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A Case of Recurrent Supratentorial Extraventricular Anaplastic Ependymoma in Adult
Supratentorial extraventricular anaplastic ependymoma (SEAE) in adults is a relatively rare intracranial tumor. Because of the very low prevalence, only a few cases have been reported. According to a recent study, SEAE is associated with a poor prognosis and there is no definite consensus on optimal...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Brain Tumor Society; The Korean Society for Neuro-Oncology; The Korean Society for Pediatric Neuro-Oncology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504761/ https://www.ncbi.nlm.nih.gov/pubmed/31062531 http://dx.doi.org/10.14791/btrt.2019.7.e26 |
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author | Seo, Sung-Won Kang, Ho-Jun Lee, Min-Seok Suh, Sang-Jun Lee, Yoon-soo Lee, Jeong-Ho Kang, Dong-Gee |
author_facet | Seo, Sung-Won Kang, Ho-Jun Lee, Min-Seok Suh, Sang-Jun Lee, Yoon-soo Lee, Jeong-Ho Kang, Dong-Gee |
author_sort | Seo, Sung-Won |
collection | PubMed |
description | Supratentorial extraventricular anaplastic ependymoma (SEAE) in adults is a relatively rare intracranial tumor. Because of the very low prevalence, only a few cases have been reported. According to a recent study, SEAE is associated with a poor prognosis and there is no definite consensus on optimal treatment. We report a case of an adult SEAE patient who had no recurrence until seven years after a gross total resection (GTR) followed by conventional radiotherapy. A 42-year-old male had a persistent mild headache, left facial palsy, dysarthria, and left hemiparesis. Preoperative neuroimaging revealed an anaplastic astrocytoma or supratentorial ependymoma in the right frontal lobe. A GTR was performed, followed by adjuvant radiotherapy. Histologic and immunohistochemical results revealed anaplastic ependymoma. After seven years of initial therapy, a regular follow-up MRI showed a 3-cm-sized partially cystic mass in the same area as the initial tumor. The patient underwent a craniotomy, and a GTR was performed. Histopathologic examination revealed recurrence of the SEAE. External radiotherapy was performed. The patient has been stable without any disease progression or complications for 12 months since the surgery for recurrent SEAE. |
format | Online Article Text |
id | pubmed-6504761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Brain Tumor Society; The Korean Society for Neuro-Oncology; The Korean Society for Pediatric Neuro-Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-65047612019-05-20 A Case of Recurrent Supratentorial Extraventricular Anaplastic Ependymoma in Adult Seo, Sung-Won Kang, Ho-Jun Lee, Min-Seok Suh, Sang-Jun Lee, Yoon-soo Lee, Jeong-Ho Kang, Dong-Gee Brain Tumor Res Treat Case Report Supratentorial extraventricular anaplastic ependymoma (SEAE) in adults is a relatively rare intracranial tumor. Because of the very low prevalence, only a few cases have been reported. According to a recent study, SEAE is associated with a poor prognosis and there is no definite consensus on optimal treatment. We report a case of an adult SEAE patient who had no recurrence until seven years after a gross total resection (GTR) followed by conventional radiotherapy. A 42-year-old male had a persistent mild headache, left facial palsy, dysarthria, and left hemiparesis. Preoperative neuroimaging revealed an anaplastic astrocytoma or supratentorial ependymoma in the right frontal lobe. A GTR was performed, followed by adjuvant radiotherapy. Histologic and immunohistochemical results revealed anaplastic ependymoma. After seven years of initial therapy, a regular follow-up MRI showed a 3-cm-sized partially cystic mass in the same area as the initial tumor. The patient underwent a craniotomy, and a GTR was performed. Histopathologic examination revealed recurrence of the SEAE. External radiotherapy was performed. The patient has been stable without any disease progression or complications for 12 months since the surgery for recurrent SEAE. The Korean Brain Tumor Society; The Korean Society for Neuro-Oncology; The Korean Society for Pediatric Neuro-Oncology 2019-04 2019-04-30 /pmc/articles/PMC6504761/ /pubmed/31062531 http://dx.doi.org/10.14791/btrt.2019.7.e26 Text en Copyright © 2019 The Korean Brain Tumor Society, The Korean Society for Neuro-Oncology, and The Korean Society for Pediatric Neuro-Oncology http://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/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Seo, Sung-Won Kang, Ho-Jun Lee, Min-Seok Suh, Sang-Jun Lee, Yoon-soo Lee, Jeong-Ho Kang, Dong-Gee A Case of Recurrent Supratentorial Extraventricular Anaplastic Ependymoma in Adult |
title | A Case of Recurrent Supratentorial Extraventricular Anaplastic Ependymoma in Adult |
title_full | A Case of Recurrent Supratentorial Extraventricular Anaplastic Ependymoma in Adult |
title_fullStr | A Case of Recurrent Supratentorial Extraventricular Anaplastic Ependymoma in Adult |
title_full_unstemmed | A Case of Recurrent Supratentorial Extraventricular Anaplastic Ependymoma in Adult |
title_short | A Case of Recurrent Supratentorial Extraventricular Anaplastic Ependymoma in Adult |
title_sort | case of recurrent supratentorial extraventricular anaplastic ependymoma in adult |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504761/ https://www.ncbi.nlm.nih.gov/pubmed/31062531 http://dx.doi.org/10.14791/btrt.2019.7.e26 |
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