Introduction

Behçet's disease, or Behçet's syndrome, is a rare and poorly understood condition that results in inflammation of the blood vessels and tissues.

Confirming a diagnosis of Behçet's disease can be difficult because the symptoms are so wide-ranging and general (they can be shared with a number of other conditions).

This page covers:

Symptoms of Behçet's disease

The main symptoms of Behçet's disease include:

In severe cases, there's also a risk of serious and potentially life-threatening problems, such as permanent vision loss and strokes.

Most people with the condition experience episodes where their symptoms are severe (flare-ups or relapses), followed by periods where the symptoms disappear (remission).

Over time, some of the symptoms can settle down and become less troublesome, although they may never resolve completely.

Read about the symptoms of Behçet's disease.

Diagnosing Behçet's disease

There's no definitive test that can be used to diagnose Behçet's disease.

Several tests may be necessary to check for signs of the condition, or to help rule out other causes, including:

Current guidelines state a diagnosis of Behçet's disease can usually be confidently made if you've experienced at least three episodes of mouth ulcers over the past 12 months and you have at least two of the following symptoms:

  • genital ulcers
  • eye inflammation
  • skin lesions (any unusual growths or abnormalities that develop on the skin)
  • pathergy (hypersensitive skin)

Other potential causes also need to be ruled out before the diagnosis is made.

Causes of Behçet's disease

The cause of Behçet's disease is unknown, although most experts believe it's an autoinflammatory condition.

An autoinflammatory condition is where the immune system – the body's natural defence against infection and illness – mistakenly attacks healthy tissue.

In cases of Behçet's disease, it's thought the immune system mistakenly attacks the blood vessels.

It's not clear what triggers this problem with the immune system, but two things are thought to play a role:

  • genes – Behçet's disease tends to be much more common in certain ethnic groups where the genes that are linked to the condition may be more common
  • environmental factors – although a specific environmental factor hasn't been identified, rates of Behçet's disease are lower in people from an at-risk ethnic group who live outside their native country

Behçet's disease is more common in the Far East, the Middle East and Mediterranean countries such as Turkey, Iran and Israel.

People of Mediterranean, Middle Eastern and Asian origin are thought to be most likely to develop the condition, although it can affect all ethnic groups.

Treating Behçet's disease

There's no cure for Behçet's disease, but it's often possible to control the symptoms with medicines that reduce inflammation in the affected parts of the body.

These medications include:

  • corticosteroids – powerful anti-inflammatory medications
  • immunosuppressants – medications that reduce the activity of the immune system
  • biological therapies – medications that target the biological processes involved in the process of inflammation

Your healthcare team will create a specific treatment plan for you depending on your symptoms.

Read about treating Behçet's disease.

Specialist Behçet's disease centres

There are three NHS Centres of Excellence that have been set up to help diagnose and treat people with Behçet's disease. These are located in London, Birmingham and Liverpool. Residents of Wales may access these centres but first need the approval of their local Health Board to do so.

You may be referred to one of these centres so a diagnosis can be confirmed. Staff at these centres may also liaise with specialists at other centres to help with a person's management and treatment, even if they're not seen directly.

You can find out more about these centres on the Behçet's Syndrome Centres of Excellence website.

If you have a child affected by Behcet's disease then clinicians may pass that information onto the Congenital Anomaly Register and Information Service for Wales (CARIS), after they have provided you with information about CARIS. CARIS is part of the NHS in Wales and aims to help NHS staff plan more effectively to help people affected by a congenital anomaly or rare disease. Find out more information about the CARIS register.

This helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.

Find out more about the register.

Further information about Behçet's disease

A natural response to receiving a diagnosis of a complex condition such as Behçet's disease is to find out as much as possible about the condition.

However, in the UK this may be difficult because Behçet's disease is so rare that even most healthcare professionals know little or nothing about it.

