CC BY-NC-ND 4.0 · Arquivos Brasileiros de Neurocirurgia: Brazilian Neurosurgery 2019; 38(01): 047-050
DOI: 10.1055/s-0039-1678587
Case Report | Relato de Caso
Thieme Revinter Publicações Ltda Rio de Janeiro, Brazil

Superior Sagittal Sinus Invasion by Malignant Glioma: Case Report and Literature Review

Invasão do seio sagital superior por glioma maligno: Relato de caso e revisão da literatura
Gonçalo Cerdeira Figueiredo
1   Department of Neurosurgery, Centro Hospitalar do Porto, Porto, Portugal
,
Sérgio Moreira
1   Department of Neurosurgery, Centro Hospitalar do Porto, Porto, Portugal
,
Célia Pinheiro
1   Department of Neurosurgery, Centro Hospitalar do Porto, Porto, Portugal
,
Alfredo Calheiros
1   Department of Neurosurgery, Centro Hospitalar do Porto, Porto, Portugal
› Author Affiliations
Further Information

Publication History

27 October 2018

08 January 2019

Publication Date:
08 February 2019 (online)

Abstract

Anaplastic oligodendrogliomas (AOs) correspond to ∼ 23% of all oligodendrogliomas. They correspond to a tumor with malignant histological characteristics, focal or diffuse, associated with a worse prognosis. In the present case report, we describe the case of a 30-year-old female submitted to resection of a right parietal lesion whose histology showed to be an AO. She underwent complementary treatment with chemotherapy and radiotherapy according to the Roger Stupp protocol. Four years after the initial diagnosis, there was tumor recurrence within the superior sagittal sinus, with no evidence of recurrence elsewhere. In the literature, we have found no similar published case reinforcing the rarity of this condition

Resumo

Oligodendrogliomas anaplásicos correspondem a ∼ 23% de todos os oligodendrogliomas. Eles correspondem a um tumor com características histológicas malignas, focais ou difusas, associadas a um pior prognóstico. Descrevemos aqui o caso de uma mulher de 30 anos de idade submetida à ressecção de uma lesão parietal direita, cuja histologia mostrou ser um oligodendroglioma anaplásico. A paciente foi submetida a tratamento complementar com quimioterapia e radioterapia de acordo com o protocolo de Roger Stupp. Quatro anos após o diagnóstico inicial, ocorreu recidiva tumoral no seio sagital superior, sem evidência de recorrência em outro local. Na literatura, não encontramos nenhum caso semelhante publicado reforçando a raridade desta condição.

 
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