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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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Detalles Bibliográficos
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
Descripción
Sumario: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.