A good place to start to learn more about Behçet's disease is the Behçet's Syndrome Society (BSS). The BSS is the UK's main patient support group for people with Behçet's disease.

The BSS website has a range of information about different aspects of Behçet's disease, a member's forum, blogs, and links to other useful resources.

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Symptoms

Behçet's disease can cause a wide range of symptoms, but it's rare for someone with the condition to have all of them at once.

Most people experience times when the symptoms improve (remission) and times when they get worse (flare-ups or relapses).

The main symptoms of Behçet's disease are outlined below.

Mouth ulcers

Almost everyone with Behçet's disease develops mouth ulcers. The ulcers look the same as normal mouth ulcers, but can be more numerous and painful. They most often develop on the tongue, lips, gums and the insides of the cheeks.

The ulcers usually heal within a couple of weeks without leaving any scarring, although they'll often return.

Genital ulcers

Like mouth ulcers, recurrent genital ulcers are also a common symptom of Behçet's disease.

In men, the ulcers usually appear on the scrotum. In women, they usually appear on the cervix (neck of the womb), vulva or vagina. However, genital ulcers can appear anywhere in the groin area, including on the penis.

The genital ulcers are usually painful and leave scarring in around half of all cases. Men may also experience inflammation (swelling) of the testicles and women may find the ulcers make having sex painful.

Genital ulcers caused by Behçet's disease are not contagious and can't be spread through sexual intercourse.

Skin lesions

Many people with Behçet's disease also develop skin lesions. A lesion is any type of unusual growth or abnormality that develops on your skin, such as a bump or a discoloured area of skin.

Skin lesions that can occur in Behçet's disease include red, tender swellings on the legs called erythema nodosum and more widespread acne-like spots called pseudofolliculitis.

Skin lesions often heal within 14 days, although they may come back frequently. Erythema nodosum lesions may leave permanently discoloured areas of skin.

Inflammation of the joints

Behçet's disease affects the joints in up to two in every three people with the condition, causing arthritis-like symptoms such as pain, stiffness, swelling, warmth and tenderness.

The joints most often affected include the knees, ankles, wrists and small joints in the hands.

Unlike some conditions affecting the joints, permanent joint damage is rare in Behçet's disease and symptoms can usually be controlled successfully.

Inflammation of the eyes

Inflammation of the eyes is another common symptom of Behçet's disease, occurring in around half of all cases. It often develops very suddenly.

Inflammation often affects the uveal tract, which is a group of connected structures inside the eye. Sometimes both eyes may be affected at the same time.

Inflammation of the uveal tract is known as uveitis and it can cause symptoms that include:

  • painful red eyes
  • floaters (dots that move across the field of vision)
  • blurred vision

In the most severe cases of Behçet's disease, inflammation of the eyes can lead to permanent loss of vision. However, this is far less likely with early and appropriate treatment.

Sensitive skin

In some people with Behçet's disease, the skin is particularly sensitive to injury or irritation. This is known as pathergy.

For example, if a needle is used to prick the skin of someone who has pathergy, a large red bump would develop within a day or two that appears out of proportion to the original needle prick.

Gastrointestinal symptoms

Behçet's disease can cause inflammation of the stomach and bowel, which can lead to symptoms such as:

Occasionally, the inflammation can cause the bowel to become damaged and bleed. Having blood in your stools is a possible symptom of inflammation of the internal lining of the bowel.

Blood clots

The inflammation of the lining of the blood vessels associated with Behçet's disease can sometimes cause blood clots to form.

One of the most common types of blood clot to affect people with Behçet's disease is deep vein thrombosis (DVT), where a blood clot develops in one of the deep veins of the body, usually in the legs.

Symptoms of DVT include:

  • pain, swelling and tenderness in one of your legs (usually in the calf)
  • a heavy ache in the affected area
  • warm skin in the area of the clot
  • redness of your skin, particularly at the back of your leg below the knee

DVT often requires immediate medical treatment. If you suspect DVT,  go to your nearest accident and emergency (A&E) department immediately.

