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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...

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Detalles Bibliográficos
Autores principales: Kakkar, Neha, Kaur, Jaspreet, Singh, Gunjesh Kumar, Singh, Pragya, Siraj, Fouzia, Gupta, Ajay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2017
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.
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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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