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Primary pediatric cerebellar gliosarcoma

BACKGROUND: Primary gliosarcomas of the central nervous are rare and very few have been reported in the infratentorial compartment. Here, we describe such a lesion in a 12-year-old male. CASE DESCRIPTION: A 12-year-old male presented with headache, ataxia, and vomiting. When Magnetic resonance studi...

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Autores principales: Bukhari, Syed Sarmad, Junaid, Muhammad, Afzal, Ali, Kulsoom, Anisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265428/
https://www.ncbi.nlm.nih.gov/pubmed/32494375
http://dx.doi.org/10.25259/SNI_274_2019
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author Bukhari, Syed Sarmad
Junaid, Muhammad
Afzal, Ali
Kulsoom, Anisa
author_facet Bukhari, Syed Sarmad
Junaid, Muhammad
Afzal, Ali
Kulsoom, Anisa
author_sort Bukhari, Syed Sarmad
collection PubMed
description BACKGROUND: Primary gliosarcomas of the central nervous are rare and very few have been reported in the infratentorial compartment. Here, we describe such a lesion in a 12-year-old male. CASE DESCRIPTION: A 12-year-old male presented with headache, ataxia, and vomiting. When Magnetic resonance studies documented a posterior fossa lesion, he underwent placement of a right ventriculoperitoneal shunt followed by a suboccipital craniectomy. The lesion proved to be a primary gliosarcoma. Unfortunately, it recurred 2 years later and required repeated resection. CONCLUSION: Here, we reviewed the rare case of a 12-year-old male requiring shunt placement and suboccipital craniectomy for a primary gliosarcoma that recurred 2 years later.
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spelling pubmed-72654282020-06-02 Primary pediatric cerebellar gliosarcoma Bukhari, Syed Sarmad Junaid, Muhammad Afzal, Ali Kulsoom, Anisa Surg Neurol Int Case Report BACKGROUND: Primary gliosarcomas of the central nervous are rare and very few have been reported in the infratentorial compartment. Here, we describe such a lesion in a 12-year-old male. CASE DESCRIPTION: A 12-year-old male presented with headache, ataxia, and vomiting. When Magnetic resonance studies documented a posterior fossa lesion, he underwent placement of a right ventriculoperitoneal shunt followed by a suboccipital craniectomy. The lesion proved to be a primary gliosarcoma. Unfortunately, it recurred 2 years later and required repeated resection. CONCLUSION: Here, we reviewed the rare case of a 12-year-old male requiring shunt placement and suboccipital craniectomy for a primary gliosarcoma that recurred 2 years later. Scientific Scholar 2020-05-09 /pmc/articles/PMC7265428/ /pubmed/32494375 http://dx.doi.org/10.25259/SNI_274_2019 Text en Copyright: © 2020 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Bukhari, Syed Sarmad
Junaid, Muhammad
Afzal, Ali
Kulsoom, Anisa
Primary pediatric cerebellar gliosarcoma
title Primary pediatric cerebellar gliosarcoma
title_full Primary pediatric cerebellar gliosarcoma
title_fullStr Primary pediatric cerebellar gliosarcoma
title_full_unstemmed Primary pediatric cerebellar gliosarcoma
title_short Primary pediatric cerebellar gliosarcoma
title_sort primary pediatric cerebellar gliosarcoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265428/
https://www.ncbi.nlm.nih.gov/pubmed/32494375
http://dx.doi.org/10.25259/SNI_274_2019
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