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What is an Ependymoma?

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.

What is the Importance of Timely Treatment?

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.

What are the Common Symptoms of an Ependymoma?

  • Headache
  • Nausea and vomiting
  • Problems with balance or coordination
  • Difficulty walking
  • Seizures
  • Vision changes
  • Weakness or numbness
  • Back or neck pain in spinal tumors
  • Limb weakness or sensory changes
  • Changes in bladder or bowel function with spinal involvement
  • Hydrocephalus-related symptoms
  • Cognitive or behavioural changes in some brain tumors

Causes and Risk Factors of Ependymoma

Causes

  • The exact cause of most ependymomas is unknown. These tumors arise from genetic and molecular changes in ependymal cells, but in most patients there is no clearly identifiable environmental or lifestyle cause.
  • Some ependymomas have characteristic molecular alterations that help define their tumor subtype.

Risk Factors

  • Childhood or young age for certain ependymoma subtypes
  • Certain genetic conditions, particularly neurofibromatosis type 2 (NF2), which is associated with an increased risk of ependymal tumors
  • Specific molecular or genetic alterations within tumor cells

Latest Research and Technologies in the Treatment of Ependymoma in India

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.

Treatment options for Ependymoma

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.


Cost Start From 4500Explore Options

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.


Cost Start From 2500Explore Options

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.


Cost Start From 300Explore Options

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.

  • Clinical assessment:
    • Evaluation begins with a detailed medical history and neurological examination. Doctors assess symptoms such as headaches, seizures, balance problems, weakness, sensory changes, walking difficulties and bladder or bowel dysfunction.
    • For children, doctors may also evaluate developmental progress, school performance, and changes in behaviour.
    • Definitive diagnosis generally requires examination of tumor tissue obtained through surgery or biopsy. Pathological and molecular testing can help determine the ependymoma subtype and guide treatment planning.
  • Imaging Tests:
    • MRI Brain: Provides detailed visualisation of intracranial ependymomas and their relationship with surrounding structures.
    • MRI Spine: Important for spinal ependymomas and for assessing possible dissemination through the CSF pathways.
    • Contrast-Enhanced MRI: Helps define tumor margins, enhancement patterns and residual or recurrent disease.
    • CT Scan: May be used in selected situations, particularly when MRI is unavailable or additional structural information is needed.
    • Spinal Imaging/Neuraxis MRI: May be performed to assess for tumor spread along the brain and spinal cord.
    • CSF assessment: In selected patients, cerebrospinal fluid examination may be performed after imaging or surgery to evaluate possible tumor dissemination.

MediRehab (a chain of Rehab centres, part of MediGence) provides comprehensive rehabilitation services designed to support Ependymoma patients in India. These services include:

  • Physiotherapy: Helps improve strength, balance, coordination and mobility when the tumor or treatment has affected movement.
  • Occupational Therapy: Supports independence with daily activities and helps patients adapt to physical or neurological limitations.
  • Speech and Swallowing Therapy: May be recommended when a brain tumor or its treatment affects speech, communication or swallowing.
  • Neurorehabilitation: Structured rehabilitation can address motor, cognitive and functional difficulties following surgery or other neurological complications.
  • Long-Term Functional Support: Ongoing rehabilitation, nutritional support, psychological care and neurological follow-up may help patients manage persistent or changing functional needs.
  • Medicines do not usually eliminate a localised ependymoma but may be used to manage symptoms and treatment-related complications. Corticosteroids may be prescribed to reduce brain or spinal cord swelling around the tumor, while anti-seizure medicines may be used in patients who experience seizures. Pain medicines, anti-nausea medicines and other supportive treatments may also be required. Chemotherapy may be considered in selected recurrent or difficult-to-treat cases, particularly in pediatric patients, but its role varies according to tumor subtype and clinical circumstances.

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Hospitals for Ependymoma in India

Fortis Hospital: Top Doctors, and Reviews
Fortis Hospital

Bangalore, India

Fortis Hospital, Bannerghatta Road, Bangalore, has been a leading multi-speciality healthcare institution, offering advanced medical services with a patient-centric approach. The hospital features 400+ beds, state-of-the-art infrastructure, and experienced specialists across various specialities, providing comprehensive and compassionate care. Trusted by patients from India and abroad, Fortis Bannerghatta Road combines modern technology with high-quality treatment to deliver world-class healthcare.

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Ruby Hall Clinic: Top Doctors, and Reviews
Ruby Hall Clinic

Pune, India

Ruby Hall Clinic located in Pune, India is accredited by NABH. Also listed below are some of the most prominent infrastructural details:

  • Ruby Hall Clinic brought in Intensive Care and Coronary care units as early as in 1969.
  • It was the pioneer in terms of having achieved the first successful Kidney Transplant and test tube baby in Pune and being the initiator for Cobalt Therapy to ensure Cancer treatment.
  • Imaging advancement is being used in the hospital which is highly advanced known as Positron Emission Tomography.
  • Ruby Hall Clinic is in the possession of two cardiac cath labs and Linear Accelerators.
  • There are as many as 550 in-patient beds which is inclusive of 130 ICU beds.
  • Air Ambulance services are provided by the hospital.
  • There is a multi-organ transplant centre which began operations in the year 1997 and a Neuro Trauma stroke centre.
  • There is also the presence of an independent Stroke Trauma Unit which is fully equipped and enabled with the right units and healthcare personnel.
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Yashoda Hospital, Malakpet: Top Doctors, and Reviews
Yashoda Hospital, Malakpet

