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Primary intraosseous malignant peripheral nerve sheath tumor of spine with a giant paraspinal and retrospinal subcutaneous extension

BACKGROUND: According to World Health Organization (WHO) classification of tumors, malignant peripheral nerve sheath tumors (MPNST) encompass the tumors, which were previously termed as malignant schwannoma, neurogenic sarcoma, and neurofibrosarcoma. These are rare tumors constituting only 5% of all...

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Autores principales: Patnaik, Ashis, Mishra, Sudhansu Sekhar, Senapati, Satya Bhushan, Patra, Sunil Kalpalata, Tripathy, Kalpalata, Burma, Subrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551491/
https://www.ncbi.nlm.nih.gov/pubmed/23372973
http://dx.doi.org/10.4103/2152-7806.105096
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author Patnaik, Ashis
Mishra, Sudhansu Sekhar
Senapati, Satya Bhushan
Patra, Sunil Kalpalata
Tripathy, Kalpalata
Burma, Subrat
author_facet Patnaik, Ashis
Mishra, Sudhansu Sekhar
Senapati, Satya Bhushan
Patra, Sunil Kalpalata
Tripathy, Kalpalata
Burma, Subrat
author_sort Patnaik, Ashis
collection PubMed
description BACKGROUND: According to World Health Organization (WHO) classification of tumors, malignant peripheral nerve sheath tumors (MPNST) encompass the tumors, which were previously termed as malignant schwannoma, neurogenic sarcoma, and neurofibrosarcoma. These are rare tumors constituting only 5% of all malignant soft tissue tumors. As per their name, they arise from the malignant proliferation of cells forming sheath of a nerve root. They cause spinal cord compression, secondary changes in the surrounding bone with variable amount of tumor tissue going into the paraspinal space. However, purely intraosseous origin of the MPNST with no visible connection with a nerve root or dura is rare and few cases have been described in the literature. CASE DESCRIPTION: We present a primary intraosseous MPNST arising from the body of a thoracic spine with a minimal intraspinal component. However, there was a huge tumor part occupying the paraspinal and retrospinal region. The latter component was so large that it extended to lie just beneath the skin. The intraspinal component was confined to only one level. The giant extraspinal part was spanning multiple corresponding spinal level. We could not find such presentation in the literature. CONCLUSION: Gross total removal (GTR) followed by adjuvant chemo-radiotherapy is the optimal treatment for MPNST of spine. In case of multiple laminectomy or gross spinal instability, spinal instrumentation makes the treatment protocol complete.
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spelling pubmed-35514912013-01-31 Primary intraosseous malignant peripheral nerve sheath tumor of spine with a giant paraspinal and retrospinal subcutaneous extension Patnaik, Ashis Mishra, Sudhansu Sekhar Senapati, Satya Bhushan Patra, Sunil Kalpalata Tripathy, Kalpalata Burma, Subrat Surg Neurol Int Case Report BACKGROUND: According to World Health Organization (WHO) classification of tumors, malignant peripheral nerve sheath tumors (MPNST) encompass the tumors, which were previously termed as malignant schwannoma, neurogenic sarcoma, and neurofibrosarcoma. These are rare tumors constituting only 5% of all malignant soft tissue tumors. As per their name, they arise from the malignant proliferation of cells forming sheath of a nerve root. They cause spinal cord compression, secondary changes in the surrounding bone with variable amount of tumor tissue going into the paraspinal space. However, purely intraosseous origin of the MPNST with no visible connection with a nerve root or dura is rare and few cases have been described in the literature. CASE DESCRIPTION: We present a primary intraosseous MPNST arising from the body of a thoracic spine with a minimal intraspinal component. However, there was a huge tumor part occupying the paraspinal and retrospinal region. The latter component was so large that it extended to lie just beneath the skin. The intraspinal component was confined to only one level. The giant extraspinal part was spanning multiple corresponding spinal level. We could not find such presentation in the literature. CONCLUSION: Gross total removal (GTR) followed by adjuvant chemo-radiotherapy is the optimal treatment for MPNST of spine. In case of multiple laminectomy or gross spinal instability, spinal instrumentation makes the treatment protocol complete. Medknow Publications & Media Pvt Ltd 2012-12-26 /pmc/articles/PMC3551491/ /pubmed/23372973 http://dx.doi.org/10.4103/2152-7806.105096 Text en Copyright: © 2012 Patnaik A http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Patnaik, Ashis
Mishra, Sudhansu Sekhar
Senapati, Satya Bhushan
Patra, Sunil Kalpalata
Tripathy, Kalpalata
Burma, Subrat
Primary intraosseous malignant peripheral nerve sheath tumor of spine with a giant paraspinal and retrospinal subcutaneous extension
title Primary intraosseous malignant peripheral nerve sheath tumor of spine with a giant paraspinal and retrospinal subcutaneous extension
title_full Primary intraosseous malignant peripheral nerve sheath tumor of spine with a giant paraspinal and retrospinal subcutaneous extension
title_fullStr Primary intraosseous malignant peripheral nerve sheath tumor of spine with a giant paraspinal and retrospinal subcutaneous extension
title_full_unstemmed Primary intraosseous malignant peripheral nerve sheath tumor of spine with a giant paraspinal and retrospinal subcutaneous extension
title_short Primary intraosseous malignant peripheral nerve sheath tumor of spine with a giant paraspinal and retrospinal subcutaneous extension
title_sort primary intraosseous malignant peripheral nerve sheath tumor of spine with a giant paraspinal and retrospinal subcutaneous extension
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551491/
https://www.ncbi.nlm.nih.gov/pubmed/23372973
http://dx.doi.org/10.4103/2152-7806.105096
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