Pemphigus vulgaris (PV) is a rare and serious condition that causes painful blisters to develop on the skin as well as inside the mouth, nose, throat, anus and genitals.
The blisters are fragile and can easily burst open leaving painful areas of raw, unhealed skin.
The blisters can fade and flare up later and it is impossible to predict how severe a flare-up might be.
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PV is what is known as an autoimmune condition. This means the immune system (the body’s defence against infection) malfunctions and starts attacking healthy tissue.
In cases of PV the immune system attacks cells found in a deep layer of skin as well as the cells found in the mucous membrane (the protective lining of the mouth, nostrils, throat, genitals and anus). This causes blisters to form in the affected tissue.
It is unclear why the immune system goes wrong in this way. PV could be caused by a combination of both genetic and environmental factors. What is known is that PV is not contagious and cannot be passed from one person to another.
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Treating pemphigus vulgaris
There is currently no cure for PV, although the symptoms respond well to high doses of steroid medication (.
Using a high dose of steroids over a long period of time can cause serious side effects. So when the symptoms have cleared, low doses are used in combination with other medicine. This is known as steroid-sparing therapy, and it prevents some of the dangerous side effects associated with long-term steroid use.
Recent research suggests that a type of medication called rituximab may be an effective treatment in severe cases that fail to respond to conventional treatment.
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A common complication of PV is the blisters becoming infected. In some cases infection can spread quickly into the blood (), affecting the whole body, which can be life-threatening.
Other complications include the side effects associated with steroid and immunosuppressant use.
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Who is affected
PV is a rare condition. Most cases first develop in older adults aged 50-60, although PV can affect people of all ages, including children. Both sexes are equally affected.
PV is slightly more common in people of Jewish, Indian and Mediterranean descent.
The outlook for people with PV has improved significantly since the introduction of steroids, although the complications associated with the condition can be life-threatening.
Most people with PV experience flare-ups when symptoms are particularly bad and then periods when they experience no or very few symptoms (this is known as remission). In some people the symptoms may go away permanently (complete remission).
Pemphigus vulgaris symptoms
Pemphigus vulgaris (PV) causes widespread blistering of the skin and mucous membranes, which line the mouth, nose, throat and genitals (the vagina, cervix, penis and anus).
These blisters can burst and turn into painful sores that can take some time to heal.
In most people with PV, blisters first appear in the mouth, and may later affect the skin. Blisters in the mouth turn into sores, making eating, drinking and brushing teeth very painful. If they spread to the larynx (voice box), the voice can become hoarse.
If the skin is affected, PV will cause delicate blisters to appear all over the skin. These blisters easily burst to reveal red sores. The sores can crust over and form scabs, which can eventually discolour the skin. Sores may join together to form large areas of raw-looking skin.
These symptoms will flare up at unpredictable times, and fade at other times.
Pemphigus vulgaris causes
Pemphigus vulgaris (PV) is an autoimmune condition. An autoimmune condition causes the body's immune system to attack its own cells and organs by mistake.
Normally, the immune system only responds like this to an invading germ or substance that it does not recognise, such as a virus or pollen.
In the case of PV, the immune system produces antibodies that damage the cells in the skin and mucous membranes (the lining of the mouth, nose, throat and genitals). The antibodies attack proteins called desmogleins, which hold the cells together. This causes the cells to fall apart. Fluid-filled blisters or sores then develop in the spaces.
It is not known why some people develop this reaction.
Is PV inherited?
PV is not passed down through families, and it is very unusual for more than one person in a family to have PV.
However, recent evidence suggests that the genes a person inherits from their parents, while not directly causing PV, may make them more susceptible to the disease.
Two genetic mutations (where the instructions found in all living cells become scrambled in some way) called DR4 and DRw4 are common in people with PV.
Most experts believe it also takes an external factor or combination of factors to trigger PV. This could be a bacterial or viral infection or something in the environment, such as a pollutant.
Diagnosing pemphigus vulgaris
Because pemphigus vulgaris (PV) is so rare, many doctors have not come across it before. If your doctor suspects PV, you will need to be referred to a dermatologist (skin specialist).
A dermatologist will confirm the diagnosis and prescribe appropriate treatment.
