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Thoracic intramedullary chordoma without bone involvement: a rare clinical entity

An 8-year-old boy presented with a 1-year history of low backache, followed by paraparesis and urinary incontinence. MRI of the thoracic spine revealed an intramedullary, intensely contrast-enhancing lesion extending from T11 to L1 vertebral level, consistent with astrocytoma, ependymoma or haemangi...

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Autores principales: Faheem, Mohd, Zeeshan, Qazi, Ojha, Balkrishna, Agrawal, Preeti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986013/
https://www.ncbi.nlm.nih.gov/pubmed/27469385
http://dx.doi.org/10.1136/bcr-2016-216101
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author Faheem, Mohd
Zeeshan, Qazi
Ojha, Balkrishna
Agrawal, Preeti
author_facet Faheem, Mohd
Zeeshan, Qazi
Ojha, Balkrishna
Agrawal, Preeti
author_sort Faheem, Mohd
collection PubMed
description An 8-year-old boy presented with a 1-year history of low backache, followed by paraparesis and urinary incontinence. MRI of the thoracic spine revealed an intramedullary, intensely contrast-enhancing lesion extending from T11 to L1 vertebral level, consistent with astrocytoma, ependymoma or haemangioblastoma. A diagnosis of intramedullary chordoma was made on tissue biopsy and immunohistochemical study. This is the second report of an intramedullary chordoma without bone involvement in English literature. After 6 months of follow-up, patient showed good clinical outcome in terms of improvement in power in lower limbs and backache.
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spelling pubmed-49860132016-08-19 Thoracic intramedullary chordoma without bone involvement: a rare clinical entity Faheem, Mohd Zeeshan, Qazi Ojha, Balkrishna Agrawal, Preeti BMJ Case Rep Article An 8-year-old boy presented with a 1-year history of low backache, followed by paraparesis and urinary incontinence. MRI of the thoracic spine revealed an intramedullary, intensely contrast-enhancing lesion extending from T11 to L1 vertebral level, consistent with astrocytoma, ependymoma or haemangioblastoma. A diagnosis of intramedullary chordoma was made on tissue biopsy and immunohistochemical study. This is the second report of an intramedullary chordoma without bone involvement in English literature. After 6 months of follow-up, patient showed good clinical outcome in terms of improvement in power in lower limbs and backache. BMJ Publishing Group 2016-07-28 /pmc/articles/PMC4986013/ /pubmed/27469385 http://dx.doi.org/10.1136/bcr-2016-216101 Text en 2016 BMJ Publishing Group Ltd This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Article
Faheem, Mohd
Zeeshan, Qazi
Ojha, Balkrishna
Agrawal, Preeti
Thoracic intramedullary chordoma without bone involvement: a rare clinical entity
title Thoracic intramedullary chordoma without bone involvement: a rare clinical entity
title_full Thoracic intramedullary chordoma without bone involvement: a rare clinical entity
title_fullStr Thoracic intramedullary chordoma without bone involvement: a rare clinical entity
title_full_unstemmed Thoracic intramedullary chordoma without bone involvement: a rare clinical entity
title_short Thoracic intramedullary chordoma without bone involvement: a rare clinical entity
title_sort thoracic intramedullary chordoma without bone involvement: a rare clinical entity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986013/
https://www.ncbi.nlm.nih.gov/pubmed/27469385
http://dx.doi.org/10.1136/bcr-2016-216101
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