Types
Vestibular schwannomas start in Schwann cells. These are cells that help to protect and support the nerve.
Usually, vestibular schwannomas develop in the Schwann cells covering the vestibulocochlear nerve. The vestibulocochlear nerve connects the brain to the inner ear. It controls hearing and balance.
Vestibular schwannomas do not spread to other parts of the body. Because they grow slowly over some years, you don’t usually have symptoms for some time.
When you do have symptoms, they can be:
hearing loss that usually affects one ear
ringing and buzzing sounds in 1 or both ears (tinnitus)
difficulty working out where sounds are coming from
dizziness or vertigo and problems with balance
numbness of the face
Find out more about the differences between benign and malignant brain tumours
Vestibular schwannomas are rare tumours. The risk of developing this tumour increases as you get older. The risk is greatest in those aged between 65 and 74 years old.
Rarely, vestibular schwannomas are caused by a genetic condition called NF2-related schwannomatosis. People with this condition are often diagnosed at a younger age with:
several benign tumours of the brain and spinal cord and
vestibular schwannomas in the nerves on both sides of the head (bilateral)
You have tests to diagnose a vestibular schwannoma. Your doctor checks the size of the tumour and its location. This helps your doctor plan your treatment. The tests you might have include:
hearing tests
MRI scan
CT scan
We have information about having MRI scans and CT scans in the getting diagnosed section
Your treatment plan depends on several factors including:
the size of your tumour
the symptoms you have
your age
your preferences
The team caring for you will talk to you about your treatment. They will consider the risk of further hearing loss as well as what you want.
You might not need treatment straight away and your doctors monitor you. Or you might have surgery or radiotherapy.
For a very small vestibular schwannoma, you might not need treatment straight away. Your doctor might recommend monitoring the tumour with regular MRI scans. This is called active surveillance. Your specialist will let you know how often you have your MRI scans.
Many small tumours don’t grow. If you are worried about symptoms between your appointments, contact your specialist. You might continue with monitoring. But it may be a sign that the tumour is growing and you might need treatment with either surgery or radiotherapy.
A brain specialist surgeon (neurosurgeon) might remove all the tumour or just a part. This depends on where the tumour is and its size.
There are different types of surgery that you can have. A common type is removing the tumour through a hole in your skull. This is usually a small cut above your ear or behind your ear.
To remove the tumour, it may be necessary to cut the hearing and balance nerve on the side where the tumour is. Your neurosurgeon will discuss the options with you.
You might have side effects after the operation. The side effects can include:
hearing loss on the side of the surgery, where the tumour was removed
problems with balance
infection of the membranes that surround the brain (meningitis)
headaches and neck pain
drooping of the face (facial palsy)
Read more about surgery for brain tumours
Radiotherapy means the use of radiation, usually X-rays, to treat cancer.
You might have one treatment. This is called stereotactic radiosurgery (SRS). Or you might have several treatments called stereotactic radiotherapy (SRT).
Your treatment depends on the size of the tumour and where it is. Both treatments target high doses of radiotherapy to the tumour.
The radiotherapy can stop the tumour growing and may reduce it in size.
Your specialist will tell you how long your treatment will last and what type of radiotherapy you will have.
The side effects depend on the type of treatment you have. They might include:
hearing loss
tiredness and fatigue
feeling sick
headaches
hair loss - in the treated area
skin problems in the area being treated – the skin can become dry and red. This usually improves a couple of weeks after the treatment has finished
facial weakness
Your radiotherapy team will explain more about your radiotherapy and the possible side effects.
We have information about stereotactic radiotherapy and radiosurgery
You have regular appointments with your doctor or nurse after treatment finishes. Your doctor examines you at each appointment. They ask how you are feeling, whether you have had any symptoms or side effects, and if you are worried about anything. You might have hearing tests. And you might also have MRI scans on some visits.
How often you have check ups depends on your individual situation.
Read more about follow up appointments after treatment for a brain tumour
You do not usually need to let the DVLA or DVA know if you have a vestibular schwannoma. But you must let them know if you’ve experienced sudden dizziness. Or you have a vestibular schwannoma in both ears.
Speak to your specialist nurse or doctor for advice if you are unsure about your symptoms.
Coping with a diagnosis of a brain tumour can be difficult, both practically and emotionally. It can be especially difficult when you have a rare tumour. Being well informed about the type of tumour you have, and its treatment can make it easier to cope.
Find out what you can do, who can help and how to cope with a brain tumour
Doctors are always trying to improve the diagnosis and treatment of brain tumours. As part of your treatment, your doctor might ask you to take part in a clinical trial. This might be to test a new treatment or look at different combinations of existing treatments.
Find out about the latest UK research and how you can take part in a clinical trial
Last reviewed: 12 May 2026
Next review due: 12 May 2029
Primary brain tumours are tumours that start in the brain. They can start anywhere in the brain and there are many different types of tumours.
There are many different types of brain tumours. They are usually named after the type of cell they develop from.
Treatment for a brain or spinal cord tumour depends on the type of tumour you have, where it is and your general health.
Survival depends on different factors such as the type, position and grade of your brain or spinal cord tumour.
It can be difficult to find out that you have a brain tumour. There is practical and emotional support available to help you, your family and your friends cope with a brain or spinal cord tumour.

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