Retinoblastoma, the visible CNS tumor: A review.

التفاصيل البيبلوغرافية
العنوان: Retinoblastoma, the visible CNS tumor: A review.
المؤلفون: Dimaras, H, Corson, TW
بيانات النشر: University of Nairobi
سنة النشر: 2018
المجموعة: University of Nairobi Digital Repository
مصطلحات موضوعية: MYCN, cancer genetics, neuroimaging, optical coherence tomography, pediatric cancer, pineoblastoma
الوصف: The pediatric ocular cancer retinoblastoma is the only central nervous system (CNS) tumor readily observed without specialized equipment: it can be seen by, and in, the naked eye. This accessibility enables unique imaging modalities. Here, we review this cancer for a neuroscience audience, highlighting these clinical and research imaging options, including fundus imaging, optical coherence tomography, ultrasound, and magnetic resonance imaging. We also discuss the subtype of retinoblastoma driven by the MYCN oncogene more commonly associated with neuroblastoma, and consider trilateral retinoblastoma, in which an intracranial tumor arises along with ocular tumors in patients with germline RB1 gene mutations. Retinoblastoma research and clinical care can offer insights applicable to CNS malignancies, and also benefit from approaches developed elsewhere in the CNS.
نوع الوثيقة: other/unknown material
وصف الملف: application/pdf
اللغة: English
العلاقة: Dimaras, Helen, and Timothy W. Corson. "Retinoblastoma, the visible CNS tumor: A review." Journal of Neuroscience Research.; https://www.ncbi.nlm.nih.gov/pubmed/29314142Test; http://hdl.handle.net/11295/102340Test
الإتاحة: http://hdl.handle.net/11295/102340Test
https://www.ncbi.nlm.nih.gov/pubmed/29314142Test
حقوق: Attribution-NonCommercial-NoDerivs 3.0 United States ; http://creativecommons.org/licenses/by-nc-nd/3.0/usTest/
رقم الانضمام: edsbas.42CE4F2C
قاعدة البيانات: BASE