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Multicentric intradural extramedullary ependymoma: Report of a rare case

Spinal ependymoma commonly presents as an intramedullary tumor. We present a rare case of multicentric intradural extramedullary spinal ependymoma. A 59 years old female presented to us with spastic quadriparesis for 10 months. Magnetic resonance imaging of the spinal cord showed discretely located...

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Autores principales: Vats, Atul, Ramdasi, Raghvendra, Zaveri, Gautam, Pandya, Sunil
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/PMC4530514/
https://www.ncbi.nlm.nih.gov/pubmed/26288550
http://dx.doi.org/10.4103/0974-8237.161596
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author Vats, Atul
Ramdasi, Raghvendra
Zaveri, Gautam
Pandya, Sunil
author_facet Vats, Atul
Ramdasi, Raghvendra
Zaveri, Gautam
Pandya, Sunil
author_sort Vats, Atul
collection PubMed
description Spinal ependymoma commonly presents as an intramedullary tumor. We present a rare case of multicentric intradural extramedullary spinal ependymoma. A 59 years old female presented to us with spastic quadriparesis for 10 months. Magnetic resonance imaging of the spinal cord showed discretely located enhancing tumor masses from at C1-C2, C6-C7, and D4 to L3 level. Subtotal resection of the symptomatic tumor at C6-C7 and D7-D9 was done. The patient underwent radiotherapy with 50.4 Gy. At follow-up of 11 months, patient is doing well. The relevant literature is reviewed.
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spelling pubmed-45305142015-08-18 Multicentric intradural extramedullary ependymoma: Report of a rare case Vats, Atul Ramdasi, Raghvendra Zaveri, Gautam Pandya, Sunil J Craniovertebr Junction Spine Case Report Spinal ependymoma commonly presents as an intramedullary tumor. We present a rare case of multicentric intradural extramedullary spinal ependymoma. A 59 years old female presented to us with spastic quadriparesis for 10 months. Magnetic resonance imaging of the spinal cord showed discretely located enhancing tumor masses from at C1-C2, C6-C7, and D4 to L3 level. Subtotal resection of the symptomatic tumor at C6-C7 and D7-D9 was done. The patient underwent radiotherapy with 50.4 Gy. At follow-up of 11 months, patient is doing well. The relevant literature is reviewed. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4530514/ /pubmed/26288550 http://dx.doi.org/10.4103/0974-8237.161596 Text en Copyright: © 2015 Journal of Craniovertebral Junction and Spine 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
Vats, Atul
Ramdasi, Raghvendra
Zaveri, Gautam
Pandya, Sunil
Multicentric intradural extramedullary ependymoma: Report of a rare case
title Multicentric intradural extramedullary ependymoma: Report of a rare case
title_full Multicentric intradural extramedullary ependymoma: Report of a rare case
title_fullStr Multicentric intradural extramedullary ependymoma: Report of a rare case
title_full_unstemmed Multicentric intradural extramedullary ependymoma: Report of a rare case
title_short Multicentric intradural extramedullary ependymoma: Report of a rare case
title_sort multicentric intradural extramedullary ependymoma: report of a rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530514/
https://www.ncbi.nlm.nih.gov/pubmed/26288550
http://dx.doi.org/10.4103/0974-8237.161596
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