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A novel histopathological grading system for ganglioglioma

Gangliogliomas are central nervous system tumors located in the temporal lobe of young patients, frequently associated with epilepsy. In this paper, we propose a grading system based solely on histopathological criteria. We reevaluated all cases of ganglioglioma, atypical ganglioglioma, and anaplast...

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Autores principales: Lisievici, Antonia Carmen, Pasov, Diana, Georgescu, Tiberiu-Augustin, Lisievici, Mihai Gheorghe, Sajin, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Carol Davila University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169146/
https://www.ncbi.nlm.nih.gov/pubmed/34104239
http://dx.doi.org/10.25122/jml-2021-0054
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author Lisievici, Antonia Carmen
Pasov, Diana
Georgescu, Tiberiu-Augustin
Lisievici, Mihai Gheorghe
Sajin, Maria
author_facet Lisievici, Antonia Carmen
Pasov, Diana
Georgescu, Tiberiu-Augustin
Lisievici, Mihai Gheorghe
Sajin, Maria
author_sort Lisievici, Antonia Carmen
collection PubMed
description Gangliogliomas are central nervous system tumors located in the temporal lobe of young patients, frequently associated with epilepsy. In this paper, we propose a grading system based solely on histopathological criteria. We reevaluated all cases of ganglioglioma, atypical ganglioglioma, and anaplastic ganglioglioma diagnosed between 2011 and 2020 in the Pathology Department of the Emergency Clinical Hospital Bagdasar-Arseni, based on the type of glial mitoses, the number of neuronal and glial mitoses, presence of necrosis, microvascular proliferation, eosinophilic granular bodies, hypercellularity, presence and disposition of inflammatory infiltrate and atypical pleomorphism. Based on the proposed grading system, a score of 0–4 corresponded to a benign ganglioglioma, 5–9 to an atypical ganglioglioma, and 10–18 to an anaplastic ganglioglioma. The survival rates were 90% for benign ganglioglioma, 71.43% for atypical ganglioglioma, and 62.54% for anaplastic ganglioglioma. One case of benign ganglioglioma underwent a malignant transformation into anaplastic ganglioglioma, and recurrences were noticed in 28.57% of atypical ganglioglioma cases and 30.7% of all anaplastic gangliogliomas. The presence of rare glial mitoses and hypercellularity was correlated with mortality in cases of atypical ganglioglioma. We believe this histopathological scoring system could be used as a three-tier system to identify atypical ganglioglioma cases that are bound to have an aggressive course of evolution and require close follow-up. The other option would be to convert it to a two-tier grading system that can separate low-grade gangliogliomas from high-grade ones. The latter category can encompass both atypical and anaplastic ganglioglioma due to the high mortality of both entities.
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spelling pubmed-81691462021-06-07 A novel histopathological grading system for ganglioglioma Lisievici, Antonia Carmen Pasov, Diana Georgescu, Tiberiu-Augustin Lisievici, Mihai Gheorghe Sajin, Maria J Med Life Original Article Gangliogliomas are central nervous system tumors located in the temporal lobe of young patients, frequently associated with epilepsy. In this paper, we propose a grading system based solely on histopathological criteria. We reevaluated all cases of ganglioglioma, atypical ganglioglioma, and anaplastic ganglioglioma diagnosed between 2011 and 2020 in the Pathology Department of the Emergency Clinical Hospital Bagdasar-Arseni, based on the type of glial mitoses, the number of neuronal and glial mitoses, presence of necrosis, microvascular proliferation, eosinophilic granular bodies, hypercellularity, presence and disposition of inflammatory infiltrate and atypical pleomorphism. Based on the proposed grading system, a score of 0–4 corresponded to a benign ganglioglioma, 5–9 to an atypical ganglioglioma, and 10–18 to an anaplastic ganglioglioma. The survival rates were 90% for benign ganglioglioma, 71.43% for atypical ganglioglioma, and 62.54% for anaplastic ganglioglioma. One case of benign ganglioglioma underwent a malignant transformation into anaplastic ganglioglioma, and recurrences were noticed in 28.57% of atypical ganglioglioma cases and 30.7% of all anaplastic gangliogliomas. The presence of rare glial mitoses and hypercellularity was correlated with mortality in cases of atypical ganglioglioma. We believe this histopathological scoring system could be used as a three-tier system to identify atypical ganglioglioma cases that are bound to have an aggressive course of evolution and require close follow-up. The other option would be to convert it to a two-tier grading system that can separate low-grade gangliogliomas from high-grade ones. The latter category can encompass both atypical and anaplastic ganglioglioma due to the high mortality of both entities. Carol Davila University Press 2021 /pmc/articles/PMC8169146/ /pubmed/34104239 http://dx.doi.org/10.25122/jml-2021-0054 Text en ©2021 JOURNAL of MEDICINE and LIFE https://creativecommons.org/licenses/by/3.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Original Article
Lisievici, Antonia Carmen
Pasov, Diana
Georgescu, Tiberiu-Augustin
Lisievici, Mihai Gheorghe
Sajin, Maria
A novel histopathological grading system for ganglioglioma
title A novel histopathological grading system for ganglioglioma
title_full A novel histopathological grading system for ganglioglioma
title_fullStr A novel histopathological grading system for ganglioglioma
title_full_unstemmed A novel histopathological grading system for ganglioglioma
title_short A novel histopathological grading system for ganglioglioma
title_sort novel histopathological grading system for ganglioglioma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169146/
https://www.ncbi.nlm.nih.gov/pubmed/34104239
http://dx.doi.org/10.25122/jml-2021-0054
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