Mastocytosis and Mast Cell Disorders
A mast cell is a type of white blood cell. Mastocytosis is a condition in which there are too many mast cells in the body, Another disorder involves a normal number of mast cells, but they are more active than normal.
What sort of mast cell disorders are there?
You've basically got three main types:
- Mastocytosis - there are too many cells.
- Mast cell activation syndrome - there are normal numbers of cells but they zap around like hyperactive 2-year-olds. It's also sometimes called mast cell activation disorder.
- Localised mast cell disorder - for reasons best known to themselves the mast cells hang around together in one place, drinking cider and making a general nuisance of themselves.
Who gets these disorders?
Anyone really, but it's pretty rare. It's seen in about 1 in 150,000 people. The skin type is mostly seen in kids. It can affect males and females equally.
What are the symptoms?
It depends on the type.
Cutaneous means skin. One of the most common skin problems caused by mastocytosis is urticaria pigmentosa. It starts in babies but can go on into the teens. It causes a rash anywhere on the body that looks like light brown, itchy raised patches. It can be associated with other allergy problems like anaphylaxis (a severe allergy reaction) and skin writing (dermographism). A less common skin condition is called diffuse cutaneous mastocytosis which looks like a very itchy rash with yellow skin. Large blisters can develop for no reason.
A red, brown or yellow lump can develop on the skin. This is called a mastocytoma. Very unusually, one of these lumps can be cancerous.
Systemic is the word used in medicine to mean a generalised condition affecting most or all of the body. Symptoms depend on which parts of the body are involved. Common features include skin problems, tummy conditions, and disorders of the lungs and bones.
Read more about the symptoms of mastocytosis and mast cell disorders.
What causes these disorders?
If I knew that I'd be writing this leaflet on a beach in the Bahamas rather than a patio in North London. It's thought to be inherited (a fault in genetic material), which means there's another thing you can thank your parents for.
It's known that symptoms can be triggered by a variety of factors, including temperature changes, rubbing, stress, foods, insect bites and various infections.
Learn more about the causes of mastocytosis and mast cell disorders.
How are they diagnosed?
A doctor may be able to guess the diagnosis of the cutaneous type from the appearance of your skin. However, many different conditions can produce similar symptoms, such as liver and bowel conditions, glandular disorders and rare tumours. Other skin complaints can also produce similar rashes. You're likely to need blood and urine tests, X-rays or scans and samples (biopsies) taken from your skin and bone marrow (the jelly-like substance inside your bones).
Find out more about the diagnosis of mastocytosis and mast cell disorders.
What treatment is available?
There are no wonder cures, but lots of medicines are available to help control symptoms. If you develop severe allergy reactions (anaphylaxis) you might have to carry one of these adrenaline (epinephrine) pens. Don't keep it in the same pocket as your e-cigarette or you'll be in for a big surprise. The good news is you'll be justified in wearing one of those cool medical emergency identification bracelets or similar.
Medicines are available for skin problems, disorders of your digestive system and wheezing. If the condition gets serious, there's some pretty heavy stuff available, including surgical removal of the spleen, bone marrow transplant and stem cell therapy.
Read more about the treatment of mastocytosis and mast cell disorders.
What is the outlook?
In most cases the condition either settles down or you get a few symptoms over the years that can be controlled by medication. The localised form just causes lumps that don't do very much but in rare cases they behave like little cancer tumours and invade the surrounding tissues. Occasionally, an aggressive form of the systemic condition can be life-limiting.
Learn more about the outlook (prognosis) of mastocytosis and mast cell disorders,
What are mast cells?
Mast cells are a type of white blood cell. They are packed with histamine, a chemical released when you get an allergic reaction, and heparin, a chemical which stops the blood from clotting. Mast cells are hard-working cells that have many functions, including helping to fight infection and healing wounds.
However, mast cell disorders can occur in which too many cells are produced or they become overactive.
What are the types of mast cell disorder?
