An ependymoma is a tumor that forms in your brain or spinal cord. Ependymoma is pronounced eh-PEN-de-MO-ma.
Ependymomas are primary tumors. They originate directly in the brain or spinal cord and don't migrate from other parts of the body.
They're a subtype of glioma. Ependymomas represent the sixth most frequent brain tumor among children. However, they may also strike adults.
Ependymomas are graded 1-3. Grade 1 has the slowest growth rate, and grade 3 has the fastest.
Grades 1 and 2 ependymomas are considered noncancerous (benign). These tumors usually grow slowly and have a low risk of metastasizing from their original site.
Grade 3 ependymomas are malignant, meaning they grow more aggressively and much faster than lower-grade ependymomas.
Besides grade, there are also several ependymoma types, such as:
An ependymoma may cause a wide range of symptoms depending on its location. These may include:
Babies and toddlers cannot tell you when they have discomfort or other symptoms; the only signs are those that come with a tumor growing. They may appear with:
Experts don't know what causes ependymomas. They may occur by accident when ependymal cells in the brain multiply, or they may be caused by genetic variations.
Some research has shown that individuals who have the genetic variations responsible for neurofibromatosis type 2 may be at higher risk of having ependymomas. But experts can't say for sure if they're related. They are still investigating this potential link.
A healthcare professional will diagnose an ependymoma with a physical examination, a neurological exam, and other tests. Your provider will ask about your symptoms and when you first noticed them.
Your provider might employ some of these tests to diagnose an ependymoma:
Your healthcare provider will treat an ependymoma with the following:
The five-year survival rate for ependymomas is almost 85%. That means about 85% of people are alive five years after diagnosis. However, this figure may not apply to you or your case. Your providers will tell you what to expect.
Many factors can influence your survival rate, such as:
There is no cure for cancer, though one can remove or destroy a grade 3 ependymoma with treatment.
Keep in mind that an ependymoma will recur at some point. The risk is much higher for grade 3 tumors. Depending on your age and overall health, your providers and surgeon will tell you what to expect.
Your doctor will tell you how often you will need follow-up visits to monitor any changes in your body. You also need regular imaging tests to monitor the ependymoma throughout treatment.
Tender Palm Super-Speciality Hospital offers advanced Ependymoma treatment in Lucknow, India, at an affordable cost. We have a team of experienced neurosurgeons and neuro-oncology specialists who provide accurate diagnosis and both surgical and non-surgical treatment options including tumor resection, radiation therapy, and chemotherapy procedures. Our Neurosurgery and Neuro-Oncology team has decades of experience in successfully treating Ependymoma in Lucknow, India.
Call us at +91-9076972161
Email at care@tenderpalm.com