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Rarest of the rare: Chordoid glioma infiltrating the optic chiasm

BACKGROUND: Chordoid glioma is a rare brain tumor typically located within the anterior third ventricle. It is a well-circumscribed, non-infiltrative tumor that grows as a mass within the ventricle. CASE DESCRIPTION: We present the case of a 50-year-old woman with a chordoid glioma located in the an...

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Detalles Bibliográficos
Autores principales: Al Hinai, Qasim S., Petrecca, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114368/
https://www.ncbi.nlm.nih.gov/pubmed/21697970
http://dx.doi.org/10.4103/2152-7806.80118
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author Al Hinai, Qasim S.
Petrecca, Kevin
author_facet Al Hinai, Qasim S.
Petrecca, Kevin
author_sort Al Hinai, Qasim S.
collection PubMed
description BACKGROUND: Chordoid glioma is a rare brain tumor typically located within the anterior third ventricle. It is a well-circumscribed, non-infiltrative tumor that grows as a mass within the ventricle. CASE DESCRIPTION: We present the case of a 50-year-old woman with a chordoid glioma located in the anterior third ventricle. Unusually, MRI revealed an enlarged optic chiasm. Histological sampling of the chiasm revealed tumor invasion. CONCLUSION: Involvement of the optic apparatus is generally thought to be an imaging feature that can be used to distinguish chordoid gliomas from optic/hypothalamic gliomas. This case provides the first reported exception to this dogma.
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spelling pubmed-31143682011-06-22 Rarest of the rare: Chordoid glioma infiltrating the optic chiasm Al Hinai, Qasim S. Petrecca, Kevin Surg Neurol Int Case Report BACKGROUND: Chordoid glioma is a rare brain tumor typically located within the anterior third ventricle. It is a well-circumscribed, non-infiltrative tumor that grows as a mass within the ventricle. CASE DESCRIPTION: We present the case of a 50-year-old woman with a chordoid glioma located in the anterior third ventricle. Unusually, MRI revealed an enlarged optic chiasm. Histological sampling of the chiasm revealed tumor invasion. CONCLUSION: Involvement of the optic apparatus is generally thought to be an imaging feature that can be used to distinguish chordoid gliomas from optic/hypothalamic gliomas. This case provides the first reported exception to this dogma. Medknow Publications Pvt Ltd 2011-04-28 /pmc/articles/PMC3114368/ /pubmed/21697970 http://dx.doi.org/10.4103/2152-7806.80118 Text en Copyright: y© 2011 Al Hinai QS. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Al Hinai, Qasim S.
Petrecca, Kevin
Rarest of the rare: Chordoid glioma infiltrating the optic chiasm
title Rarest of the rare: Chordoid glioma infiltrating the optic chiasm
title_full Rarest of the rare: Chordoid glioma infiltrating the optic chiasm
title_fullStr Rarest of the rare: Chordoid glioma infiltrating the optic chiasm
title_full_unstemmed Rarest of the rare: Chordoid glioma infiltrating the optic chiasm
title_short Rarest of the rare: Chordoid glioma infiltrating the optic chiasm
title_sort rarest of the rare: chordoid glioma infiltrating the optic chiasm
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114368/
https://www.ncbi.nlm.nih.gov/pubmed/21697970
http://dx.doi.org/10.4103/2152-7806.80118
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