| Literature DB >> 29502353 |
Nitya Prabhakaran1, Miguel A Guzman2, Pournima Navalkele3, Edna Chow-Maneval4, Jacqueline R Batanian5.
Abstract
Gangliogliomas are rare neoplasms of the central nervous system that mostly originate in the temporal lobe and are associated with seizures. Literature mentions that BRAF mutations are most commonly associated with gangliogliomas. We discuss a unique case of ganglioglioma originating in the posterior fossa that showed multiple losses and a unique interstitial deletion at 9q21 by an array-comparative genome hybridization (array-CGH). The deletion led to a novel molecular fusion (TLE4-NTRK2) which was confirmed by next generation sequencing and provides a potential for a gene-targeted therapy.Entities:
Keywords: NTRK fusions; deletion; ganglioglioma; microarray; targeted therapy
Year: 2018 PMID: 29502353 DOI: 10.1111/neup.12458
Source DB: PubMed Journal: Neuropathology ISSN: 0919-6544 Impact factor: 1.906