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Acute spinal cord compression caused by atypical vertebral hemangioma

Vertebral hemangioma is common, benign lesion that occurs mostly in the body of vertebral bones and is mostly asymptomatic although they may occasionally extend into the posterior elements. An isolated location in the neural arch of vertebrae is extremely rare. An acute spinal cord compression by an...

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Autores principales: Bellasri, Salah, Fatihi, Jamal, Elktaibi, Abderrahim, El Asri, Abad Cherif
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/PMC5634116/
https://www.ncbi.nlm.nih.gov/pubmed/29021681
http://dx.doi.org/10.4103/jcvjs.JCVJS_14_17
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author Bellasri, Salah
Fatihi, Jamal
Elktaibi, Abderrahim
El Asri, Abad Cherif
author_facet Bellasri, Salah
Fatihi, Jamal
Elktaibi, Abderrahim
El Asri, Abad Cherif
author_sort Bellasri, Salah
collection PubMed
description Vertebral hemangioma is common, benign lesion that occurs mostly in the body of vertebral bones and is mostly asymptomatic although they may occasionally extend into the posterior elements. An isolated location in the neural arch of vertebrae is extremely rare. An acute spinal cord compression by an exceptional hemangioma involving spinous process of the seventh thoracic vertebra and respecting vertebral body in a 40-year-old woman is reported. On magnetic resonance imaging of the spine, the lesion was hypointense on T1-weighted image, hyperintense on T2-weited image, and enhancing avidly, causing compression of spinal cord. Our case is exceptional by the rapidly character of symptom installation and by atypical and elective involvement of spinous process.
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spelling pubmed-56341162017-10-11 Acute spinal cord compression caused by atypical vertebral hemangioma Bellasri, Salah Fatihi, Jamal Elktaibi, Abderrahim El Asri, Abad Cherif J Craniovertebr Junction Spine Case Report Vertebral hemangioma is common, benign lesion that occurs mostly in the body of vertebral bones and is mostly asymptomatic although they may occasionally extend into the posterior elements. An isolated location in the neural arch of vertebrae is extremely rare. An acute spinal cord compression by an exceptional hemangioma involving spinous process of the seventh thoracic vertebra and respecting vertebral body in a 40-year-old woman is reported. On magnetic resonance imaging of the spine, the lesion was hypointense on T1-weighted image, hyperintense on T2-weited image, and enhancing avidly, causing compression of spinal cord. Our case is exceptional by the rapidly character of symptom installation and by atypical and elective involvement of spinous process. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5634116/ /pubmed/29021681 http://dx.doi.org/10.4103/jcvjs.JCVJS_14_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
Bellasri, Salah
Fatihi, Jamal
Elktaibi, Abderrahim
El Asri, Abad Cherif
Acute spinal cord compression caused by atypical vertebral hemangioma
title Acute spinal cord compression caused by atypical vertebral hemangioma
title_full Acute spinal cord compression caused by atypical vertebral hemangioma
title_fullStr Acute spinal cord compression caused by atypical vertebral hemangioma
title_full_unstemmed Acute spinal cord compression caused by atypical vertebral hemangioma
title_short Acute spinal cord compression caused by atypical vertebral hemangioma
title_sort acute spinal cord compression caused by atypical vertebral hemangioma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634116/
https://www.ncbi.nlm.nih.gov/pubmed/29021681
http://dx.doi.org/10.4103/jcvjs.JCVJS_14_17
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