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MRI Findings of Desmoplastic Infantile Ganglioglioma: A Case Report and Analysis

Desmoplastic infantile gangliogliomas (DIG) are rare intracranial tumors that predominantly affect children. They are characterized by a mixture of glial and neuronal components interspersed with abundant fibrous stroma and are typically located on the surface of the cerebral hemispheres. In this ca...

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Autores principales: Dias, Diego Jordão L, Dias, Amanda Selvátici dos S, Camargo, Marcos V, Lederman, Henrique M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506886/
https://www.ncbi.nlm.nih.gov/pubmed/37727160
http://dx.doi.org/10.7759/cureus.43770
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author Dias, Diego Jordão L
Dias, Amanda Selvátici dos S
Camargo, Marcos V
Lederman, Henrique M
author_facet Dias, Diego Jordão L
Dias, Amanda Selvátici dos S
Camargo, Marcos V
Lederman, Henrique M
author_sort Dias, Diego Jordão L
collection PubMed
description Desmoplastic infantile gangliogliomas (DIG) are rare intracranial tumors that predominantly affect children. They are characterized by a mixture of glial and neuronal components interspersed with abundant fibrous stroma and are typically located on the surface of the cerebral hemispheres. In this case report, we present a seven-year-old male child with a late presentation of DIG, which is typically diagnosed between zero and 60 months of age. We discuss the MRI findings, clinical symptoms, and differential diagnosis of DIG in patients with this central nervous system tumor.
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spelling pubmed-105068862023-09-19 MRI Findings of Desmoplastic Infantile Ganglioglioma: A Case Report and Analysis Dias, Diego Jordão L Dias, Amanda Selvátici dos S Camargo, Marcos V Lederman, Henrique M Cureus Pediatric Surgery Desmoplastic infantile gangliogliomas (DIG) are rare intracranial tumors that predominantly affect children. They are characterized by a mixture of glial and neuronal components interspersed with abundant fibrous stroma and are typically located on the surface of the cerebral hemispheres. In this case report, we present a seven-year-old male child with a late presentation of DIG, which is typically diagnosed between zero and 60 months of age. We discuss the MRI findings, clinical symptoms, and differential diagnosis of DIG in patients with this central nervous system tumor. Cureus 2023-08-19 /pmc/articles/PMC10506886/ /pubmed/37727160 http://dx.doi.org/10.7759/cureus.43770 Text en Copyright © 2023, Dias et al. https://creativecommons.org/licenses/by/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 Pediatric Surgery
Dias, Diego Jordão L
Dias, Amanda Selvátici dos S
Camargo, Marcos V
Lederman, Henrique M
MRI Findings of Desmoplastic Infantile Ganglioglioma: A Case Report and Analysis
title MRI Findings of Desmoplastic Infantile Ganglioglioma: A Case Report and Analysis
title_full MRI Findings of Desmoplastic Infantile Ganglioglioma: A Case Report and Analysis
title_fullStr MRI Findings of Desmoplastic Infantile Ganglioglioma: A Case Report and Analysis
title_full_unstemmed MRI Findings of Desmoplastic Infantile Ganglioglioma: A Case Report and Analysis
title_short MRI Findings of Desmoplastic Infantile Ganglioglioma: A Case Report and Analysis
title_sort mri findings of desmoplastic infantile ganglioglioma: a case report and analysis
topic Pediatric Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506886/
https://www.ncbi.nlm.nih.gov/pubmed/37727160
http://dx.doi.org/10.7759/cureus.43770
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