CASE REPORT
Os tumores intramedulares da medula espinhal são neoplasias raras, sendo o ependimoma o mais comum em adultos. O tratamento de escolha é cirúrgico por fornecer um diagnóstico histológico e prevenir disfunções neurológicas a longo prazo. O objetivo deste trabalho foi relatar o caso de um tumor intramedular extenso em um paciente jovem de 17 anos com história evolutiva de 3 anos de cervicalgia, déficit motor grave e disfunção esfincteriana, com RM evidenciando lesão intramedular acometendo C2 a T4, com ressecção completa. No exame anatomopatológico o resultado foi compatível com ependimoma grau 2. O paciente evoluiu com melhora significativa dos sintomas e déficits motores, mesmo após meningite, e atualmente está deambulando.
Intramedullary spinal cord tumors are rare neoplasms, with ependymoma being the most common in adults. The treatment of choice
for ependymomas is surgical, as it provides a histological diagnosis and prevents long-term neurological disorders. We report the case
of a 17-year-old patient with a 3-year history of neck pain and severe motor deficit and sphincter dysfunction, with MRI showing an
intramedullary lesion affecting C2 to T4, with complete resection. In the pathological examination, there was evidence of a grade 2
ependymoma. The patient evolved with significant improvement in symptoms and motor deficits and is currently walking.
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1 MD, Neurosurgeon, Neurosurgery Service, Hospital das Clínicas de Marília – HC FAMEMA, Marília, SP, Brazil.
2 Medicine Student, Internship Student of Medicine, University of Marília – UNIMAR, Marília, SP, Brazil.
3 MD, PhD, Neurosurgeon Chief, Neurosurgery Service, Hospital das Clínicas de Marília – HC FAMEMA, Marília, SP, Brazil.
Received Oct 31, 2022
Corrected Feb 6, 2023
Accepted Feb 6, 2023