Cargando…

EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24)

BACKGROUND: We report a unique case of spinal ependymoma with classic histology and aggressive clinical behavior which harbored a focal MYC (8q24) amplification. CASE REPORT: A-12-year old male presented with a three months history of back pain and acute onset weakness with ataxia. A spine MRI revea...

Descripción completa

Detalles Bibliográficos
Autores principales: Shatara, Margaret, Boué, Daniel R, Pierson, Christopher R, Thomas, Diana L, Sribnick, Eric A, Jones, Jeremy, Rodriguez, Diana P, Schieffer, Kathleen M, Deeg, Carol, Hamelberg, Elizabeth, LaHaye, Stephanie, Magrini, Vincent, Wilson, Richard K, Mardis, Elaine R, Cottrell, Catherine E, Varga, Elizabeth A, AbdelBaki, Mohamed S, Finlay, Jonathan L, Osorio, Diana S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715824/
http://dx.doi.org/10.1093/neuonc/noaa222.165
_version_ 1783619046019694592
author Shatara, Margaret
Boué, Daniel R
Pierson, Christopher R
Thomas, Diana L
Sribnick, Eric A
Jones, Jeremy
Rodriguez, Diana P
Schieffer, Kathleen M
Deeg, Carol
Hamelberg, Elizabeth
LaHaye, Stephanie
Magrini, Vincent
Wilson, Richard K
Mardis, Elaine R
Cottrell, Catherine E
Varga, Elizabeth A
AbdelBaki, Mohamed S
Finlay, Jonathan L
Osorio, Diana S
author_facet Shatara, Margaret
Boué, Daniel R
Pierson, Christopher R
Thomas, Diana L
Sribnick, Eric A
Jones, Jeremy
Rodriguez, Diana P
Schieffer, Kathleen M
Deeg, Carol
Hamelberg, Elizabeth
LaHaye, Stephanie
Magrini, Vincent
Wilson, Richard K
Mardis, Elaine R
Cottrell, Catherine E
Varga, Elizabeth A
AbdelBaki, Mohamed S
Finlay, Jonathan L
Osorio, Diana S
author_sort Shatara, Margaret
collection PubMed
description BACKGROUND: We report a unique case of spinal ependymoma with classic histology and aggressive clinical behavior which harbored a focal MYC (8q24) amplification. CASE REPORT: A-12-year old male presented with a three months history of back pain and acute onset weakness with ataxia. A spine MRI revealed an avidly enhancing intradural, extramedullary mass occupying the dorsal spinal canal from C6 through T2. The tumor demonstrated mild diffusion restriction and was associated with severe cord compression and mild edema. He underwent gross total resection. Pathological diagnosis was classic grade II ependymoma. Eleven months later, he re-presented with acute onset lower extremity paresthesia and left-handed weakness. Spine MRI demonstrated tumor recurrence extending from C2 through T1-T2 with resultant severe cord compression, again demonstrating avid enhancement and restricted diffusion. He underwent subtotal resection of the mass and focal proton beam irradiation. MOLECULAR CHARACTERISTICS: The patient was enrolled on an institutional comprehensive genomic profiling protocol. The tumor’s copy number profile was complex, including homozygous loss of 17p and notably, amplification of the MYC oncogene. Using fluorescence in situ hybridization, we identified >20 copies of MYC in interphase cells, confirming the gene amplification, while two copies of MYCN (2p24) were seen. DNA methylation further classified this tumor as clustering near posterior fossa group A (score=0.6073) tumors. CONCLUSION: We report a unique case of an adolescent male with aggressive spinal ependymoma harboring focal MYC amplification. Testing for MYC amplification may be reasonable in newly-diagnosed spinal ependymomas to aid in characterization.
format Online
Article
Text
id pubmed-7715824
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77158242020-12-09 EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24) Shatara, Margaret Boué, Daniel R Pierson, Christopher R Thomas, Diana L Sribnick, Eric A Jones, Jeremy Rodriguez, Diana P Schieffer, Kathleen M Deeg, Carol Hamelberg, Elizabeth LaHaye, Stephanie Magrini, Vincent Wilson, Richard K Mardis, Elaine R Cottrell, Catherine E Varga, Elizabeth A AbdelBaki, Mohamed S Finlay, Jonathan L Osorio, Diana S Neuro Oncol Ependymoma BACKGROUND: We report a unique case of spinal ependymoma with classic histology and aggressive clinical behavior which harbored a focal MYC (8q24) amplification. CASE REPORT: A-12-year old male presented with a three months history of back pain and acute onset weakness with ataxia. A spine MRI revealed an avidly enhancing intradural, extramedullary mass occupying the dorsal spinal canal from C6 through T2. The tumor demonstrated mild diffusion restriction and was associated with severe cord compression and mild edema. He underwent gross total resection. Pathological diagnosis was classic grade II ependymoma. Eleven months later, he re-presented with acute onset lower extremity paresthesia and left-handed weakness. Spine MRI demonstrated tumor recurrence extending from C2 through T1-T2 with resultant severe cord compression, again demonstrating avid enhancement and restricted diffusion. He underwent subtotal resection of the mass and focal proton beam irradiation. MOLECULAR CHARACTERISTICS: The patient was enrolled on an institutional comprehensive genomic profiling protocol. The tumor’s copy number profile was complex, including homozygous loss of 17p and notably, amplification of the MYC oncogene. Using fluorescence in situ hybridization, we identified >20 copies of MYC in interphase cells, confirming the gene amplification, while two copies of MYCN (2p24) were seen. DNA methylation further classified this tumor as clustering near posterior fossa group A (score=0.6073) tumors. CONCLUSION: We report a unique case of an adolescent male with aggressive spinal ependymoma harboring focal MYC amplification. Testing for MYC amplification may be reasonable in newly-diagnosed spinal ependymomas to aid in characterization. Oxford University Press 2020-12-04 /pmc/articles/PMC7715824/ http://dx.doi.org/10.1093/neuonc/noaa222.165 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Ependymoma
Shatara, Margaret
Boué, Daniel R
Pierson, Christopher R
Thomas, Diana L
Sribnick, Eric A
Jones, Jeremy
Rodriguez, Diana P
Schieffer, Kathleen M
Deeg, Carol
Hamelberg, Elizabeth
LaHaye, Stephanie
Magrini, Vincent
Wilson, Richard K
Mardis, Elaine R
Cottrell, Catherine E
Varga, Elizabeth A
AbdelBaki, Mohamed S
Finlay, Jonathan L
Osorio, Diana S
EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24)
title EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24)
title_full EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24)
title_fullStr EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24)
title_full_unstemmed EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24)
title_short EPEN-28. NOVEL ONCOGENE AMPLIFICATION IN SPINAL EPENDYMOMA INVOLVING THE MYC LOCUS (8q24)
title_sort epen-28. novel oncogene amplification in spinal ependymoma involving the myc locus (8q24)
topic Ependymoma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715824/
http://dx.doi.org/10.1093/neuonc/noaa222.165
work_keys_str_mv AT shataramargaret epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT bouedanielr epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT piersonchristopherr epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT thomasdianal epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT sribnickerica epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT jonesjeremy epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT rodriguezdianap epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT schiefferkathleenm epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT deegcarol epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT hamelbergelizabeth epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT lahayestephanie epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT magrinivincent epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT wilsonrichardk epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT mardiselainer epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT cottrellcatherinee epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT vargaelizabetha epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT abdelbakimohameds epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT finlayjonathanl epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24
AT osoriodianas epen28noveloncogeneamplificationinspinalependymomainvolvingthemyclocus8q24