This is the term used when too many mast cells are produced. There are many different types of mastocytosis and it would be confusing to list them all. The types you are most likely to come across are:
- Those involving the skin (cutaneous).
- Those which involve lots of different tissues of the body (systemic).
Much less commonly there is a localised type in which clumps of mast cells gather in one place.
Mast cell activation syndrome
You may also see mast cell activation syndrome (MCAS) called mast cell activation disorder (MCAD). The mast cells are present in normal numbers but they are triggered to release their chemicals more readily than usual. The symptoms are generally the same as mastocytosis.
Localised mast cell disorder
Rarely, clumps of mast cells can develop in one area of the body.
Who gets a mast cell disorder?
These conditions are not very common. It occurs in about 1 in 150,000 people. The most common type - urticaria pigmentosa (see Symptoms, below) - is seen in 1 person in every 1,000 who attends a skin (dermatology) clinic.
What are the symptoms of mast cell disorders?
When larger than normal numbers of mast cells are present in the skin they commonly cause a condition called urticaria pigmentosa. Another less common condition called diffuse cutaneous mastocytosis is also sometimes seen.
By James Heilman, MD (Own work) [CC BY-SA 3.0 (http://creativecommons.org/licenses/by-sa/3.0)], via Wikimedia Commons
- This usually starts in babies a few months old but can go on for years. It causes a rash to appear anywhere on the body made of light brown, itchy raised patches.
- If you rub the patches, they become red and swollen and blisters develop. This is called Darier's sign.
- Rarely, after rubbing or applying heat to the skin, a severe allergic effect (an anaphylactic reaction) can occur .
- Your child may develop dermographism - this is a condition in which you can 'write' on the skin with a blunt object.
- The condition usually gets better as your child gets older and usually disappears by the time they reach their teens. Rarely, an adult form can develop.
Diffuse cutaneous mastocytosis
- This usually occurs in children less than 1 year old.
- They develop a very itchy rash with yellow, thickened skin.
- Large blisters can appear for no reason or after a very light amount of rubbing.
- If large areas of skin are involved, bodily symptoms can develop such as flushing, headache and the sensation of having a 'thumping' heart (palpitations). Tummy pains, diarrhoea and breathlessness can occur., The child can go into shock and become very ill. Some children have died of this condition.
Rarely, clumps of mast cells can form a nodule in the skin, which is usually red, brown or yellow in colour. This is called a mastocytoma. Even more rarely, a cancerous lump called a mast cell sarcoma can develop.
This can cause a whole range of symptoms depending on the parts of the body where large numbers of mast cells are found. For example:
- Skin - flushing of the face, urticaria pigmentosa (see above).
- Digestive system - tummy pains, diarrhoea, pale stools that are difficult to flush, feeling sick (nausea) or being sick (vomiting), acid indigestion, stomach ulcers.
- Swelling of the liver or spleen.
- Circulatory problems - fainting, low blood pressure, anaphylactic shock.
- Anaemia; other problems with the blood or bone marrow.
- Fractures of the bones (because of bone marrow involvement).
- Swollen lymph nodes.
- Breathing difficulties.
- Headaches, pins and needles, numbness.
What causes mast cell disorders?
The cause is not known. It is suspected that there is a fault in the gene (the material inherited from your parents) that controls mast cell production.
Triggers for mastocytosis symptoms
Although not strictly speaking the cause of mastocytosis, a number of factors are known to trigger the symptoms. These include:
- Physical triggers - for example, heat, cold, rubbing, sunlight, tiredness, lots of exercise, a high temperature (fever).
- Emotional triggers - for example, stress.
- Some foods - for example, cheese, spices, shellfish, food preservatives, flavourings and colourings, monosodium glutamate.
- Toxic substances in the environment - for example, perfumes, pesticides.
- Insect bites, jelly fish stings, snake bites.
- Infection with germs (bacteria), funguses or viruses.
