non commercial license Share alike. (http://creativecommons.org/licenses/by-nc-sa/4.0/) which permits unrestricted, non commercial use, distribution and reproduction in any medium, provided the work is properly cited. The authors declare that there is no conflict of interests regarding the publication of this paper. Received: 02.05.2018. Revised: 18.05.2018. Accepted: 28.06.2018. Retinoblastoma Agnieszka Budny1, Cezary Grochowski2 1Radiotherapy Department, St. John’s Cancer Center, Lublin, Poland 2Neurosurgery and Pediatric Neurosurgery Department, Medical University of Lublin, Poland Introduction Retinoblastoma is a tumor originating from the nuclear layer of the primary retinal photoreceptor cells, genetically determined. It develops due to a mutation in chromosome 13 in the q14 band. It is the most common, originally malignant intraocular change in childhood and accounts for 10-15% of cancer cases occurring in the first year of life [1]. Usually this cancer manifests itself as a leukocoria in a child under two years of age. In a congenital form, it can be multifocal, on both sides, and the risk of secondary cancers should also be taken into account. Diagnosis of retinoblastoma requires indirect ophthalmoscopy and research using imaging diagnostics techniques: ultrasonography (USG), magnetic resonance imaging (MRI) or computed tomography (CT). If left untreated, it leads to metastasis and death of the child. With the advancement of medicine, survival with modern treatment methods is> 95%. More and more often it is possible to save the mutant eye enucleation surgery. Immediate referral to an ophthalmologist's oncologist and proper management by an interdisciplinary team are necessary to optimize the visual effect and survival [2]. |
