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About 1/3 of brain tumours diagnosed in the UK are astrocytomas. They affect adults and children.
If you or someone you know has just been diagnosed with an astrocytoma, you may be in a state of shock. This is a natural way to feel. Our Support and Information team can help answer any questions you may have or provide a listening ear if you need one.
Astrocytomas are the most common type of primary brain tumour and are part of a larger group of brain tumours called gliomas.
Astrocytomas grow from a type of cell in the brain called an astrocyte. These cells support and protect the nerves in the brain (neurons) and help to pass messages between them. As these cells are found throughout the brain, astrocytomas can occur in many different areas of the brain.
There are 4 main types of astrocytoma (pronounced ass-tro-sigh-toe-ma).
They’re most often found in children and young adults under the age of 20. They’re very rare in adults over 50 years. They’re equally common in males and females.
They occur most often in adults between the ages of 20 and 45. They’re more common in males than females.
Anaplastic means the cells divide rapidly and don’t look like normal cells in structure or function.
They’re more common in adults between the ages of 30 and 70 and are more common in males.
Grade 4 astrocytomas are usually called glioblastoma. You may hear them called glioblastoma multiforme, or GBM for short.
Being diagnosed with an astrocytoma can be overwhelming. Use BRIAN’s quality-of-life tracker to monitor how you feel and the symptoms you have. Then share this with your loved ones and healthcare team to show what you most need support with.
As astrocytomas grow from cells that are vital in processing information in the brain, astrocytomas can disrupt the function of whichever area of the brain they are growing in.
Pilocytic astrocytomas tend to grow in the cerebellum, which controls balance. They can also occur in the optic pathways, which are involved in sight.
The treatment for astrocytomas depends on the grade of the tumour, as well as its size and location.
Generally the first treatment for astrocytomas is neurosurgery to remove as much of the tumour as possible. This may be followed by radiotherapy and sometimes chemotherapy.
This may differ in children, who may be given chemotherapy rather than surgery or radiotherapy, and in people with pilocytic astrocytomas, who may be put on active monitoring (sometimes called watch and wait) before given surgery.
As with most brain tumours, it’s not known why astrocytomas start growing, although we do understand some of the risk factors involved.
It’s important to know that there is nothing you could have done, or avoided doing, that would have caused you or somebody you know to develop a brain tumour.
There are some genetic conditions that make people more likely to develop brain tumours, for example, neurofibromatosis type 1 (NF1). This is a genetic condition you are born with, that causes tumours to grow along the nerves and in the brain. Pilocytic astrocytomas occur in around 10% of people who have NF1.
This is impossible to answer for certain. While averages can be given, everybody is different – it will depend on so many factors – not only your tumour grade, size and location, but also your general health, your individual body chemistry, and how you respond to treatment.
If you need someone to talk to or advice on where to get help, our Support and Information team is available by phone, email or live-chat.
Three years ago, Alfie had a grade 1 pilocytic astrocytoma completely removed. Now he shares his experiences with fatigue and how he manages day to day.
By taking part in our Improving Brain Tumour Care surveys and sharing your experiences, you can help us improve treatment and care for everyone affected by a brain tumour.
If you have further questions, need to clarify any of the information on this page, or want to find out more about research and clinical trials, please contact our team:
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