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Article

Rare occurrence of IDH2 mutation in adolescent oligodendroglioma with 1p/19q co-deletion: a case report.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery - 1 Dec 2020

Rao Shilpa, Sivakoti Sumitra, Arivazhagan Arimappamagan, Santosh Vani

Abstract excerpt

Adolescent and young adult gliomas are recently being studied as a distinct group and molecular alterations of oligodendroglioma in this group are not well defined. Few studies conducted on adolescent oligodendroglioma so far have found low frequencies of IDH mutations and 1p/19q co-deletion, which are the hallmark genetic alterations seen in adult oligodendroglioma. In this case report, we demonstrate presence...

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PMID: 32296936
DOI: 10.1007/s00381-020-04614-6

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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