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Surgical management of a thoracic chordoma: A case report and literature review

BACKGROUND: Chordomas are rare benign, but locally aggressive tumors that are regularly encountered in the clivus and sacrum. Although they are rarely found in the thoracic spine, they can contribute not only to local bone destruction and spinal instability, lead to cord compression, and major neuro...

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Detalles Bibliográficos
Autores principales: Moune, Michèle Yolande, Sayore, Christine Milena, Hemama, Mustapha, El Fatemi, Nizare, El Maaqili, Moulay-Rachid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888287/
https://www.ncbi.nlm.nih.gov/pubmed/35242429
http://dx.doi.org/10.25259/SNI_1227_2021
Descripción
Sumario:BACKGROUND: Chordomas are rare benign, but locally aggressive tumors that are regularly encountered in the clivus and sacrum. Although they are rarely found in the thoracic spine, they can contribute not only to local bone destruction and spinal instability, lead to cord compression, and major neurological deficits. CASE DESCRIPTION: A 56 year-old-male originally underwent a T12 laminectomy with debulking for a thoracic chordoma. Two years later, the lesion recurred contributing to a significant paraparesis. The new MR showed a T2 hyper intense lesion with huge epidural extension that warranted a 360° surgical decompression and fusion. The histopathology from both surgeries confirmed the diagnosis of a chordoma. CONCLUSION: Combined 360° decompression and fusion was warranted to resect a T12 chordoma that recurred 2 years following an original laminectomy with debulking procedure.