Supratentorial extraventricular anaplastic ependymoma in a child

Muhammad Faisal Khilji1, Rana Shoaib Hamid, Asim Qureshi

  • 1Accident and Emergency Department, Sultan Qaboos University Hospital, Muscat, Oman.

BMJ Case Reports
|March 14, 2014
PubMed

Insights

A pediatric brain tumor, specifically an anaplastic ependymoma, was surgically removed from a young child. Post-surgery, the child recovered well and received radiotherapy.

Area of Science:

  • Pediatric Neurology
  • Neuro-oncology
  • Neurosurgery

Background:

  • Brain tumors are a significant cause of morbidity in children.
  • Anaplastic ependymoma is a rare and aggressive type of pediatric brain tumor.
  • Early diagnosis and surgical intervention are crucial for favorable outcomes.

Observation:

  • A young child presented with a two-week history of headache, focal seizures, left-sided weakness, and vomiting.
  • Brain imaging revealed a large intra-axial supratentorial mass in the right frontal lobe.
  • Initial differential diagnoses included astrocytoma, ependymoma, and choroid plexus papilloma.

Findings:

  • Histopathological examination confirmed the mass as a WHO grade III anaplastic ependymoma.
  • The child underwent complete surgical resection of the tumor.
  • Postoperative recovery was uneventful, followed by radiotherapy.

Implications:

  • This case highlights the importance of prompt neuroimaging in pediatric patients with focal neurological deficits.
  • Anaplastic ependymoma, even at a higher grade, can be managed effectively with multimodal treatment including surgery and radiotherapy.
  • Successful surgical resection and adjuvant therapy can lead to favorable outcomes in pediatric brain tumors.

Related Concept Videos