Ependymomas

About Ependymomas

With tumors, education and understanding are important as you navigate your diagnosis. An ependymal tumor usually begins in cells that line the fluid-filled spaces in the brain and around the spinal cord. An ependymal tumor may also be called an ependymoma. To learn more about ependymomas, read about the grades, symptoms and risk factors below.

Tumor Grades, Symptoms and Risk Factors of Ependymomas

Grades

Ependymoma (Grade 1 or 2):
A Grade 1 or 2 ependymoma grows slowly and has cells that look similar to normal cells. There are two types of Grade 1 ependymoma: myxopapillary ependymoma and subependymoma. A Grade 2 ependymoma grows in a ventricle (fluid-filled space in the brain) and its connecting paths or in the spinal cord. In some cases, a Grade 1 or 2 ependymoma can be cured.

Anaplastic ependymoma (Grade 3):
An anaplastic ependymoma grows quickly and spreads into nearby tissues. The tumor cells look different from normal cells. This type of tumor usually has a worse prognosis than a Grade 1 or 2 ependymoma.

Symptoms

Ependymomas are rare and can occur at any age, but most often occur in young children. Children with ependymoma may experience headaches and seizures. Ependymoma that occurs in adults is more likely to form in the spinal cord and may cause weakness in the part of the body controlled by the nerves that are affected by the tumor.

Some other possible symptoms are:

  • Changes in mood and personality
  • Headaches
  • Problems with coordination and balance
  • Seizures
  • Weakness in an arm or leg
Risk Factors

As with most central nervous system tumors, it’s not known what causes ependymomas, but research is in progress. Previous radiation to the head or a genetic (hereditary) condition called type II neurofibromatosis may be risk factors.

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