Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/5809
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dc.contributor.authorDorwal, Pranav-
dc.contributor.authorWhite, Christine-
dc.contributor.authorGoh, Anna Fn-
dc.contributor.authorKumar, Amit-
dc.contributor.authorMcEniery, Jane-
dc.contributor.authorWalker, Rick-
dc.contributor.authorRobertson, Thomas-
dc.date.accessioned2024-06-20T00:27:43Z-
dc.date.available2024-06-20T00:27:43Z-
dc.date.issued2023-
dc.identifier.citationNeuropathology : official journal of the Japanese Society of Neuropathology, 2023en
dc.identifier.urihttps://dora.health.qld.gov.au/qldresearchjspui/handle/1/5809-
dc.description.abstractEpendymal tumors are classified based on their location, histology, and molecular characteristics. Supratentorial ependymomas (ST-EPNs) are a group of circumscribed supratentorial gliomas, which usually have pathogenic fusions involving either zinc finger translocation associated (ZFTA) (formerly C11orf95) or YAP1. A subtype of ependymoma was recently described and labeled ependymoma-like tumors with mesenchymal differentiation (ELTMDs). We describe a case of a 5-year-old boy who presented with a right frontal tumor. The diagnosis was challenging, and a correct diagnosis could only be reached after reanalysis of methylation data with a more recent version of the classifier and RNA fusion testing, which revealed ZFTA:NCOA1 (nuclear receptor coactivator 1) fusion. There are only a handful of cases of this entity, which is being reported for its rarity and the diagnostic challenge it poses. (© 2023 The Authors. Neuropathology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Neuropathology.)-
dc.titleEpendymoma-like tumor with mesenchymal differentiation (ELTMD) with ZFTA:NCOA1 fusion: A diagnostic challenge-
dc.identifier.doi10.1111/neup.12952-
dc.relation.urlhttps://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=mdc&AN=37931917&site=ehost-live-
dc.identifier.journaltitleNeuropathology : official journal of the Japanese Society of Neuropathology-
dc.identifier.risid4083-
item.grantfulltextnone-
item.fulltextNo Fulltext-
Appears in Sites:Children's Health Queensland Publications
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