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Cutaneous Vasculitis


What are the aims of this leaflet?

This leaflet is written to help you understand more about cutaneous vasculitis. It tells you what it is, what causes it, what can be done about it and where to get more information about this condition.

What is cutaneous vasculitis?

Vasculitis is a term referring to inflammation of blood vessels.  These vessels may be arteries, veins or both, and vasculitis can affect any part of the body. When it affects small or medium sized blood vessels in the skin, it is known as cutaneous vasculitis. Occasionally cutaneous vasculitis can be a sign of inflammation occurring in other organs (a systemic vasculitis) and further investigation may be required for a full diagnosis.

What causes cutaneous vasculitis?

Cutaneous vasculitis may be caused by an infection, medications, autoimmune diseases, malignancy (cancer) or blood disorders. In about half of cases, no cause is found. The triggers can induce increased activity of the immune system (the body’s defence system), with increased production of inflammatory mediators which cause damage to blood vessel walls. Fluid may also leak from the blood vessels into the surrounding tissues which can result in swelling especially of the lower legs.


Vasculitis can occur 7-10 days after a viral or bacterial illness.

Autoimmune conditions:

Vasculitis may occur in patients with autoimmune diseases (where immune system reacts against patients own tissues) such as rheumatoid arthritis, lupus, and inflammatory bowel disease.


More than 100 drugs have been implicated in drug-induced vasculitis. These include antibiotics, anticonvulsants, diuretics, and non-steroidal anti-inflammatory agents. Any new medication taken will be the initial suspect of causing a vasculitic rash.

Malignancy or Haematological (blood) disorders:

Cancers may be associated with increased thickening of the blood or development of antibodies which can cause blood vessel damage. Abnormalities of the red or white blood cells can also lead to vasculitis.

Is vasculitis hereditary?

No, vasculitis is not known to be hereditary.

What are the features of cutaneous vasculitis?

The most common type of cutaneous vasculitis is cutaneous small vessel vasculitis (CSVV). This usually appears as non-blanching red or purple haemorrhage or bruise like marks on the skin, some of which may be raised lumps. These lesions are typically small, but may measure between 1 millimetre to several centimetres as rarely, pustules, blisters and wheals which heal with bruising may be seen. These often cause no symptoms but can sometimes cause pain, burning and itching. The ankles and lower legs as well as pressure points are most frequently affected.

If medium-sized vessels in the skin are affected, a network-like skin discolouration, ulceration or larger raised lesions may be seen.

Other symptoms to be aware of, which may suggest involvement of organs other than the skin include:

  • Fever

  • Nausea and vomiting

  • Blood in urine

  • Joint and muscle aches

  • Muscle weakness

  • Tingling or numbness in the hands and/or feet

  • Chest pain

  • Breathlessness or cough

  • Abdominal pain

  • Blood in the faeces

How is cutaneous vasculitis diagnosed?

The diagnosis can often be made based on the appearance of the skin.

  1. A skin biopsy usually confirms the diagnosis in classic cases. This is not always required.

  2. Blood tests are often carried out to check for the presence of infection, autoimmune and inflammatory conditions as well as haematological abnormalities.

  3. A urine sample, blood pressure check and blood tests are useful to exclude involvement of other organs.

  4. Very rarely, scans may be needed to check for vasculitis in other organs.

How can cutaneous vasculitis be treated?

Any underlying causes should be dealt with. For example, any possible drug culprits should be stopped (but only after advice by a doctor), and underlying infection should be treated.

Otherwise, initial treatment measures include:

  • Leg elevation

  • Adequate rest

  • Analgesics

  • Antihistamines

  • Non-steroidal anti-inflammatory drugs (except if there is kidney involvement)

  • Steroid creams and ointments applied to the skin

  • Dressings may be required if the skin is ulcerated

If the episode of vasculitis is prolonged, severe or leading to ulceration, oral medication such as the ones listed below may be required:

  • Colchicine

  • Dapsone

  • Oral corticosteroids

In patients with severe or systemic disease treatment with other drugs which suppress the immune system may be required.

Can cutaneous vasculitis be cured?

The outlook is good with a full recovery in 90% of cases (if only the skin is involved). The rash may recur at intervals for some time after the initial episode. Even after successful treatment, the areas affected by vasculitis can become more pigmented (brown or black) compared to non-affected skin. This discolouration usually takes months to fade to normal.

 Where can I get more information about vasculitis?

Web links to detailed leaflets:

Links to patient support groups:

For details of source materials used please contact the Clinical Standards Unit (

This leaflet aims to provide accurate information about the subject and is a consensus of the views held by representatives of the British Association of Dermatologists: its contents, however, may occasionally differ from the advice given to you by your doctor.

This leaflet has been assessed for readability by the British Association of Dermatologists’ Patient Information Lay Review Panel





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