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Schwannoma of the conus medullaris: a rare case

Intradural schwannoma of the conus medullaris is a rare form of spinal neoplasm, which commonly occurs in the lumbar region. Conus medullaris level is unusual for schwannomas. A 49-year-old woman presented with chronic sciatica, mild bladder dysfunction, and paresthesia in the buttocks. Magnetic res...

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Autores principales: Canbay, Suat, Hasturk, Askin Esen, Markoc, Fatma, Caglar, Sukru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sun Yat-sen University Cancer Center 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013335/
https://www.ncbi.nlm.nih.gov/pubmed/22085527
http://dx.doi.org/10.5732/cjc.011.10213
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author Canbay, Suat
Hasturk, Askin Esen
Markoc, Fatma
Caglar, Sukru
author_facet Canbay, Suat
Hasturk, Askin Esen
Markoc, Fatma
Caglar, Sukru
author_sort Canbay, Suat
collection PubMed
description Intradural schwannoma of the conus medullaris is a rare form of spinal neoplasm, which commonly occurs in the lumbar region. Conus medullaris level is unusual for schwannomas. A 49-year-old woman presented with chronic sciatica, mild bladder dysfunction, and paresthesia in the buttocks. Magnetic resonance imaging of the spine showed a mass lesion in the conus medullaris region with nerve compression. The tumor was completely resected and diagnosed histologically as schwannoma. The patient recovered after surgery. Clinical and radiologic features of this rare tumor are reviewed and are accompanied by literature findings.
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spelling pubmed-40133352014-05-15 Schwannoma of the conus medullaris: a rare case Canbay, Suat Hasturk, Askin Esen Markoc, Fatma Caglar, Sukru Chin J Cancer Case Research Intradural schwannoma of the conus medullaris is a rare form of spinal neoplasm, which commonly occurs in the lumbar region. Conus medullaris level is unusual for schwannomas. A 49-year-old woman presented with chronic sciatica, mild bladder dysfunction, and paresthesia in the buttocks. Magnetic resonance imaging of the spine showed a mass lesion in the conus medullaris region with nerve compression. The tumor was completely resected and diagnosed histologically as schwannoma. The patient recovered after surgery. Clinical and radiologic features of this rare tumor are reviewed and are accompanied by literature findings. Sun Yat-sen University Cancer Center 2011-12 /pmc/articles/PMC4013335/ /pubmed/22085527 http://dx.doi.org/10.5732/cjc.011.10213 Text en Chinese Journal of Cancer 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 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Case Research
Canbay, Suat
Hasturk, Askin Esen
Markoc, Fatma
Caglar, Sukru
Schwannoma of the conus medullaris: a rare case
title Schwannoma of the conus medullaris: a rare case
title_full Schwannoma of the conus medullaris: a rare case
title_fullStr Schwannoma of the conus medullaris: a rare case
title_full_unstemmed Schwannoma of the conus medullaris: a rare case
title_short Schwannoma of the conus medullaris: a rare case
title_sort schwannoma of the conus medullaris: a rare case
topic Case Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013335/
https://www.ncbi.nlm.nih.gov/pubmed/22085527
http://dx.doi.org/10.5732/cjc.011.10213
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