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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2023
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.
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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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