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From a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: Pitfalls of initial diagnosis on biopsy material, a case report

BACKGROUND: Ganglioglioma (GG) and dysembryoplastic neuroepithelial tumor (DNET) belong to the group of low-grade epilepsy-associated tumors (LEAT) and are the most prevalent tumor types found in patients undergoing epilepsy surgery. Histopathological differentiation between GG and DNET can be diffi...

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Autores principales: Slegers, Rutger J., Beckervordersandforth, Jan, Hoeben, Ann, Hoogland, Govert, Broen, Martijn P. G., Anten, Monique, Dings, Jim T. A., van den Ende, Piet, Henneman, Wouter J. P., Schijns, Olaf E. M. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888280/
https://www.ncbi.nlm.nih.gov/pubmed/35242409
http://dx.doi.org/10.25259/SNI_1153_2021
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author Slegers, Rutger J.
Beckervordersandforth, Jan
Hoeben, Ann
Hoogland, Govert
Broen, Martijn P. G.
Anten, Monique
Dings, Jim T. A.
van den Ende, Piet
Henneman, Wouter J. P.
Schijns, Olaf E. M. G.
author_facet Slegers, Rutger J.
Beckervordersandforth, Jan
Hoeben, Ann
Hoogland, Govert
Broen, Martijn P. G.
Anten, Monique
Dings, Jim T. A.
van den Ende, Piet
Henneman, Wouter J. P.
Schijns, Olaf E. M. G.
author_sort Slegers, Rutger J.
collection PubMed
description BACKGROUND: Ganglioglioma (GG) and dysembryoplastic neuroepithelial tumor (DNET) belong to the group of low-grade epilepsy-associated tumors (LEAT) and are the most prevalent tumor types found in patients undergoing epilepsy surgery. Histopathological differentiation between GG and DNET can be difficult on biopsies due to limited tumor tissue. CASE DESCRIPTION: Here, we present a rare case where a low-grade tumor was initially classified as DNET, based on biopsy findings and unfortunately dedifferentiated within 10 years into a glioblastoma multiforme. After gross total resection, the initial tumor was reclassified as GG. CONCLUSION: This case illustrates the diagnostic challenges of LEAT, especially on biopsy material. Therefore, we advocate to counsel for complete resection and histopathological diagnosis utilizing tumor markers to confirm the nature of the tumor and to advice type of follow-up and eventual concurrent treatment.
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spelling pubmed-88882802022-03-02 From a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: Pitfalls of initial diagnosis on biopsy material, a case report Slegers, Rutger J. Beckervordersandforth, Jan Hoeben, Ann Hoogland, Govert Broen, Martijn P. G. Anten, Monique Dings, Jim T. A. van den Ende, Piet Henneman, Wouter J. P. Schijns, Olaf E. M. G. Surg Neurol Int Case Report BACKGROUND: Ganglioglioma (GG) and dysembryoplastic neuroepithelial tumor (DNET) belong to the group of low-grade epilepsy-associated tumors (LEAT) and are the most prevalent tumor types found in patients undergoing epilepsy surgery. Histopathological differentiation between GG and DNET can be difficult on biopsies due to limited tumor tissue. CASE DESCRIPTION: Here, we present a rare case where a low-grade tumor was initially classified as DNET, based on biopsy findings and unfortunately dedifferentiated within 10 years into a glioblastoma multiforme. After gross total resection, the initial tumor was reclassified as GG. CONCLUSION: This case illustrates the diagnostic challenges of LEAT, especially on biopsy material. Therefore, we advocate to counsel for complete resection and histopathological diagnosis utilizing tumor markers to confirm the nature of the tumor and to advice type of follow-up and eventual concurrent treatment. Scientific Scholar 2022-02-11 /pmc/articles/PMC8888280/ /pubmed/35242409 http://dx.doi.org/10.25259/SNI_1153_2021 Text en Copyright: © 2022 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Slegers, Rutger J.
Beckervordersandforth, Jan
Hoeben, Ann
Hoogland, Govert
Broen, Martijn P. G.
Anten, Monique
Dings, Jim T. A.
van den Ende, Piet
Henneman, Wouter J. P.
Schijns, Olaf E. M. G.
From a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: Pitfalls of initial diagnosis on biopsy material, a case report
title From a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: Pitfalls of initial diagnosis on biopsy material, a case report
title_full From a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: Pitfalls of initial diagnosis on biopsy material, a case report
title_fullStr From a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: Pitfalls of initial diagnosis on biopsy material, a case report
title_full_unstemmed From a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: Pitfalls of initial diagnosis on biopsy material, a case report
title_short From a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: Pitfalls of initial diagnosis on biopsy material, a case report
title_sort from a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: pitfalls of initial diagnosis on biopsy material, a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888280/
https://www.ncbi.nlm.nih.gov/pubmed/35242409
http://dx.doi.org/10.25259/SNI_1153_2021
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