In people with Behçet's disease, careful assessment is needed to determine if it's safe to use blood thinning treatment for this complication. Treatment to control inflammation is usually more effective.

Cerebral venous thrombosis

A less common type of blood clot associated with Behçet's disease is cerebral venous thrombosis (CVT). This occurs when a blood clot develops inside the blood vessels that run through channels located between the outer and inner layer of your brain.

The blood clot can increase the pressure inside your skull and also lead to an interruption of the blood supply to the brain (stroke).

Symptoms of a CVT include:

  • a severe headache – this has been described as a throbbing, piercing, band of pain, or as a very severe pain that suddenly appears out of nowhere
  • slurred speech
  • seizures (fits)
  • hearing loss
  • double vision
  • stroke-like symptoms, such as muscle weakness or paralysis – but, unlike most strokes, both sides of the body can be affected

CVT should be regarded as a medical emergency. If you suspect a stroke, dial 999 immediately to request an ambulance.

Aneurysms

Inflammation of the blood vessels can cause the walls of your blood vessels to weaken. This causes the walls to bulge outwards as a result of blood pressure. The bulge is known as an aneurysm.

Aneurysms don't usually cause any noticeable symptoms unless the wall of the blood vessel becomes so weak that it enlarges or ruptures. This can place pressure on nearby areas and can sometimes lead to internal bleeding or organ dysfunction.

The symptoms of a ruptured aneurysm can vary depending on where in the body the aneurysm developed. Possible symptoms include:

Inflammation of the nervous system

Inflammation of the central nervous system (CNS) causes the most serious symptoms associated with Behçet's disease.

The symptoms of CNS inflammation usually develop quickly over the space of a few days, and can include:

  • headache
  • double vision
  • loss of balance
  • seizures (fits)
  • partial paralysis on one side of the body
  • behavioural or personality changes

General symptoms

It's also common for people with Behçet's disease to experience more general symptoms as a result of the condition, including periods of extreme physical or mental tiredness (fatigue). This can affect a person's ability to perform any sort of activity.

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Treatment

There's currently no cure for Behçet's disease, but a number of treatments can help to relieve symptoms and reduce the risk of serious complications.

Once a diagnosis of Behçet's disease has been confirmed, you'll usually be referred to several different specialists who have experience of treating the condition. They'll help draw up a specific treatment plan for you.

The specialists involved in your care may include:

  • a dermatologist – a doctor who specialises in treating skin conditions
  • an oral medicine specialist – a doctor or dentist who specialises in conditions affecting the mouth
  • a rheumatologist – a doctor who specialises in treating joint conditions and conditions affecting the entire body
  • an ophthalmologist – a doctor who specialises in treating eye conditions
  • a neurologist – a doctor who specialises in treating conditions that affect the nervous system and brain

You may see more than one specialist during the same visit to hospital, to help with diagnosis and creating a treatment plan.

Your treatment plan usually involves the use of a combination of different medications. Depending on the type and severity of your symptoms, you may only need to take medication when you have a flare-up.

Alternatively, you may have to take medication on a long-term basis to stop serious complications developing, such as vision loss.

Medications

A number of different medications can be used to treat the various symptoms of Behçet's disease, but the main types of medication used can be broadly divided into:

  • corticosteroids
  • immunosuppressants
  • biological therapies

Corticosteroids

Corticosteroids are powerful anti-inflammatory medications that can be useful in reducing the inflammation associated with Behçet's disease.

Depending on the specific symptoms being treated, corticosteroids are available as:

  • topical corticosteroids – applied directly to the area affected as eye drops, creams or gels
  • oral corticosteroids – these reduce inflammation throughout the body and come as tablets or capsules

Occasionally, corticosteroid injections may also be used.

