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Chordoma of the lumbar spine—A potential diagnosis not to be forgotten!

Chordoma is a rare, malignant neoplasm thought to develop from the notochord. It most commonly occurs in the base of the cranium or the sacro-coccygeal region but around 15%-20% affect the vertebral body. Extra-lesional resection with or without adjuvant radiotherapy is generally accepted as the mai...

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Autores principales: Elafram, Rafik, Abcha, Oussama, Romdhane, Majdi Ben, Sghaier, Majdi, Annabi, Hedi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691436/
https://www.ncbi.nlm.nih.gov/pubmed/36439933
http://dx.doi.org/10.1016/j.radcr.2022.10.037
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author Elafram, Rafik
Abcha, Oussama
Romdhane, Majdi Ben
Sghaier, Majdi
Annabi, Hedi
author_facet Elafram, Rafik
Abcha, Oussama
Romdhane, Majdi Ben
Sghaier, Majdi
Annabi, Hedi
author_sort Elafram, Rafik
collection PubMed
description Chordoma is a rare, malignant neoplasm thought to develop from the notochord. It most commonly occurs in the base of the cranium or the sacro-coccygeal region but around 15%-20% affect the vertebral body. Extra-lesional resection with or without adjuvant radiotherapy is generally accepted as the mainstay of treatment for this slow-growing tumor. We present a case whereby a patient with an extensive vertebral body lesion causing caudal compression, treated with spinal decompression and posterior stabilization. This case highlights the importance of pre-operative tissue diagnosis, and that, although rare (0.8 per 100,000), chordoma should always be considered.
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spelling pubmed-96914362022-11-26 Chordoma of the lumbar spine—A potential diagnosis not to be forgotten! Elafram, Rafik Abcha, Oussama Romdhane, Majdi Ben Sghaier, Majdi Annabi, Hedi Radiol Case Rep Case Report Chordoma is a rare, malignant neoplasm thought to develop from the notochord. It most commonly occurs in the base of the cranium or the sacro-coccygeal region but around 15%-20% affect the vertebral body. Extra-lesional resection with or without adjuvant radiotherapy is generally accepted as the mainstay of treatment for this slow-growing tumor. We present a case whereby a patient with an extensive vertebral body lesion causing caudal compression, treated with spinal decompression and posterior stabilization. This case highlights the importance of pre-operative tissue diagnosis, and that, although rare (0.8 per 100,000), chordoma should always be considered. Elsevier 2022-11-24 /pmc/articles/PMC9691436/ /pubmed/36439933 http://dx.doi.org/10.1016/j.radcr.2022.10.037 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Elafram, Rafik
Abcha, Oussama
Romdhane, Majdi Ben
Sghaier, Majdi
Annabi, Hedi
Chordoma of the lumbar spine—A potential diagnosis not to be forgotten!
title Chordoma of the lumbar spine—A potential diagnosis not to be forgotten!
title_full Chordoma of the lumbar spine—A potential diagnosis not to be forgotten!
title_fullStr Chordoma of the lumbar spine—A potential diagnosis not to be forgotten!
title_full_unstemmed Chordoma of the lumbar spine—A potential diagnosis not to be forgotten!
title_short Chordoma of the lumbar spine—A potential diagnosis not to be forgotten!
title_sort chordoma of the lumbar spine—a potential diagnosis not to be forgotten!
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691436/
https://www.ncbi.nlm.nih.gov/pubmed/36439933
http://dx.doi.org/10.1016/j.radcr.2022.10.037
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