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Primitive neuroectodermal tumor in the spinal canal: A case report

Primitive neuroectodermal tumors (PNETs) are rare tumors of uncertain histogenesis that occur predominantly in children and young adults. The current study reports a case of PNET in a 60-year-old female, which presented clinically as an intraspinal tumor, causing symptoms of lower back pain, numbnes...

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Detalles Bibliográficos
Autores principales: MENG, XIAO-TONG, HE, SHI-SHENG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356409/
https://www.ncbi.nlm.nih.gov/pubmed/25789071
http://dx.doi.org/10.3892/ol.2015.2907
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author MENG, XIAO-TONG
HE, SHI-SHENG
author_facet MENG, XIAO-TONG
HE, SHI-SHENG
author_sort MENG, XIAO-TONG
collection PubMed
description Primitive neuroectodermal tumors (PNETs) are rare tumors of uncertain histogenesis that occur predominantly in children and young adults. The current study reports a case of PNET in a 60-year-old female, which presented clinically as an intraspinal tumor, causing symptoms of lower back pain, numbness and pain in the right lower extremity. The patient underwent tumorectomy. Following primary therapy, the symptoms of spinal cord compression were relieved. The patient underwent several courses of radiotherapy following surgery but refused to continue with chemotherapy. After a further four months, the tumors recurred and the patient succumbed to the disease.
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spelling pubmed-43564092015-03-18 Primitive neuroectodermal tumor in the spinal canal: A case report MENG, XIAO-TONG HE, SHI-SHENG Oncol Lett Articles Primitive neuroectodermal tumors (PNETs) are rare tumors of uncertain histogenesis that occur predominantly in children and young adults. The current study reports a case of PNET in a 60-year-old female, which presented clinically as an intraspinal tumor, causing symptoms of lower back pain, numbness and pain in the right lower extremity. The patient underwent tumorectomy. Following primary therapy, the symptoms of spinal cord compression were relieved. The patient underwent several courses of radiotherapy following surgery but refused to continue with chemotherapy. After a further four months, the tumors recurred and the patient succumbed to the disease. D.A. Spandidos 2015-04 2015-01-27 /pmc/articles/PMC4356409/ /pubmed/25789071 http://dx.doi.org/10.3892/ol.2015.2907 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
MENG, XIAO-TONG
HE, SHI-SHENG
Primitive neuroectodermal tumor in the spinal canal: A case report
title Primitive neuroectodermal tumor in the spinal canal: A case report
title_full Primitive neuroectodermal tumor in the spinal canal: A case report
title_fullStr Primitive neuroectodermal tumor in the spinal canal: A case report
title_full_unstemmed Primitive neuroectodermal tumor in the spinal canal: A case report
title_short Primitive neuroectodermal tumor in the spinal canal: A case report
title_sort primitive neuroectodermal tumor in the spinal canal: a case report
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356409/
https://www.ncbi.nlm.nih.gov/pubmed/25789071
http://dx.doi.org/10.3892/ol.2015.2907
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