Atypical central neurocytoma with novel EWSR1-ATF1 fusion and MUTYH mutation detected by next-generation sequencing

We present the case of a 13-year-old boy with a very unusual periventricular atypical central neurocytoma with unique molecular features treated with subtotal surgical resection and photon intensity-modulated radiotherapy. Histological features were most consistent with atypical central neurocytoma....

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Bibliografiske detaljer
Udgivet i:BMJ Case Rep
Main Authors: Aghajan, Yasmin, Malicki, Denise M, Levy, Michael L, Crawford, John Ross
Format: Artigo
Sprog:Inglês
Udgivet: BMJ Publishing Group 2019
Fag:
Rare Disease
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6340561/
https://ncbi.nlm.nih.gov/pubmed/30642852
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2018-226455
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