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Primary dorsal spine primitive neuroectodermal tumor in an adult patient: Case report and literature review

Primary spinal primitive neuroectodermal tumor (psPNET) is a rare entity with few cases reported in literature. We report a case of a 50-year-old female who presented to us with paraplegia and was diagnosed with extradural dorsal spine psPNET. The diagnosis was not suspected at presentation or on ra...

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Autores principales: Munjal, Satyashiva, Srivastava, Amit, Tucker, Shivya, Bakshi, Neha, Bhalla, Sunita, Mehta, VS
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763599/
https://www.ncbi.nlm.nih.gov/pubmed/29403254
http://dx.doi.org/10.4103/jcvjs.JCVJS_70_17
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author Munjal, Satyashiva
Srivastava, Amit
Tucker, Shivya
Bakshi, Neha
Bhalla, Sunita
Mehta, VS
author_facet Munjal, Satyashiva
Srivastava, Amit
Tucker, Shivya
Bakshi, Neha
Bhalla, Sunita
Mehta, VS
author_sort Munjal, Satyashiva
collection PubMed
description Primary spinal primitive neuroectodermal tumor (psPNET) is a rare entity with few cases reported in literature. We report a case of a 50-year-old female who presented to us with paraplegia and was diagnosed with extradural dorsal spine psPNET. The diagnosis was not suspected at presentation or on radiology but was established on histopathological examination. It is important to distinguish it from central nervous system primitive neuroectodermal tumors and from other spinal tumors since it follows a different clinical course and therapeutic outcome.
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spelling pubmed-57635992018-02-05 Primary dorsal spine primitive neuroectodermal tumor in an adult patient: Case report and literature review Munjal, Satyashiva Srivastava, Amit Tucker, Shivya Bakshi, Neha Bhalla, Sunita Mehta, VS J Craniovertebr Junction Spine Case Report Primary spinal primitive neuroectodermal tumor (psPNET) is a rare entity with few cases reported in literature. We report a case of a 50-year-old female who presented to us with paraplegia and was diagnosed with extradural dorsal spine psPNET. The diagnosis was not suspected at presentation or on radiology but was established on histopathological examination. It is important to distinguish it from central nervous system primitive neuroectodermal tumors and from other spinal tumors since it follows a different clinical course and therapeutic outcome. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5763599/ /pubmed/29403254 http://dx.doi.org/10.4103/jcvjs.JCVJS_70_17 Text en Copyright: © 2017 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
Munjal, Satyashiva
Srivastava, Amit
Tucker, Shivya
Bakshi, Neha
Bhalla, Sunita
Mehta, VS
Primary dorsal spine primitive neuroectodermal tumor in an adult patient: Case report and literature review
title Primary dorsal spine primitive neuroectodermal tumor in an adult patient: Case report and literature review
title_full Primary dorsal spine primitive neuroectodermal tumor in an adult patient: Case report and literature review
title_fullStr Primary dorsal spine primitive neuroectodermal tumor in an adult patient: Case report and literature review
title_full_unstemmed Primary dorsal spine primitive neuroectodermal tumor in an adult patient: Case report and literature review
title_short Primary dorsal spine primitive neuroectodermal tumor in an adult patient: Case report and literature review
title_sort primary dorsal spine primitive neuroectodermal tumor in an adult patient: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763599/
https://www.ncbi.nlm.nih.gov/pubmed/29403254
http://dx.doi.org/10.4103/jcvjs.JCVJS_70_17
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