anaplastic ependymoma

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Anaplastic ependymoma is a rare, malignant type of ependymoma that most often arises in the supratentorial region of the brain of children and young adults and that manifests with variable symptoms including headaches, nausea, vision impairment, memory loss and difficulty walking.


Synonyms

  • WHO grade III ependymal neoplasm
  • WHO grade III ependymal tumor
  • WHO grade III ependymal tumour
  • anaplastic ependymal neoplasm
  • anaplastic ependymal tumor
  • anaplastic ependymal tumour
  • anaplastic ependymoma
  • ependymal tumors
  • ependymal tumours
  • ependymoma, anaplastic, malignant
  • ependymoma, malignant
  • high-grade ependymoma
  • malignant ependymoma
  • undifferentiated ependymal neoplasm
  • undifferentiated ependymal tumor
  • undifferentiated ependymal tumour
  • undifferentiated ependymoma

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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