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Mediastinal Anaplastic Ependymoma

Ependymomas arise from ependymal cells and can grow at any site in the central nervous system (CNS), as well as in some locations outside of the CNS. The latter is rare, contributing to the frequent misdiagnoses of such cases. Herein, we present the case of a 54-year-old man with a history of lower...

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Autores principales: Fauziah, Dyah, Parengkuan, Irene Lingkan, Jiwangga, Dhihintia, Raharjo, Paulus, Basuki, Mudjiani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Thoracic and Cardiovascular Surgery 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8181701/
https://www.ncbi.nlm.nih.gov/pubmed/33767021
http://dx.doi.org/10.5090/jcs.20.094
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author Fauziah, Dyah
Parengkuan, Irene Lingkan
Jiwangga, Dhihintia
Raharjo, Paulus
Basuki, Mudjiani
author_facet Fauziah, Dyah
Parengkuan, Irene Lingkan
Jiwangga, Dhihintia
Raharjo, Paulus
Basuki, Mudjiani
author_sort Fauziah, Dyah
collection PubMed
description Ependymomas arise from ependymal cells and can grow at any site in the central nervous system (CNS), as well as in some locations outside of the CNS. The latter is rare, contributing to the frequent misdiagnoses of such cases. Herein, we present the case of a 54-year-old man with a history of lower limb weakness and numbness. Magnetic resonance imaging revealed an extradural, heterogeneously enhanced solid lesion with a regular and well-defined border in the posterior mediastinum. A post-resection histopathological examination revealed tumor-forming perivascular pseudo-rosettes that showed immunoreactivity against glial fibrillary acidic protein, epithelial membrane antigen, and vimentin, as well as a high Ki-67 labeling index. Based on pathological features, a diagnosis of anaplastic ependymoma was established.
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spelling pubmed-81817012021-06-16 Mediastinal Anaplastic Ependymoma Fauziah, Dyah Parengkuan, Irene Lingkan Jiwangga, Dhihintia Raharjo, Paulus Basuki, Mudjiani J Chest Surg Case Report Ependymomas arise from ependymal cells and can grow at any site in the central nervous system (CNS), as well as in some locations outside of the CNS. The latter is rare, contributing to the frequent misdiagnoses of such cases. Herein, we present the case of a 54-year-old man with a history of lower limb weakness and numbness. Magnetic resonance imaging revealed an extradural, heterogeneously enhanced solid lesion with a regular and well-defined border in the posterior mediastinum. A post-resection histopathological examination revealed tumor-forming perivascular pseudo-rosettes that showed immunoreactivity against glial fibrillary acidic protein, epithelial membrane antigen, and vimentin, as well as a high Ki-67 labeling index. Based on pathological features, a diagnosis of anaplastic ependymoma was established. The Korean Society for Thoracic and Cardiovascular Surgery 2021-06-05 2021-06-05 /pmc/articles/PMC8181701/ /pubmed/33767021 http://dx.doi.org/10.5090/jcs.20.094 Text en Copyright © The Korean Society for Thoracic and Cardiovascular Surgery. 2021. All right reserved. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Fauziah, Dyah
Parengkuan, Irene Lingkan
Jiwangga, Dhihintia
Raharjo, Paulus
Basuki, Mudjiani
Mediastinal Anaplastic Ependymoma
title Mediastinal Anaplastic Ependymoma
title_full Mediastinal Anaplastic Ependymoma
title_fullStr Mediastinal Anaplastic Ependymoma
title_full_unstemmed Mediastinal Anaplastic Ependymoma
title_short Mediastinal Anaplastic Ependymoma
title_sort mediastinal anaplastic ependymoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8181701/
https://www.ncbi.nlm.nih.gov/pubmed/33767021
http://dx.doi.org/10.5090/jcs.20.094
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