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A Rare Case of Dysembryoplastic Neuroepithelial Tumor

We present a rare case of dysembryoplastic neuroepithelial tumor, a rare benign glioneuronal tumor of the central nervous system. It generally occurs in the supratentorial region and the temporal cerebral cortex in children and young adults. The most common presentation is epilepsy. The supratentori...

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Autores principales: Guduru, Harsha, Shen, Jun K., Lokannavar, Harish S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515966/
https://www.ncbi.nlm.nih.gov/pubmed/23230542
http://dx.doi.org/10.4103/2156-7514.102057
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author Guduru, Harsha
Shen, Jun K.
Lokannavar, Harish S.
author_facet Guduru, Harsha
Shen, Jun K.
Lokannavar, Harish S.
author_sort Guduru, Harsha
collection PubMed
description We present a rare case of dysembryoplastic neuroepithelial tumor, a rare benign glioneuronal tumor of the central nervous system. It generally occurs in the supratentorial region and the temporal cerebral cortex in children and young adults. The most common presentation is epilepsy. The supratentorial tumor without any signs of mass effect or peritumoral edema is the conventionally accepted diagnostic criteria. In this case of a 19-year-old male with intractable epilepsy, atypical features such as the location of the tumor and the presence of mass effect and peritumoral edema made imaging diagnosis difficult. Diagnosis was confirmed through histopathology. Due to its recent discovery and relatively rare occurrence it is important for radiologists to recognize this disease entity.
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spelling pubmed-35159662012-12-10 A Rare Case of Dysembryoplastic Neuroepithelial Tumor Guduru, Harsha Shen, Jun K. Lokannavar, Harish S. J Clin Imaging Sci Case Report We present a rare case of dysembryoplastic neuroepithelial tumor, a rare benign glioneuronal tumor of the central nervous system. It generally occurs in the supratentorial region and the temporal cerebral cortex in children and young adults. The most common presentation is epilepsy. The supratentorial tumor without any signs of mass effect or peritumoral edema is the conventionally accepted diagnostic criteria. In this case of a 19-year-old male with intractable epilepsy, atypical features such as the location of the tumor and the presence of mass effect and peritumoral edema made imaging diagnosis difficult. Diagnosis was confirmed through histopathology. Due to its recent discovery and relatively rare occurrence it is important for radiologists to recognize this disease entity. Medknow Publications & Media Pvt Ltd 2012-10-06 /pmc/articles/PMC3515966/ /pubmed/23230542 http://dx.doi.org/10.4103/2156-7514.102057 Text en Copyright: © 2012 Guduru H 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
Guduru, Harsha
Shen, Jun K.
Lokannavar, Harish S.
A Rare Case of Dysembryoplastic Neuroepithelial Tumor
title A Rare Case of Dysembryoplastic Neuroepithelial Tumor
title_full A Rare Case of Dysembryoplastic Neuroepithelial Tumor
title_fullStr A Rare Case of Dysembryoplastic Neuroepithelial Tumor
title_full_unstemmed A Rare Case of Dysembryoplastic Neuroepithelial Tumor
title_short A Rare Case of Dysembryoplastic Neuroepithelial Tumor
title_sort rare case of dysembryoplastic neuroepithelial tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515966/
https://www.ncbi.nlm.nih.gov/pubmed/23230542
http://dx.doi.org/10.4103/2156-7514.102057
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