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Intracranial periventricular supratentorial intraparenchymal schwannoma

BACKGROUND: Intraparenchymal schwannomas in the central nervous system are very rare. Because most of these are benign, complete excision is the treatment of choice. Further, their radiological findings are difficult to differentiate from glioma. Because Schwann cells are not indigenous to cerebral...

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Autores principales: Gupta, Anshul, Sharma, Divyam, Dhillon, Gurupal Singh, Chhabra, Satnam Singh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234275/
https://www.ncbi.nlm.nih.gov/pubmed/28144475
http://dx.doi.org/10.4103/2152-7806.195584
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author Gupta, Anshul
Sharma, Divyam
Dhillon, Gurupal Singh
Chhabra, Satnam Singh
author_facet Gupta, Anshul
Sharma, Divyam
Dhillon, Gurupal Singh
Chhabra, Satnam Singh
author_sort Gupta, Anshul
collection PubMed
description BACKGROUND: Intraparenchymal schwannomas in the central nervous system are very rare. Because most of these are benign, complete excision is the treatment of choice. Further, their radiological findings are difficult to differentiate from glioma. Because Schwann cells are not indigenous to cerebral parenchyma, a lot of speculation has been attached to their origin. CASE DESCRIPTION: We report one such rare case of a 17-year-old male who presented to us with a history of headache and vomiting. Neuroradiological findings were suggestive of left temporoparietal solid cystic lesion with enhancement of solid component, suggestive of high grade glioma. CONCLUSION: Intraoperative impression was that of a low-grade glioma but histopathological features were represented as schwannoma.
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spelling pubmed-52342752017-01-31 Intracranial periventricular supratentorial intraparenchymal schwannoma Gupta, Anshul Sharma, Divyam Dhillon, Gurupal Singh Chhabra, Satnam Singh Surg Neurol Int Case Report BACKGROUND: Intraparenchymal schwannomas in the central nervous system are very rare. Because most of these are benign, complete excision is the treatment of choice. Further, their radiological findings are difficult to differentiate from glioma. Because Schwann cells are not indigenous to cerebral parenchyma, a lot of speculation has been attached to their origin. CASE DESCRIPTION: We report one such rare case of a 17-year-old male who presented to us with a history of headache and vomiting. Neuroradiological findings were suggestive of left temporoparietal solid cystic lesion with enhancement of solid component, suggestive of high grade glioma. CONCLUSION: Intraoperative impression was that of a low-grade glioma but histopathological features were represented as schwannoma. Medknow Publications & Media Pvt Ltd 2016-12-12 /pmc/articles/PMC5234275/ /pubmed/28144475 http://dx.doi.org/10.4103/2152-7806.195584 Text en Copyright: © 2016 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 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
Gupta, Anshul
Sharma, Divyam
Dhillon, Gurupal Singh
Chhabra, Satnam Singh
Intracranial periventricular supratentorial intraparenchymal schwannoma
title Intracranial periventricular supratentorial intraparenchymal schwannoma
title_full Intracranial periventricular supratentorial intraparenchymal schwannoma
title_fullStr Intracranial periventricular supratentorial intraparenchymal schwannoma
title_full_unstemmed Intracranial periventricular supratentorial intraparenchymal schwannoma
title_short Intracranial periventricular supratentorial intraparenchymal schwannoma
title_sort intracranial periventricular supratentorial intraparenchymal schwannoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234275/
https://www.ncbi.nlm.nih.gov/pubmed/28144475
http://dx.doi.org/10.4103/2152-7806.195584
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