Ependymoma is a type of central nervous system (CNS) tumor that develops from ependymal cells, which line the ventricles of the brain and the central canal of the spinal cord. It can occur in both children and adults and may develop in different areas of the brain or spinal cord. Modern classification increasingly incorporates molecular characteristics and tumor location, in addition to microscopic features, to define different ependymoma types.
Timely diagnosis and treatment are important because an ependymoma can compress or infiltrate nearby brain or spinal cord structures and may obstruct the normal flow of cerebrospinal fluid (CSF). Depending on its location and behaviour, the tumor can cause increased intracranial pressure, neurological impairment, hydrocephalus or spinal cord dysfunction. Early specialist evaluation helps determine the appropriate treatment strategy.
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Risk Factors
Ependymoma treatment is increasingly guided by molecular classification, tumor location, age, extent of surgical removal and disease dissemination. Modern pathology can identify molecular subgroups that provide information about tumor biology and prognosis. Advanced MRI techniques help define tumor anatomy and guide surgical planning.
Current treatment research includes improved molecular classification, targeted approaches for specific tumor alterations, precision radiation techniques and clinical trials investigating new therapies. For selected patients, advanced radiation techniques such as intensity-modulated radiation therapy (IMRT), proton therapy or stereotactic approaches may help deliver radiation while limiting exposure to surrounding healthy tissues.
Brain cancer surgery (craniotomy) : It is the primary treatment to diagnose, reduce the size of, or completely remove a brain tumor. The main goal is to safely remove as much of the tumor as possible while preserving vital brain functions like speech, movement, and cognitive abilities.
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Radiation Therapy : Radiation may be recommended after surgery for selected tumors, particularly when residual disease remains or when tumor characteristics indicate a higher risk of recurrence.
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Chemotherapy : It has a limited role in many newly diagnosed ependymomas but may be considered in selected situations, particularly in children or recurrent disease when other treatment options are limited.
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Treatment for Recurrent Disease: Recurrent ependymoma may require additional surgery, radiation, systemic therapy or a combination of approaches depending on the location and previous treatments.
Multidisciplinary and Supportive Care: Neurology, neurosurgery, radiation oncology, pediatric oncology, rehabilitation and supportive-care specialists may work together to address tumor control, neurological function and quality of life.
MediRehab (a chain of Rehab centres, part of MediGence) provides comprehensive rehabilitation services designed to support Ependymoma patients in India. These services include:









Mumbai, India

Chennai, India

Mumbai, India
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