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Holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature

Widespread primary spinal oligodendrogliomas are a rare variety of tumors that usually affect children. Currently, there are only two adult cases reported worldwide. We report the first case of primary holocord oligodendroglioma with intracranial extension in a young adult female. The patient presen...

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Autores principales: Cruz, Romulus Emmanuel H, De Roxas, Ranhel C, Sales-Callangan, Carmela Concepcion A, Jamora, Roland Dominic G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001686/
https://www.ncbi.nlm.nih.gov/pubmed/29390865
http://dx.doi.org/10.2217/cns-2017-0012
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author Cruz, Romulus Emmanuel H
De Roxas, Ranhel C
Sales-Callangan, Carmela Concepcion A
Jamora, Roland Dominic G
author_facet Cruz, Romulus Emmanuel H
De Roxas, Ranhel C
Sales-Callangan, Carmela Concepcion A
Jamora, Roland Dominic G
author_sort Cruz, Romulus Emmanuel H
collection PubMed
description Widespread primary spinal oligodendrogliomas are a rare variety of tumors that usually affect children. Currently, there are only two adult cases reported worldwide. We report the first case of primary holocord oligodendroglioma with intracranial extension in a young adult female. The patient presented with a 4-month history of fluctuating hemiparesis of the left upper extremity eventually becoming quadriplegic after 1 month. Imaging findings revealed a contrast-enhancing holocord neoplasm spanning from the cervical region to the conus medullaris and with extension to the lower medulla. The patient succumbed to severe pneumonia after 1 month of admission. An autopsy was done and the histopathologic findings were consistent with oligodendroglioma.
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spelling pubmed-60016862018-06-15 Holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature Cruz, Romulus Emmanuel H De Roxas, Ranhel C Sales-Callangan, Carmela Concepcion A Jamora, Roland Dominic G CNS Oncol Case Report Widespread primary spinal oligodendrogliomas are a rare variety of tumors that usually affect children. Currently, there are only two adult cases reported worldwide. We report the first case of primary holocord oligodendroglioma with intracranial extension in a young adult female. The patient presented with a 4-month history of fluctuating hemiparesis of the left upper extremity eventually becoming quadriplegic after 1 month. Imaging findings revealed a contrast-enhancing holocord neoplasm spanning from the cervical region to the conus medullaris and with extension to the lower medulla. The patient succumbed to severe pneumonia after 1 month of admission. An autopsy was done and the histopathologic findings were consistent with oligodendroglioma. Future Medicine Ltd 2018-02-02 /pmc/articles/PMC6001686/ /pubmed/29390865 http://dx.doi.org/10.2217/cns-2017-0012 Text en © 2018 Roland Dominic G Jamora This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Case Report
Cruz, Romulus Emmanuel H
De Roxas, Ranhel C
Sales-Callangan, Carmela Concepcion A
Jamora, Roland Dominic G
Holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature
title Holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature
title_full Holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature
title_fullStr Holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature
title_full_unstemmed Holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature
title_short Holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature
title_sort holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001686/
https://www.ncbi.nlm.nih.gov/pubmed/29390865
http://dx.doi.org/10.2217/cns-2017-0012
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