Hyderabad, India

Yashoda Hospital, Malakpet located in Hyderabad, India is accredited by NABH, NABL. Also listed below are some of the most prominent infrastructural details:

  • Multi-bed facility
  • High-tech labs, modular operation theaters
  • Advanced medical equipement
  • Dedicated rooms for patients with all facilities
  • State-of-art technology
  • 24/7 blood bank
  • State of the art Cardio-Thoracic Center with the latest CATH LAB Equipment & Modular steel operation theatre
  • Neurosurgery department equipped with an operating microscope, high-speed drill & stereotaxy
  • 24-hour Emergency services to take care of all kinds of trauma and other orthopedic emergencies
  • Pulmonology department equipped with modern gadgets.
  • One of the best PFT labs and bronchoscopy units
  • Nephrology services include Renal Biopsy, AV Fistulas, AV Grafts & Permanent Catheter Insertions, Hemodialysis; Temporary Access For Dialysis; Peritoneal Dialysis
  • Has a comprehensive cancer care unit following a trans-disciplinary & multi-modality approach
  • State-of-the-art services of Digital X rays, Flouroscopy, Ultrasonography, OPG, Mammography, CT 64 Slices, MRI, etc.
  • Airport Transfer Service
  • Scheduling Of All Medical Appointment
  • Processing Of Medical Second Opinion
  • Provide Language Interpreter
  • Special Dietary Needs / Religious Arrangement
  • Coordination Of Admissions Process
  • Cost Estimates For Anticipated Treatments
  • Foreign Exchange service
  • Billing and Finance Related Service
  • Providing Information Of Patient’s Relatives Back Home
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Why Choose India for Ependymoma Treatment?

  • Experienced Neuro-Oncology Teams: Patients can access multidisciplinary teams involving neurosurgeons, neuro-oncologists, radiation oncologists, neurologists and rehabilitation specialists.
  • Advanced Neuroimaging and Molecular Diagnosis: Major centres may offer high-resolution MRI, neuraxis imaging, advanced pathology and molecular testing to support tumor classification.
  • Advanced Neurosurgical Techniques: Selected patients may have access to image-guided and minimally invasive neurosurgical approaches designed to achieve maximal safe tumor removal.
  • Modern Radiation Therapy: Appropriate patients may have access to techniques such as IMRT, stereotactic radiation and proton therapy where available.
  • Comprehensive Rehabilitation and International Support: Rehabilitation services and international-patient departments can support recovery, follow-up and treatment coordination.

Frequently Asked Questions

Recovery depends on tumor location, size, extent of surgery, neurological effects and whether radiation or other treatment is required. Some patients recover within weeks, while others require several months of rehabilitation and follow-up.

Many patients can walk normally, particularly when the tumor does not affect motor pathways. Brain or spinal tumors that affect movement may cause weakness or balance problems and can require physiotherapy or other rehabilitation.

Major Indian cancer and neurosurgical centres may provide advanced MRI, image-guided neurosurgery, molecular pathology and modern radiation techniques for appropriately selected patients.

Many major Indian hospitals have international-patient departments that assist with medical records, specialist consultations, treatment coordination, travel arrangements, accommodation and follow-up care.

Consider a centre with experience in neuro-oncology and access to neurosurgery, neuropathology, molecular testing, radiation oncology and rehabilitation. For children, a multidisciplinary pediatric neuro-oncology team is particularly important.

No single success rate applies to all ependymomas. Outcomes depend on tumor location, molecular subtype, age, extent of safe tumor removal, spread of disease and response to additional treatment.

Neurosurgeons, neuro-oncologists, radiation oncologists and pediatric oncology teams in India manage ependymomas as part of specialised neuro-oncology care. Experience should be assessed according to the patient's age and specific tumor characteristics.

Risks depend on the tumor location and treatment. Surgery may cause bleeding, infection, seizures or neurological deficits, while radiation and medicines can cause treatment-specific side effects. The treating team should explain individual risks before therapy.

A doctor should evaluate persistent or worsening symptoms such as headaches, vomiting, seizures, weakness, balance problems, or changes in bladder or bowel function. Sudden severe neurological symptoms, seizures or loss of consciousness require emergency medical assessment.

Ependymoma does not typically cause physical deformities. However, tumors affecting the brain or spinal cord can sometimes result in lasting weakness, movement difficulties, sensory changes or other neurological impairments.

Yes. Symptoms, neurological deficits, treatment effects and the need for long-term monitoring can affect mobility, education, work, communication, independence and emotional well-being. Rehabilitation and supportive care can help address these challenges.

An untreated ependymoma may continue to grow and compress or damage nearby neurological structures. Depending on its location and behaviour, it can cause progressive neurological impairment, hydrocephalus, seizures or other complications.

Most ependymomas cannot be prevented because their exact causes are not known. People with certain inherited conditions associated with increased tumor risk may require specialist surveillance according to their genetic and clinical circumstances.

Ependymoma can occur at any age but has different patterns across age groups and molecular subtypes. Some forms are more frequently seen in children, while spinal ependymomas are more common in adults. Certain inherited conditions are also associated with an increased risk of ependymal tumors.