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Rapidly Enlarging Pediatric Cortical Ependymoma

We report a 10-year-old boy with supratentorial cortical ependymoma that rapidly grew in the course of 3 years. He suffered generalized seizures when he was 5 years old; MRI showed a small cortical lesion in the right postcentral gyrus. MRI performed 2 years later revealed no changes. For the next 3...

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Autores principales: Yamasaki, Kouji, Yokogami, Kiyotaka, Yamashita, Shinji, Takeshima, Hideo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Neurosurgical Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502251/
https://www.ncbi.nlm.nih.gov/pubmed/26180622
http://dx.doi.org/10.3340/jkns.2015.57.6.487
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author Yamasaki, Kouji
Yokogami, Kiyotaka
Yamashita, Shinji
Takeshima, Hideo
author_facet Yamasaki, Kouji
Yokogami, Kiyotaka
Yamashita, Shinji
Takeshima, Hideo
author_sort Yamasaki, Kouji
collection PubMed
description We report a 10-year-old boy with supratentorial cortical ependymoma that rapidly grew in the course of 3 years. He suffered generalized seizures when he was 5 years old; MRI showed a small cortical lesion in the right postcentral gyrus. MRI performed 2 years later revealed no changes. For the next 3 years he was free of seizures. However, at the age of 10 he again suffered generalized seizures and MRI disclosed a large parietal tumor. It was resected totally and he remains free of neurological deficits. The histopathological diagnosis was ependymoma. Pediatric supratentorial cortical ependymomas are extremely rare. We recommend including cortical ependymoma as a differential diagnosis in pediatric patients with cortical mass lesions presenting with seizures and careful follow-up even in the absence of symptoms because these tumors may progress.
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spelling pubmed-45022512015-07-15 Rapidly Enlarging Pediatric Cortical Ependymoma Yamasaki, Kouji Yokogami, Kiyotaka Yamashita, Shinji Takeshima, Hideo J Korean Neurosurg Soc Case Report We report a 10-year-old boy with supratentorial cortical ependymoma that rapidly grew in the course of 3 years. He suffered generalized seizures when he was 5 years old; MRI showed a small cortical lesion in the right postcentral gyrus. MRI performed 2 years later revealed no changes. For the next 3 years he was free of seizures. However, at the age of 10 he again suffered generalized seizures and MRI disclosed a large parietal tumor. It was resected totally and he remains free of neurological deficits. The histopathological diagnosis was ependymoma. Pediatric supratentorial cortical ependymomas are extremely rare. We recommend including cortical ependymoma as a differential diagnosis in pediatric patients with cortical mass lesions presenting with seizures and careful follow-up even in the absence of symptoms because these tumors may progress. The Korean Neurosurgical Society 2015-06 2015-06-30 /pmc/articles/PMC4502251/ /pubmed/26180622 http://dx.doi.org/10.3340/jkns.2015.57.6.487 Text en Copyright © 2015 The Korean Neurosurgical Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Yamasaki, Kouji
Yokogami, Kiyotaka
Yamashita, Shinji
Takeshima, Hideo
Rapidly Enlarging Pediatric Cortical Ependymoma
title Rapidly Enlarging Pediatric Cortical Ependymoma
title_full Rapidly Enlarging Pediatric Cortical Ependymoma
title_fullStr Rapidly Enlarging Pediatric Cortical Ependymoma
title_full_unstemmed Rapidly Enlarging Pediatric Cortical Ependymoma
title_short Rapidly Enlarging Pediatric Cortical Ependymoma
title_sort rapidly enlarging pediatric cortical ependymoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502251/
https://www.ncbi.nlm.nih.gov/pubmed/26180622
http://dx.doi.org/10.3340/jkns.2015.57.6.487
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