PV should always be suspected in anyone who has sores inside the mouth that do not heal. The mouth is affected in many cases of PV, and sores may also be seen in other places, such as the vagina or the skin.
Confirming the diagnosis
The diagnosis of PV can be confirmed by doing a skin, in which a sample of an unbroken blister is sent to a laboratory. The sample is examined under a microscope to see whether the skin cells are breaking apart, which would indicate PV.
To confirm the diagnosis further, a technique called immunofluorescence can be used.
- In direct immunofluorescence the skin biopsy is stained with dye to detect PV antibodies in the cells.
- In indirect immunofluorescence the levels of PV antibodies in the blood are measured.
Coping with a diagnosis
Being told you have a rare chronic disease can be a bewildering, frightening and sometimes lonely experience.
You may want to find out as much as you can about PV and how best to cope with it.
Treatment for pemphigus vulgaris
Treatment for pemphigus vulgaris (PV) usually involves taking a combination of two types of medication – steroid medication (oral corticosteroids) and immunosuppressants.
Both of these types of medication can prevent your immune system from damaging healthy tissue.
It can take a while to determine the best dose of these medications. There is often a fine balance to successfully controlling symptoms while limiting unpleasant side effects, so it may take some months until this balance can be achieved.
The aim of treatment is:
- To heal the blisters and prevent new ones from forming. It usually takes up to eight weeks for the blisters to heal and two to three weeks to prevent new ones from forming.
- To reduce the medication gradually to the lowest possible dose that will still control symptoms.
Oral corticosteroids (steroid tablets)
Corticosteroids are usually effective in reducing the harmful activity of the immune system in a short space of time.
They contain synthetic versions of hormones that can block some of the chemical reactions of the immune system. In blocking these reactions, further damage to the skin can usually be prevented.
When corticosteroids were first introduced as treatment for PV in the early 1950s, it led to a big fall in the number of deaths from the condition.
First stage: high dose
You usually start on a high dose of prednisolone (60-100mg a day). The dose will depend on how serious your condition is.
If you need more than 100mg a day, pulse therapy is an option. Pulse therapy involves you being given high doses of methylprednisolone plus cyclophosphamide through a drip in your arm.
Pulse therapy sessions are given three days a month for at least six months.
Some people notice an improvement in their symptoms within days of taking corticosteroids. On average, it takes two to three weeks for the blistering to stop.
Next stage: lowering the dose
Once your symptoms have been relieved, your medication is gradually reduced to the lowest possible dose that can still control your symptoms.
The lowest possible dose is used because corticosteroids have a wide range of unpleasant side effects, such as:
- weight gain
- mood changes, for example you may become aggressive, irritable and short tempered with people
- rapid mood swings, such as feeling very happy one minute and then very sad and weepy the next
Eventually, you may be able to come off corticosteroids altogether if your symptoms have disappeared and do not flare up when treatment is stopped. However, many people will always need to take a low dose of corticosteroids to keep symptoms under control.
Long-term corticosteroid use does increase the risk of you developing a range of health conditions, such as:
- weakening of the bones ( )
- the onset of , or worsening of existing diabetes
Read more aboutincluding how they work and their possible side effects.
As their name suggests, immunosuppressants suppress or ‘dampen down’ the immune system.
By combining them with corticosteroids it is often possible to reduce the dosage of your steroid medication, meaning you are less likely to experience side effects and long-term complications such as osteoporosis. This is known as steroid-sparing therapy.
The most commonly used immunosuppressants in the treatment of PV include:
- mycophenolate mofetil
These medications are usually taken in tablet form. If one immunosuppressant does not seem to be effective then another one can be tried.
Immunosuppressants can make you more vulnerable to infection so you will need to take precautions when taking them, such as:
- avoiding close contact with someone known to have an active infection, especially if it is or , as the virus that causes these two infections could make you feel very ill
- if possible avoiding crowded places
- reporting any possible symptom of infection, such as a high temperature or swelling, immediately to your doctor or dermatologist
In addition, azathioprine can make your skin more vulnerable to the effects of sunlight so you should wear sunscreen on bright days.
Immunosuppressants are not suitable for pregnant women as they can cause birth defects. If you are a sexually active woman you should use a reliable method of contraception while taking immunosuppressants.
There are several other treatments that are sometimes used in combination with corticosteroids and immunosuppressants.