- Medicines - for example, anaesthetic agents, aspirin, antibiotics, opioids, and many other medications.
How are these conditions diagnosed?
It's usually possible to guess the diagnosis if the skin is involved. However, the more generalised form causes so many different symptoms it may only become clear what the problem is once tests have been done.
What else could it be?
Because there can be so many different symptoms, the disorders can easily be confused with other conditions. These can include other skin disorders, liver and bowel problems, glandular conditions and rare tumours.
Will I need any tests?
You will need a sample taken from your skin (a biopsy) for genetic testing. Chest and bone X-rays or scans may be needed. Various blood and urine tests will be arranged. The main test involves removing some bone marrow or tissue from an area other than the skin. The sample is tested for the presence of mast cells: various genetic and chemical tests may also be performed.
How are mastocytosis and other mast cell disorders treated?
There is no treatment that will actually cure these conditions but a wide variety of medicines is available to control the symptoms.
If you're prone to sudden severe allergy symptoms you should avoid trigger factors. It's a good idea to wear a medical emergency identification bracelet or similar. If you've been given treatment advice from a specialist about what to do during an attack, carry it with you. Acute severe reactions are usually treated with adrenaline (epinephrine) injections, anti-allergy medication, fluids into a vein and steroids. You might need to carry an adrenaline (epinephrine) pen injector with you which can be obtained from your doctor. Some people need a course of injections to reduce their sensitivity to insect stings.
Skin and symptoms related to blood circulation
- Itching, flushing and other skin allergy symptoms can be controlled by medicines called H1-receptor and H2-receptor antagonists. These include chlorphenamine, ketotifen and cimetidine.
- Medication which stabilises the mast cells such as sodium cromoglicate, nedocromil and ketotifen.
- Steroid creams or ointments and injections are sometimes used.
- Treatment also used for psoriasis - called psoralen combined with ultraviolet A (PUVA) treatment - sometimes helps.
Inhalers to relax the airways - for example, salbutamol - can be helpful.
- H2-receptor antagonists or proton pump inhibitors help to control the effects of excess acid.
- Oral sodium cromoglicate is beneficial in people with diarrhoea and tummy (abdominal) pain.
- Anticholinergic medication such as propantheline (which blocks the effects of a body chemical called acetylcholine) may help control diarrhoea.
Medicines called leukotriene inhibitors used mainly in asthma - for example, montelukast - have been used. Low-dose aspirin and steroid tablets have been found helpful to control many different symptoms.
If the condition is severe, surgery to remove the spleen (splenectomy), medicines that have an effect on the immune system (such as interferon), bone marrow transplant or stem cell therapy may be considered.
What is the outlook for these conditions?
Cutaneous mastocytosis in children often settles down with time. Adults can go on to develop the systemic form.
Systemic mastocytosis tends to be persistent and the outlook (prognosis) depends on which parts of the body are involved. In most cases, it just keeps going at a low level for decades, requiring symptomatic treatment. Occasionally, however, it can become aggressive and even life-threatening.
Most cases of localised mastocytosis cause lumps that are nothing to worry about but occasionally cancers do occur which invade the surrounding tissue.
Further reading & references
- Cardet JC, Akin C, Lee MJ; Mastocytosis: update on pharmacotherapy and future directions. Expert Opin Pharmacother. 2013 Oct;14(15):2033-45. doi: 10.1517/14656566.2013.824424.
- Maculopapular cutaneous mastocytosis; DermNet NZ, 2014
- Pardanani A; Systemic mastocytosis in adults: 2017 update on diagnosis, risk stratification and management. Am J Hematol. 2016 Nov;91(11):1146-1159. doi: 10.1002/ajh.24553.
Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. Patient Platform Limited has used all reasonable care in compiling the information but makes no warranty as to its accuracy. Consult a doctor or other healthcare professional for diagnosis and treatment of medical conditions. For details see our conditions.
Dr Laurence Knott
Dr John Cox