Side effects depend on the form of corticosteroid you are taking. Side effects associated with topical corticosteroids are uncommon, but long-term use may lead to problems such as a thinning of your skin.

The long-term use of oral corticosteroids is associated with some potentially more serious side effects, including:

Immunosuppressants

Immunosuppressants are a type of medication that reduces the activity of the immune system, which in turn interrupts the inflammation process that causes most of the symptoms of Behçet’s disease.

Examples of immunosuppressants used to treat Behçet's disease include azathioprine, ciclosporine, methotrexate, mycophenolate mofetil and thalidomide.

These medications are usually available as tablets, capsules and injections. Colchicine, an anti-inflammatory medication often used for gout, may also be beneficial.

While immunosuppressants can be useful in treating a wide range of Behçet's disease symptoms, they can also cause some potentially significant side effects.

For this reason, you'll be given careful advice about potential side effects and monitoring through blood tests. This is often co-ordinated by a specialist nurse.

General side effects of these medications can include:

  • effects on blood cells and liver function (regular monitoring of blood tests may be required)
  • increased risk of infections – you should report any symptoms of a possible infection to your GP or healthcare team as soon as possible
  • feeling sick and vomiting
  • abdominal (tummy) pain
  • diarrhoea
  • hair loss, which is usually temporary
  • pins and needles
  • muscle cramps and weakness

Some immunosuppressants can also cause birth defects and shouldn't be taken if you're pregnant or planning a pregnancy.

If you're taking any of these medications, you should ensure you talk to your specialist or GP about the possible effects of your medication on a potential pregnancy.

Biological therapies

Biological therapies are a newer type of medication that target the biological processes involved in the process of inflammation more selectively.

For example, one group of medications called tumour necrosis factor alpha inhibitors (TNFa-inhibitors) work by targeting the antibodies thought to cause much of the inflammation associated with Behçet's disease.

Biological therapies used to treat Behçet's disease include infliximab and interferon alpha. These may either be given directly into a vein (intravenously) or by injection under the skin (subcutaneous injection) at varying intervals.

While they're often effective, biological therapies are also very expensive. Your local hospital will usually only agree to fund biological therapies on the NHS if your symptoms are severe and other medications haven't been effective.

Biological therapies can also cause a range of side effects, including:

As with immunosuppressant treatment, you should report any symptoms of a possible infection to your GP or healthcare team as soon as possible.

Treating specific symptoms

The specific medications used for Behçet's disease vary depending on the symptom being treated. The treatments for some of the main symptoms associated with the condition are outlined below.

Ulcers and skin lesions

Topical corticosteroids – such as creams, lozenges, mouthwashes and sprays – are usually the first treatment recommended for mouth and genital ulcers.

Some people find that using a corticosteroid inhaler is effective. These inhalers are commonly used to treat asthma and are normally used to spray the medication into the lungs. However, rather than inhaling the steroids, you can use the inhaler to spray the steroids directly on to an ulcer.

If you have red, tender swellings on your legs (erythema nodosum), you may be prescribed colchicine tablets to reduce the inflammation of your skin.

For severe ulcers and lesions that don't respond to other treatments, other immunosuppressant tablets or biological therapies may be recommended.

Eye inflammation

Because of the potential risk of vision loss in serious cases, any eye inflammation caused by Behçet's disease should be carefully monitored by an ophthalmologist.

Treatment for eye problems often involves taking azathioprine and corticosteroid tablets, although corticosteroid eye drops may also be useful.

In severe cases where these treatments haven't helped, mycophenolate mofetil, ciclosporine or biological therapies may also be recommended.

Joint pain

For people with joint pain caused by Behçet's disease, conventional painkillers such as paracetamol and non-steroidal anti-inflammatory drugs (NSAIDs) may sometimes help relieve the pain.

Daily colchicine tablets can also help by reducing the inflammation in your joints.

In severe cases where these treatments haven't helped, azathioprine or biological therapies may be recommended.

