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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

Apollo Hospitals Bannerghatta: Top Doctors, and Reviews
Apollo Hospitals Bannerghatta

Bangalore, India

Apollo Hospitals Bannerghatta located in Bengaluru, India is accredited by JCI, NABH. Also listed below are some of the most prominent infrastructural details:

  • Bed Capacity is 250
  • Largest and most sophisticated sleep laboratory in the world
  • Technological powerhouse with latest equipments
  • 120 slice CT angiogram
  • 3 Tesla MRI
  • Low energy & High energy Linear Accelerators
  • Navigation System in surgical procedures
  • 4-D Ultrasound for 4 dimensional sonography
  • Digital Fluoroscopy
  • Gamma Camera
  • Stereotactic Robotic Radio- surgery
  • Autologous Bone Marrow Transplantation
  • Robotic assisted surgeries
  • Thallium Laser-First in India
  • Holmium Laser-First in South India
  • Digital X-Ray-First in Karnataka
  • 100 plus consultants
  • Uses Y shaped stent for tracheoesophageal fistula
  • Four autologous chondrocyte implantations procedure is performed and several more like Spinal angiolipoma excision, Tibial tuberosity shift with MPSL reconstruction
  • Biggest series of airway stents in India
  • The Minimal Access Surgery Centre (MASC) centre of excellence
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HCG Kalinga Rao Road: Top Doctors, and Reviews
HCG Kalinga Rao Road

Bangalore, India

HCG Kalinga Rao Road located in Bengaluru, India is accredited by NABH, NABL. Also listed below are some of the most prominent infrastructural details:

  • Diagnostic facility equipped with state-of-the-art imaging technologies, such as 3T MRI, SPECT, PET-CT
  • Specialty laboratories provide state-of-the-art diagnostic facilities with expertise in oncology testing
  • The services provided under medical oncology include Haemato oncology, Pediatric oncology, Breast health, Preventive oncology, Daycare chemotherapy
  • Radiation oncology department adopts advanced technologies like CyberKnife Robotic Radiosurgery, TomoTherapy-H, Da Vinci, which allows cancer to be targeted with high accuracy
  • First Cancer Centre in India to introduce PET-CT technologies and Cyclotron
  • Consists of several beds and OTs with the latest equipment that meet high standards of sterility, and also comply with all international standards on operation theatre designs
  • Access to the latest technology like Linear Accelerator which allows the tumor to be treated with pinpoint accuracy
  • Equipped with Agility-Synergy linear accelerator, which allows accurate, image-guided radiotherapy to be provided safely and in a short time.
  • Have a unique facility that has BMT suites and a unique hemato-pathology lab. Conditions like Multiple Myeloma, Immune Deficiency Disorders, Leukaemia, Lymphomas, Aplastic Anaemia, Childhood Leukaemia, and certain Pediatric Cancers can be treated with Bone Marrow Transplants at the unit.
  • Ortho-Oncology clinic to be the first-of-its-kind in Bangalore, offering dedicated care for Musculoskeletal tumors
  • Round-the-clock extensive patient service helping diagnose cancer
  • Automated Breast Volume Scanner is the latest technology used for breast cancer detection
  • RTISTE linear accelerator used for various treatment approaches, including 3D conformal radiation therapy, Stereotactic
  • Radiosurgery (SRS), Intensity-Modulated Radiation Therapy (IMRT), and Stereotactic Body Radiotherapy
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Sarvodaya Hospital and Research Centre: Top Doctors, and Reviews
Sarvodaya Hospital and Research Centre

Faridabad, India

Sarvodaya Hospital and Research Centre located in Faridabad, India is accredited by NABH, NABL. Also listed below are some of the most prominent infrastructural details:

  • Sarvodaya Hospital has a 500 bed capacity which is inclusive of 65 ICU beds.
  • A dedicated dialysis unit for people with kidney conditions.
  • The hospital has a cancer center which makes cancer treatment a seamless process.
  • There is an upcoming oncology center in Sarvodaya Hospital Faridabad.
  • Technologies such as 128 Slice CT scan, 500 MA X-Ray, 1.5 Tesla MRI and Mammography facility.
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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.