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Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review
BACKGROUND: Hereditary multiple osteochondromas (HMOs) are a rare genetic disorder characterized by the formation of multiple benign osteochondromas that can undergo malignant transformation into chondrosarcoma. CASE DESCRIPTION: A 24-year-old male with a history of HMO and osteochondroma surgery 4...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695461/ http://dx.doi.org/10.25259/SNI_797_2023 |
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author | Silva, José Elmano Monteiro, Gabriel de Almeida Silva, Stefanie Torres e Bezerra, Gabriel Marinheiro dos Santos Cavalcante-Neto, Joaquim Francisco Bezerra, Diego de Aragão Vasconcelos, Janssen Loiola Melo Leal, Paulo Roberto Lacerda |
author_facet | Silva, José Elmano Monteiro, Gabriel de Almeida Silva, Stefanie Torres e Bezerra, Gabriel Marinheiro dos Santos Cavalcante-Neto, Joaquim Francisco Bezerra, Diego de Aragão Vasconcelos, Janssen Loiola Melo Leal, Paulo Roberto Lacerda |
author_sort | Silva, José Elmano |
collection | PubMed |
description | BACKGROUND: Hereditary multiple osteochondromas (HMOs) are a rare genetic disorder characterized by the formation of multiple benign osteochondromas that can undergo malignant transformation into chondrosarcoma. CASE DESCRIPTION: A 24-year-old male with a history of HMO and osteochondroma surgery 4 years ago, presented with back pain and paresthesias. The magnetic resonance showed a right paravertebral infiltrating mass at the T12–L1 level causing spinal cord compression. Following en bloc resection of the tumor, the patient’s symptoms/ signs resolved. The final pathological diagnosis was consistent with a chondrosarcoma. CONCLUSION: Chondrosarcomas secondary to HMO with spinal cord compression are rare. These patients often presenting with significant myelopathy/cord compression should undergo gross total resection where feasible to achieve the best outcomes. |
format | Online Article Text |
id | pubmed-10695461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-106954612023-12-05 Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review Silva, José Elmano Monteiro, Gabriel de Almeida Silva, Stefanie Torres e Bezerra, Gabriel Marinheiro dos Santos Cavalcante-Neto, Joaquim Francisco Bezerra, Diego de Aragão Vasconcelos, Janssen Loiola Melo Leal, Paulo Roberto Lacerda Surg Neurol Int Case Report BACKGROUND: Hereditary multiple osteochondromas (HMOs) are a rare genetic disorder characterized by the formation of multiple benign osteochondromas that can undergo malignant transformation into chondrosarcoma. CASE DESCRIPTION: A 24-year-old male with a history of HMO and osteochondroma surgery 4 years ago, presented with back pain and paresthesias. The magnetic resonance showed a right paravertebral infiltrating mass at the T12–L1 level causing spinal cord compression. Following en bloc resection of the tumor, the patient’s symptoms/ signs resolved. The final pathological diagnosis was consistent with a chondrosarcoma. CONCLUSION: Chondrosarcomas secondary to HMO with spinal cord compression are rare. These patients often presenting with significant myelopathy/cord compression should undergo gross total resection where feasible to achieve the best outcomes. Scientific Scholar 2023-11-03 /pmc/articles/PMC10695461/ http://dx.doi.org/10.25259/SNI_797_2023 Text en Copyright: © 2023 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, 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 Silva, José Elmano Monteiro, Gabriel de Almeida Silva, Stefanie Torres e Bezerra, Gabriel Marinheiro dos Santos Cavalcante-Neto, Joaquim Francisco Bezerra, Diego de Aragão Vasconcelos, Janssen Loiola Melo Leal, Paulo Roberto Lacerda Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review |
title | Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review |
title_full | Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review |
title_fullStr | Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review |
title_full_unstemmed | Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review |
title_short | Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review |
title_sort | chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: a case report and systematic review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695461/ http://dx.doi.org/10.25259/SNI_797_2023 |
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