Gastrointestinal symptoms

A number of different medications may be used to help reduce inflammation of the stomach and bowel caused by Behçet's disease, including corticosteroids, immunosuppressants and biological therapies.

Sometimes the inflammation in your bowel causes it to become damaged and bleed. Medical treatment is usually successful, though rarely emergency surgery may be needed to stop the bleeding and remove the affected section of bowel.

Headaches

In cases of Behçet's disease, headaches are usually treated in the same way as migraines. This means there are two types of medication that can be used:

  • medication to prevent the symptoms of a headache occurring, such as beta-blockers
  • medication to help relieve the headache, such as NSAIDs and a type of medication called triptans

Read more about treating migraine and preventing migraine.

Blood clots

It's not entirely clear whether blood clots associated with Behçet's disease should be treated in the same way as blood clots caused by other conditions, or whether using medication to treat the underlying inflammation is more appropriate.

Normally, blood clots are treated with a type of medication called an anticoagulant, which helps thin the blood and reduces the risk of the blood clot blocking the flow of blood.

However, the use of anticoagulants for Behçet's disease is controversial because the blood clots are slightly different to other clots – they tend to stick to the side of the blood vessel walls, rather than break off and travel through the bloodstream.

Using anticoagulants in Behçet's disease could also potentially increase the risk of any aneurysms rupturing and causing serious internal bleeding.

Blood clots are often treated with a combination of corticosteroid or immunosuppressant tablets to reduce the inflammation in the blood vessels. Anticoagulants are only used if you've been screened to make sure there are no aneurysms.

Aneurysms

Aneurysms caused by Behçet's disease are normally treated with a combination of corticosteroid and immunosuppressant tablets, or infusions of cyclophosphamide to reduce inflammation in the affected blood vessel and stop the aneurysm getting worse.

Surgery or procedures may also be considered. The aneurysm may be repaired or bypassed using small tubes called stents, or it can be blocked off. This is often combined with medical treatment to reduce or prevent the risk of recurrence.

For more information about how surgery is used to treat some common types of aneurysm, see treating brain aneurysms and treating abdominal aortic aneurysms.

Central nervous system inflammation

Relatively minor symptoms of central nervous system inflammation, such as double vision, may get better on their own without the need for treatment.

However, more serious symptoms, such as paralysis and behavioural changes, usually require treatment with medication. This will often be in the form of corticosteroid or immunosuppressant injections, or biological therapies.

Pregnancy and fertility

Fertility is usually unaffected in women with Behçet's disease, but it's important that any pregnancy is planned where possible. This is because many of the medications used to treat the condition, such as thalidomide, can cause birth defects.

It's recommended that you use at least one reliable method of contraception until you decide that you want to have a baby. You should discuss your plans to have a baby with your care team, who will be able to adjust your treatment plan to make your pregnancy as safe as possible.

There's little evidence that having Behçet's disease increases your risk of pregnancy-related complications, although there's a very small chance of your baby being born with a temporary condition called neonatal Behçet's disease.

The fertility of men with Behçet's disease may be affected. This can be the result of the condition itself or of a side effect of some of the immunosuppressant medications. Colchicine may temporarily lower sperm count, but this often improves when treatment is stopped.

Where fertility is affected, further investigation – and, in some cases, fertility treatment such as in vitro fertilisation (IVF) – may be needed to conceive successfully.

Read more about treating infertility.

Neonatal Behçet's disease

There's a possibility that a baby can be born with a type of Behçet's disease that can cause ulcers on the baby's genitals and mouth. This type of Behçet's disease, known as neonatal Behçet's disease, is extremely rare, with only one or two cases being reported every few years.

Corticosteroids can be used to help relieve symptoms of neonatal Behçet's disease. The condition usually resolves within six to eight weeks of the birth.

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The information on this page has been adapted by NHS Wales from original content supplied by NHS Choices.
Last Updated: 16/06/2017 12:55:31