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Gliosarcoma in Young Adults: A Rare Variant of Glioblastoma
Gliosarcoma is a rare central nervous system (CNS) malignancy. It is characterized by classical biphasic histological pattern with both glial and sarcomatous components, often seen in fifth and sixth decade of life. They are generally located in the supratentorial region. Due to its rarity, exact tr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649997/ https://www.ncbi.nlm.nih.gov/pubmed/29147435 http://dx.doi.org/10.14740/wjon998w |
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author | Kakkar, Neha Kaur, Jaspreet Singh, Gunjesh Kumar Singh, Pragya Siraj, Fouzia Gupta, Ajay |
author_facet | Kakkar, Neha Kaur, Jaspreet Singh, Gunjesh Kumar Singh, Pragya Siraj, Fouzia Gupta, Ajay |
author_sort | Kakkar, Neha |
collection | PubMed |
description | Gliosarcoma is a rare central nervous system (CNS) malignancy. It is characterized by classical biphasic histological pattern with both glial and sarcomatous components, often seen in fifth and sixth decade of life. They are generally located in the supratentorial region. Due to its rarity, exact treatment recommendations are not available in literature. Since it is considered as a variant of glioblastoma multiforme (GBM), it is treated with surgery followed by adjuvant radiotherapy and temozolomide-based chemotherapy. We present a series of four cases of this rare malignancy that were treated at our institute. |
format | Online Article Text |
id | pubmed-5649997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56499972017-11-16 Gliosarcoma in Young Adults: A Rare Variant of Glioblastoma Kakkar, Neha Kaur, Jaspreet Singh, Gunjesh Kumar Singh, Pragya Siraj, Fouzia Gupta, Ajay World J Oncol Case Report Gliosarcoma is a rare central nervous system (CNS) malignancy. It is characterized by classical biphasic histological pattern with both glial and sarcomatous components, often seen in fifth and sixth decade of life. They are generally located in the supratentorial region. Due to its rarity, exact treatment recommendations are not available in literature. Since it is considered as a variant of glioblastoma multiforme (GBM), it is treated with surgery followed by adjuvant radiotherapy and temozolomide-based chemotherapy. We present a series of four cases of this rare malignancy that were treated at our institute. Elmer Press 2017-04 2017-05-04 /pmc/articles/PMC5649997/ /pubmed/29147435 http://dx.doi.org/10.14740/wjon998w Text en Copyright 2017, Kakkar et al. http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kakkar, Neha Kaur, Jaspreet Singh, Gunjesh Kumar Singh, Pragya Siraj, Fouzia Gupta, Ajay Gliosarcoma in Young Adults: A Rare Variant of Glioblastoma |
title | Gliosarcoma in Young Adults: A Rare Variant of Glioblastoma |
title_full | Gliosarcoma in Young Adults: A Rare Variant of Glioblastoma |
title_fullStr | Gliosarcoma in Young Adults: A Rare Variant of Glioblastoma |
title_full_unstemmed | Gliosarcoma in Young Adults: A Rare Variant of Glioblastoma |
title_short | Gliosarcoma in Young Adults: A Rare Variant of Glioblastoma |
title_sort | gliosarcoma in young adults: a rare variant of glioblastoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649997/ https://www.ncbi.nlm.nih.gov/pubmed/29147435 http://dx.doi.org/10.14740/wjon998w |
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