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Thoracic intramedullary schwannoma: A case report and review of literature

Intramedullary schwannomas are rare spinal cord tumors. Most of these tumors have been reported as a single lesion in the spinal cord. Up until today approximately 50 cases of intramedullary shwannomas not related to neurofibromatosis have been described. We describe a rare case of thoracic intramed...

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Autores principales: Nayak, Raghavendra, Chaudhuri, Anupkumar, Chattopadhyay, Aniruddha, Ghosh, S. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421952/
https://www.ncbi.nlm.nih.gov/pubmed/25972946
http://dx.doi.org/10.4103/1793-5482.145155
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author Nayak, Raghavendra
Chaudhuri, Anupkumar
Chattopadhyay, Aniruddha
Ghosh, S. N.
author_facet Nayak, Raghavendra
Chaudhuri, Anupkumar
Chattopadhyay, Aniruddha
Ghosh, S. N.
author_sort Nayak, Raghavendra
collection PubMed
description Intramedullary schwannomas are rare spinal cord tumors. Most of these tumors have been reported as a single lesion in the spinal cord. Up until today approximately 50 cases of intramedullary shwannomas not related to neurofibromatosis have been described. We describe a rare case of thoracic intramedullary tumour in a 28 year old male patient who presented with progressive weakness of both the lower limbs and decreased sensation below D2 dermatomal level. Magnetic resonance imaging revealed an intramedullary lesion from D1 toD7. D1 to D7 laminoplasty and near total excision of the mass done. Total removal was difficult because of the infiltrative nature of the tumour. Histopathological report confirmed the diagnosis of the schwannoma. Possible site of origin and pathogenesis of intramedullary tumour have been discussed.
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spelling pubmed-44219522015-05-13 Thoracic intramedullary schwannoma: A case report and review of literature Nayak, Raghavendra Chaudhuri, Anupkumar Chattopadhyay, Aniruddha Ghosh, S. N. Asian J Neurosurg Case Report Intramedullary schwannomas are rare spinal cord tumors. Most of these tumors have been reported as a single lesion in the spinal cord. Up until today approximately 50 cases of intramedullary shwannomas not related to neurofibromatosis have been described. We describe a rare case of thoracic intramedullary tumour in a 28 year old male patient who presented with progressive weakness of both the lower limbs and decreased sensation below D2 dermatomal level. Magnetic resonance imaging revealed an intramedullary lesion from D1 toD7. D1 to D7 laminoplasty and near total excision of the mass done. Total removal was difficult because of the infiltrative nature of the tumour. Histopathological report confirmed the diagnosis of the schwannoma. Possible site of origin and pathogenesis of intramedullary tumour have been discussed. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4421952/ /pubmed/25972946 http://dx.doi.org/10.4103/1793-5482.145155 Text en Copyright: © Asian Journal of Neurosurgery 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nayak, Raghavendra
Chaudhuri, Anupkumar
Chattopadhyay, Aniruddha
Ghosh, S. N.
Thoracic intramedullary schwannoma: A case report and review of literature
title Thoracic intramedullary schwannoma: A case report and review of literature
title_full Thoracic intramedullary schwannoma: A case report and review of literature
title_fullStr Thoracic intramedullary schwannoma: A case report and review of literature
title_full_unstemmed Thoracic intramedullary schwannoma: A case report and review of literature
title_short Thoracic intramedullary schwannoma: A case report and review of literature
title_sort thoracic intramedullary schwannoma: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421952/
https://www.ncbi.nlm.nih.gov/pubmed/25972946
http://dx.doi.org/10.4103/1793-5482.145155
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