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Burkitt lymphoma (BL) is a rare type of fast-growing non-Hodgkin lymphoma (NHL). It develops when B-cells (also called B-lymphocytes) become abnormal. B-cells are white blood cells that fight infection. There are different types of BL. The most common type in the UK is often called sporadic BL.
This information is about Burkitt lymphoma in adults. BL can also affect children. If you need more information about lymphoma in children, you can contact the Children’s Cancer and Leukaemia Group.
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BL may cause a lump or mass in the tummy area (abdomen). This can cause pain and swelling, feeling sick (nausea) and diarrhoea.
It may also cause painless swellings in the neck, armpit or groin. This is caused by lymphoma cells building up in the lymph nodes, which makes them bigger. Often lymph nodes in more than one part of the body are affected. If BL is in lymph nodes in the chest, throat or jaw, this may cause a sore throat, difficulty swallowing or breathlessness.
General symptoms may include loss of appetite and tiredness.
Some people also have:
- drenching night sweats
- high temperatures (fevers) with no obvious cause
- unexplained weight loss
Doctors call this group of symptoms B symptoms.
The causes of sporadic BL are mostly unknown.
There is another type of BL that can affect people in the UK if they have a weakened immune system. This is called immunodeficiency-associated BL. The body's immune system can be weakened by:
- conditions such as human immunodeficiency virus (HIV) infection
- drugs called immuno-suppressants (used after an organ transplant or to treat autoimmune disease).
Like other cancers, BL is not infectious and cannot be passed on to other people.
The most important test for diagnosing lymphoma is a biopsy. A doctor or nurse will take a sample of tissue from the affected area. The most common place to take a biopsy from is an enlarged lymph node. This is called a lymph node biopsy. You may have all or a part of the lymph node removed. The tissue will be sent to a laboratory for testing.
The results of your tests help your doctors find out how many areas of the body are affected by lymphoma and where these areas are. This is called staging.
Lymphomas are also grouped as either low-grade or high-grade. Low-grade lymphomas are usually slow growing and high-grade lymphomas grow more quickly. BL is a high-grade, lymphoma.
We have more information about staging and grading of non-Hodgkin lymphoma.
A team of specialists will meet to discuss the best possible treatment for you. This is called a multidisciplinary team (MDT).
Your doctor or cancer specialist or nurse will explain the different treatments and their side effects. They will also talk to you about things to consider when making treatment decisions.
The main treatment for BL is a combination of drugs that includes:
Chemotherapy can be given into the spinal fluid to allow the drug to reach the spinal cord and brain (central nervous system). This is called intrathecal chemotherapy. It may be given to treat lymphoma or to reduce the risk of lymphoma developing in these areas.The following chemotherapy drugs may also be used in different combinations to treat BL:
You may have some treatments as part of a clinical trial.
You usually stay in hospital while you are having treatment for BL.
The drugs used may cause the lymphoma cells to break down very quickly. This can cause chemical imbalances in the blood that affect the kidneys and the heart. This is called tumour lysis syndrome (TLS).
You doctor and nurse will monitor you closely for signs of TLS and give you drugs to help prevent it. You usually have a drug called rasburicase as a drip (infusion) and extra fluids as a drip to help protect your kidneys. You may only need rasburicase with the first treatment for BL. After that, you can have tablets called allopurinol instead.
After treatment, some people are cured of BL. But for others, cancer may come back after treatment. If this happens, you may be able to have further treatment.
You have regular follow-up appointments after treatment. These appointments are a good opportunity for you to talk to your doctor or nurse about any concerns you have. Your doctor will want to know how you are feeling generally, and to check you are recovering from any side effects of treatment.
Sometimes a side effect may continue or develop months or years after treatment. This is called a late effect.
We have more information about long-term and late effects of treatment for lymphoma.
Everyone has their own way of dealing with illness and the different emotions they experience. You may find it helpful to talk things over with family and friends or your doctor or nurse.
Macmillan can offer emotional, practical and financial help and support.
The organisations below also offer information and support:
Bloodwise offers support and information to people affected by blood cancers, including lymphoma.
- Lymphoma Action
Lymphoma Action gives emotional support, advice and information on all aspects of Hodgkin lymphoma and non-Hodgkin lymphoma. It has a national network of people with lymphoma, and local groups.