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MALT lymphoma is a slow-growing type of non-Hodgkin lymphoma. Like all lymphomas, it is a cancer of the lymphatic system, which is part of the body’s immune system. It develops when white blood cells called B-lymphocytes become abnormal and begin to grow in an uncontrolled way.
MALT lymphoma affects lymphatic tissue called mucosa-associated lymphoid tissue (MALT). Mucosa is the name for the tissue that lines some organs in the body.
The most common area for MALT lymphoma to develop is the stomach. But it may start in other parts of the body, including the:
- thyroid gland
- salivary gland
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The symptoms depend on where in the body the lymphoma started.
For example, MALT lymphoma in the stomach may cause symptoms such as:
- loss of appetite
- feeling sick (nausea).
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.
MALT lymphomas usually start in areas of the body where there has been long-term inflammation. This may be due to an infection or autoimmune condition in that area. In autoimmune conditions, the body’s immune system attacks body tissue rather than protecting it.
MALT lymphoma is not infectious and cannot be passed on to other people.
Most MALT lymphomas in the stomach are linked to infection with bacteria called Helicobacter pylori (H. pylori). If H. pylori infection is not treated, it can cause long-term inflammation of the stomach lining. Over time, this may lead to MALT lymphoma developing.
Other types of bacterial infection have been linked to MALT lymphoma in the skin, eye and bowel.
Long-term infection with the virus hepatitis C is also a risk factor for MALT lymphoma.
Autoimmune conditions such as Hashimoto’s thyroiditis and Sjögren’s syndrome have been linked to MALT lymphoma in the thyroid gland, salivary glands and lungs.
- In Hashimoto’s thyroiditis, the immune system attacks the thyroid gland. This makes it underactive.
- In Sjögren’s syndrome, the immune system attacks glands that make fluid. This causes dry eyes and a dry mouth.
MALT lymphoma is diagnosed by doctors taking tissue samples (biopsies) from the affected area. The biopsies are sent to a laboratory for testing and to be examined under a microscope.
If you might have MALT lymphoma in the stomach, your doctor will do an endoscopy. During the endoscopy, they take biopsies from different areas of the stomach.
You can read more about further tests you may have in our information about non-Hodgkin lymphoma.
Waiting for test results can be a difficult time. It may help to talk to your family, friends or specialist nurse.
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.
In MALT lymphoma of the stomach, doctors also measure how far the lymphoma has spread from the lining of the stomach into deeper layers of the stomach.
Most MALT lymphomas are diagnosed at an early stage.
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.
MALT lymphoma is a low-grade lymphoma, but rarely it can change (transform) to become 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.
Treatment for MALT lymphoma is usually very successful.
Treatment depends on the type of MALT lymphoma and the stage it is at.
Watch and wait
If the lymphoma is growing very slowly and not causing any problems, you may not need any treatment for some time. Your doctor will monitor you closely so that if the lymphoma does start to grow, they can start your treatment. This is called watch and wait.
If you have MALT lymphoma in the stomach, you will have tests to check for an infection caused by the bacteria called H. pylori. If you have this, you will have a treatment called triple therapy to get rid of the infection. This involves taking a course of 2 antibiotics and a treatment to reduce the amount of acid made by the stomach.
Getting rid of H. pylori may clear all signs of the lymphoma (called remission). But this may take several months. After triple therapy, you will have regular endoscopies to check for lymphoma in the stomach. This is to check the lymphoma is shrinking and that you do not need further treatment.
People who have MALT lymphoma of the eye (orbital MALT) may also be treated with antibiotics. This may make the lymphoma shrink or disappear. It can take several months for this to happen.
Radiotherapy may be used to treat localised MALT lymphoma in the stomach that:
- is not caused by H. pylori
- has not got better with antibiotic treatment.
Radiotherapy may also be used to treat localised MALT lymphoma in other parts of the body.
You may have some treatments as part of a clinical trial.
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.