The CERN Foundation is dedicated to helping you understand ependymoma. See below for a list fast facts about the disease.
Ependymoma tumor description
An ependymoma is a rare type of primary brain or spinal cord tumor
An ependymoma is a rare type of glial tumor; glial cells are the supportive cells of the brain
Primary brain and spinal cord tumors are those that start in the central nervous system (CNS)
These tumors are classified and graded according to their appearance when viewed through the microscope
Ependymomas can be found in children and adults
Ependymoma tumor incidence
Ependymoma tumors account for three to six percent of CNS tumors
Incidence in children:
- More common in children than adults
- The third most common pediatric brain tumor
- Over 90 percent occur in the brain
Incidence in adults:
Ependymoma staging and grading
- Ependymoma may spread throughout the CNS
- Spread outside of the CNS is rare
- All can recur (regrow)
- Graded on a scale of I to III (World Health Organization [WHO] Grading system)
- Grade I
Myxopapillary ependymomas
The myxopapillary ependymoma generally presents in the spinal canal of adults
Both tumors tend to grow slowly, especially the subependymoma
Grade II and III
Spinal cord and brain tumor symptoms
Symptoms depend on the tumor location. Any symptoms you have should be discussed with your doctor
Common brain tumor symptoms include:
Common spinal cord symptoms include:
Back pain
Weakness in the arms or legs
Numbness or tingling in the arms, legs or trunk
Problems going to the bathroom or controlling bowel or bladder function
Causes and treatment
The cause of ependymoma is not known. It rarely occurs in multiple family members, although does occur in people with Neurofibromatosis type 2.
Most people with ependymomas of any grade will undergo surgery to remove a tumor.
Depending on the tumor grade, location and how much of the tumor has been removed, radiation therapy is often given.