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Also known as a "Vestibular Schwannoma."
We have selected the following expert medical opinion based on its clarity, reliability and accuracy. Credits: Sourced from the website Patient UK, authored by Dr Colin Tidy and Dr Helen Huins (see below). Please refer to your own medical practitioner for a final perspective, assessment or evaluation.
An acoustic neuroma is a rare tumour in the brain. The tumour grows on a nerve in the brain near to the ear. Acoustic neuromas tend to grow very slowly and don't usually spread to any distant part of the body.
Acoustic neuromas are rare. Between 1 and 20 people in every million worldwide are diagnosed each year with an acoustic neuroma. Acoustic neuromas account for about 6 in 100 brain tumors. They are more common in middle-aged adults and are rare in children. Acoustic neuromas seem to be more common in women than in men.
The cause of most acoustic neuromas is unknown. In less than 1 in 10 people, an acoustic neuroma is caused by neurofibromatosis type 2 (NF2). NF2 is a very rare genetic disorder that causes non-cancerous (benign) tumours of the nervous system. People with NF2 can also develop benign tumours on the spinal cord and the coverings of the brain.
It is not cancerous and so is called a benign tumour.
Acoustic neuromas grow from a type of cell called a Schwann cell. These cells cover the nerve cells in the body. This is why the tumour is also called a vestibular schwannoma.
The tumour grows along a nerve in the brain (these nerves are called cranial nerves) that is called the acoustic or vestibulocochlear nerve. This nerve controls your sense of hearing and also your balance. Therefore acoustic neuromas are sometimes called vestibular schwannomas.
Acoustic neuromas tend to grow very slowly and they don't spread to distant parts of the body. Sometimes they are too small to cause any problems or symptoms. Bigger acoustic neuromas can interfere with how the vestibulocochlear nerve works and so causes symptoms.
For most people with an acoustic neuroma, the cause is not known. About 7 out of every 100 acoustic neuromas are caused by a condition called neurofibromatosis type 2 (NF2). NF2 is a rare genetic disorder that causes benign tumours of the nervous system. It affects about 1 in 25,000 people.
Almost everyone with NF2 develops an acoustic neuroma on both nerves for hearing (acoustic nerves) - ie there is a tumour on the nerves on both sides of the head (bilateral). People with an acoustic neuroma but who don't have NF2 usually only develop a tumour on one side (unilateral). People with NF2 can also develop benign tumours on the spinal cord and the coverings (membranes) that surround the brain.
A small acoustic neuroma may cause no symptoms. If you do have symptoms from an acoustic neuroma, these usually develop very gradually, as the tumour is slow-growing.
A small acoustic neuroma may cause no symptoms. The symptoms that an acoustic neuroma can cause are very common. Remember that acoustic neuromas are very rare. You should see your doctor if you have any of these symptoms, but they are more likely to be due to other conditions than a brain tumour.
The most common symptoms of an acoustic neuroma are:
Other, common symptoms of acoustic neuroma include:
Less common symptoms of acoustic neuroma are:
Acoustic neuromas can be difficult to diagnose. If your GP suspects that you have an acoustic neuroma from your symptoms, you would probably be referred to a hospital ear, nose and throat (ENT) specialist.
Any initial tests will depend on the symptoms caused by the acoustic neuroma. If the tumour causes symptoms such as a headache or balance problems, you may also need to have other tests to check for other causes of these symptoms.
The best test to diagnose an acoustic neuroma is a magnetic resonance imaging (MRI) scan of the brain. An MRI scan uses a strong magnetic field and radio waves to take a detailed picture of your brain, and of the structures inside it. It is painless but it can be noisy and can make you feel anxious about being 'closed in' (claustrophobic).
Hearing tests are also needed if an acoustic neuroma is suspected. This is because one of the most common symptoms of an acoustic neuroma is hearing loss.
If you have a very small acoustic neuroma, your doctors might decide that the best way to treat you is just to observe and monitor it closely.
Acoustic neuromas are very slow-growing and may not cause any symptoms for a long time. Remember, acoustic neuromas are not cancerous (malignant) and do not spread, so it is quite safe to watch things for a while. Also, treatments can have complications and side-effects. Therefore, the risks and benefits of treatment have to be balanced. If observation is recommended, your condition will be monitored with regular scans.
The main treatments for acoustic neuroma are surgery or stereotactic radiosurgery.
The treatment you are offered will depend on:
The results of the tests and scans you have can also help to determine which type of treatment is best for you and your tumour.
Either a brain surgeon (neurosurgeon) or an ENT surgeon can operate to remove an acoustic neuroma, depending on its size and location on the vestibulocochlear nerve in the brain. The surgery is carried out under a general anaesthetic.
Most people with acoustic neuroma are treated with surgery, and about 95 in 100 tumours can be removed completely. Occasionally (about 5 cases in every 100), a small part of the tumour is left behind. This is usually because it is technically too difficult to remove the whole tumour and/or there is a risk of causing more damage to the nerve or other nearby structures.
If some of the acoustic neuroma is left remaining, it can often be treated with radiotherapy. After surgery for an acoustic neuroma, you will probably have to remain in hospital for a few days for monitoring. You should be fully recovered within 6-12 weeks, and, if your tumour was completely removed, you should not need any more treatment.
This is a newer type of treatment that can be used for acoustic neuromas. Stereotactic radiosurgery involves delivering radiation to an extremely well-defined area within the brain - where your acoustic neuroma is.
Stereotactic means locating a point using three-dimensional (3D) co-ordinates. In this instance, the point is the acoustic neuroma tumour within the brain. A metal frame (like a halo) is attached to your scalp and a series of scans is performed to show the exact position of the tumour. Stereotactic radiosurgery can be given with a normal radiotherapy machine, the CyberKnife® machine, or with a technique known as gamma knife treatment.
Stereotactic radiosurgery is a very specialised type of treatment and is only available in some large hospitals. These hospitals are usually ones with both neurosurgery and cancer treatment (oncology) centres. The main advantage of this treatment is to prevent tumour growth and preserve any remaining (residual) hearing. It tends to shrink rather than remove or destroy the acoustic neuroma. It can be used for very small tumours.
The possible complications due to the acoustic neuroma include:
The outlook (prognosis) is generally very good. Acoustic neuromas usually respond well to treatment and complications are uncommon. However, there is often some hearing loss in the affected ear after treatment.
Fewer than 5 in every 100 acoustic neuromas come back. So it is uncommon, but possible. It is more likely if you have NF2. It could cause any of the symptoms mentioned earlier, or any of the complications. After treatment for acoustic neuroma you will generally be followed up in an outpatient clinic to check for any symptoms or signs of it coming back.
Dr Colin Tidy
MBBS, MRCGP, MRCP, DCH
Dr Colin Tidy qualified as a doctor in 1983 and he has been writing for Patient since 2004. Dr Tidy has 25 years’ experience as a General Practitioner. He now works as a GP in Oxfordshire, with a special interest in teaching doctors and nurses, as well as medical students. In addition to writing many leaflets and articles for Patient, Dr Tidy has also contributed to medical journals and written a number of educational articles for General Practitioner magazines.
Dr Helen Huins
MB BS Lond, DCH, DRCOG, MRCGP, JCPTGP, DFFP
Helen qualified at Guy’s Hospital in 1989 and left London in 1990 to settle in the countryside. She works as a GP partner in a rural dispensing practice and is passionate about family medicine and continuity of care with interests in sport and nutrition. Helen has been a member of the EMIS authoring team since 1995.
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