- dapsone – a type of medication that can help prevent blisters from becoming infected with bacteria
- colchicine – which is a medication that can reduce levels of inflammation in the body and can help prevent new blisters from forming
- tetracycline – a type of antibiotic that, like dapsone, can be useful in preventing infections
Rituximab is a new type of medication that works by targeting what are known as B cells. These are a type of white blood cell that the immune system uses to attack healthy skin tissue in cases of PV.
Research published in 2011 concluded that rituximab is an effective alternative to conventional treatment in cases where it is ineffective or causes serious side effects.
Rituximab is administered directly into your vein over the course of a few hours.
It is still unclear what the most effective method of prescribing rituximab is. Some doctors have tried using it once a week over the course of four weeks.
Others have suggested it should be used six times over the course of two months followed by four more doses once a month. Further research is needed.
It is common to experience flu-like symptoms when you are being treated with rituximab. Possible symptoms include:
- fever or chills
- muscle pain
You may be given additional medication to prevent or lessen side effects, although the side effects should improve as your body gets used to rituximab.
Current evidence suggests that around 1 in 14 people will experience more serious side effects after taking rituximab, typically an infection such as pneumonia or sepsis (infection of the blood or 'blood poisoning’).
A practical disadvantage of rituximab is that it is a relatively expensive medication and some primary care trusts may be unwilling to fund treatment.
If you think you could benefit from rituximab you should discuss the issue with your dermatologist.
Complications of pemphigus vulgaris
Secondary infections are a common complication of pemphigus vulgaris (PV).
The blisters caused by PV are vulnerable to bacterial infection and this is made worse as most of the medications used to treat PV weaken the immune system.
Symptoms of an infected blister include:
- the blister or surrounding skin becomes more painful and hot
- the blister is filled with yellow or green pus
- there are red streaks leading away from the blister
It's important not to ignore an infected blister as it could potentially lead to(a contagious bacterial infection of the skin) if it splits open (ruptures).
This could lead to further complications such as cellulitis](/health-library/conditions/cellulitis) (a bacterial infection of the deeper layers of the skin) or [sepsis (a life-threatening infection of the blood).
Contact your doctor or dermatologist if you think you may have an infected blister.
An infected blister can be treated with antibiotics.
Long-term corticosteroid use
If you are required to take steroid medication (corticosteroids) on a long-term basis (more than three months) the side effects include:
- further weight gain
- thinning skin that can bruise easily
- muscle weakness
- a combination of fatty deposits that develop in the face (moon face), stretch marks across the body and acne – this is known as
- weakening of the bones ( )
- the onset of , or worsening of existing diabetes
- – an eye condition where fluid gathers inside the eye
- – an eye condition where cloudy patches develop at the front of the eye
- delayed wound healing
- increased risk of infection
These side effects should improve if you're able to reduce your dosage. However, osteoporosis can be a persistent problem, particularly if you are over 65. This can make you more vulnerable to breaking a bone.
Your doctor can prescribe medication, calcium and vitamin D supplements, which help strengthen your bones and can compensate for the effects of prednisolone. Find out more about.
You may also be referred for a type of X-ray called a dual energy X-ray absorptiometry (DEXA) scan. This can be used to assess how strong your bones are. Seefor more information.
Stomach ulcers can also be a problem for people who take high doses of oral corticosteroids on a long-term basis. To protect against stomach ulcers, you may be prescribed a type of medication called a proton pump inhibitor (PPI). This reduces the amount of acid in your stomach, which will make you less vulnerable to developing stomach ulcers. Find out more about.
You will also probably have regular checks and tests for conditions such as diabetes, high blood pressure and glaucoma if you need to take oral corticosteroids on a long-term basis.
Immunosuppressants and cancer
There is evidence that taking an immunosuppressant on a long-term basis increases your risk of developing cancer, particularly.
One study looked at people who were taking immunosuppressants to prevent their body from rejecting a kidney transplant.
The study found that just over half of these people developed cancer, typically 15 years after they began treatment.
It is unclear whether a similar risk exists in cases of PV and it may well be the case that you are not required to take an immunosuppressant for 15 years or more.
But as a precaution it is recommended that:
- you quit smoking if you smoke
- you avoid exposing your skin to too much sunlight
- you never use sunbeds or sun lamps