Article
Secondary enucleated retinoblastoma with MYCN amplification.
Ophthalmic genetics - 1 Jun 2021
Moulin Alexandre P, Stathopoulos Christina, Marcelli Fabienne, Schoumans Pouw Jacqueline, Beck-Popovic Maja, Munier Francis L
Abstract excerpt
Background: Absence of RB1 mutation is rare in retinoblastoma and MYCN amplifications were recently identified in a subset of aggressive retinoblastomas occurring in infants. Here we describe not only the clinical phenotype of MYCN retinoblastoma at presentation, but also the tumor response to the first attempt of conservative management in this context.Methods: Interventional retrospective case reportResults: A...
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