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Dorsal spine osteoblastoma
Benign osteoblastoma is a rare primary neoplasm comprising less than 1% of primary bone tumors.[1] We report a case of a 20-year-old female patient presenting with progressive paraparesis over one year and back pain over the dorsal spine gradually increasing in severity over a year. Computerised tom...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802957/ https://www.ncbi.nlm.nih.gov/pubmed/27057242 http://dx.doi.org/10.4103/1793-5482.177661 |
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author | Bhargava, Pranshu Singh, Rahul Garg, Bharat B. |
author_facet | Bhargava, Pranshu Singh, Rahul Garg, Bharat B. |
author_sort | Bhargava, Pranshu |
collection | PubMed |
description | Benign osteoblastoma is a rare primary neoplasm comprising less than 1% of primary bone tumors.[1] We report a case of a 20-year-old female patient presenting with progressive paraparesis over one year and back pain over the dorsal spine gradually increasing in severity over a year. Computerised tomomography (CT) of the spine revealed a well-defined 3.5 × 3.0 cm mass heterodense expansile bony lesion arising from the lamina of the D12 vertebra, having lytic and sclerotic component and causing compromise of the bony spinal canal. D12 laminectomy and total excision of the tumor was done. |
format | Online Article Text |
id | pubmed-4802957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48029572016-04-07 Dorsal spine osteoblastoma Bhargava, Pranshu Singh, Rahul Garg, Bharat B. Asian J Neurosurg Case Report Benign osteoblastoma is a rare primary neoplasm comprising less than 1% of primary bone tumors.[1] We report a case of a 20-year-old female patient presenting with progressive paraparesis over one year and back pain over the dorsal spine gradually increasing in severity over a year. Computerised tomomography (CT) of the spine revealed a well-defined 3.5 × 3.0 cm mass heterodense expansile bony lesion arising from the lamina of the D12 vertebra, having lytic and sclerotic component and causing compromise of the bony spinal canal. D12 laminectomy and total excision of the tumor was done. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4802957/ /pubmed/27057242 http://dx.doi.org/10.4103/1793-5482.177661 Text en Copyright: © Asian Journal of Neurosurgery 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 Bhargava, Pranshu Singh, Rahul Garg, Bharat B. Dorsal spine osteoblastoma |
title | Dorsal spine osteoblastoma |
title_full | Dorsal spine osteoblastoma |
title_fullStr | Dorsal spine osteoblastoma |
title_full_unstemmed | Dorsal spine osteoblastoma |
title_short | Dorsal spine osteoblastoma |
title_sort | dorsal spine osteoblastoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802957/ https://www.ncbi.nlm.nih.gov/pubmed/27057242 http://dx.doi.org/10.4103/1793-5482.177661 |
work_keys_str_mv | AT bhargavapranshu dorsalspineosteoblastoma AT singhrahul dorsalspineosteoblastoma AT gargbharatb dorsalspineosteoblastoma |