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Rapidly Enlarging Pediatric Cortical Ependymoma

  • Yamasaki, Kouji (Department of Neurosurgery, Faculty of Medicine, University of Miyazaki) ;
  • Yokogami, Kiyotaka (Department of Neurosurgery, Faculty of Medicine, University of Miyazaki) ;
  • Yamashita, Shinji (Department of Neurosurgery, Faculty of Medicine, University of Miyazaki) ;
  • Takeshima, Hideo (Department of Neurosurgery, Faculty of Medicine, University of Miyazaki)
  • 투고 : 2014.03.17
  • 심사 : 2014.05.13
  • 발행 : 2015.06.28

초록

We report a 10-year-old boy with supratentorial cortical ependymoma that rapidly grew in the course of 3 years. He suffered generalized seizures when he was 5 years old; MRI showed a small cortical lesion in the right postcentral gyrus. MRI performed 2 years later revealed no changes. For the next 3 years he was free of seizures. However, at the age of 10 he again suffered generalized seizures and MRI disclosed a large parietal tumor. It was resected totally and he remains free of neurological deficits. The histopathological diagnosis was ependymoma. Pediatric supratentorial cortical ependymomas are extremely rare. We recommend including cortical ependymoma as a differential diagnosis in pediatric patients with cortical mass lesions presenting with seizures and careful follow-up even in the absence of symptoms because these tumors may progress.

키워드

참고문헌

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피인용 문헌

  1. Supratentorial pediatric cortical ependymomas: a comprehensive retrospective study vol.44, pp.3, 2021, https://doi.org/10.1007/s10143-020-01336-w