What are the aims of this leaflet?
This leaflet has been written to help you understand more about Linear IgA disease. It tells you what it is, what causes it, what can be done about it, and where you can find out more about it.
What is Linear IgA disease?
Linear IgA disease is a very rare blistering condition of the skin in adults. A similar condition affecting children is known as Chronic Bullous Disease of Childhood (CBDC).
The condition is called ‘Linear IgA disease’ because a type of protein called immunoglobulin A (IgA) can be seen deposited under the outer layer of the skin (the epidermis) in a line (linear) when a small sample of skin biopsy is prepared specially and examined under the microscope.
What causes Linear IgA disease?
Often no cause can be identified. Sometimes, infections and occasionally medicines may trigger linear IgA disease. The disease is thought to be related to the immune system (IgA protein) attacking structures in the skin layers (i.e. it is an autoimmune disease). When these structures are damaged, the skin blisters may form.
Is it hereditary?
What are the symptoms of Linear IgA disease?
These range from mild itching to a severe burning sensation.
What does it look like?
Patients have an itchy rash with small blisters, often arranged in clusters or rings. The blisters can come up all over the body and limbs, or just affect a few smaller patches. The blisters may show the ‘string of pearls sign’ which describes the presence of blisters lying around the rim of wheal-like red patches. Up to 80% of affected adults can have blisters or ulcers in the mouth, eyes or the genital region, but the internal organs remain clear.
In children, the rash often occurs in the genital region and on the face especially around the mouth.
How will it be diagnosed?
The diagnosis of Linear IgA can be difficult clinically and confirmation of the diagnosis requires a skin biopsy in which a line of IgA under the epidermis can be shown up by a special test (direct immunofluorescence).
Can it be cured?
Treatment suppresses Linear IgA disease but does not cure it. However, in the majority of patients the disease tends to eventually resolve. Skin lesions tend to heal without leaving permanent scars. However, ulcers in the eyes, mouth or genital region can leave scars or cause permanent damage.
How can it be treated?
Treatment choice depends on the severity of the disease. Most patients with linear IgA disease do well with tablets such as dapsone. Other medications such as sulphonamides, steroids, ciclosporin, mycophenolate mofetil and colchicine may be used. Oral antibiotics such as tetracyclines, or erythromycin have also been used.
Self care (What can I do)?
- Ask to see an eye specialist if you are getting problems with your eyes; for example, redness and a sore gritty feeling.
Where can I get more information about linear IgA disease?
Web links to detailed leaflets:
For details of source materials used please contact the Clinical Standards Unit (firstname.lastname@example.org).
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: individual patient circumstances may differ, which might alter both the advice and course of therapy given to you by your doctor.
This leaflet has been assessed for readability by the British Association of Dermatologists’ Patient Information Lay Review Panel
BRITISH ASSOCIATION OF DERMATOLOGISTS
PATIENT INFORMATION LEAFLET
PRODUCED SEPTEMBER 2004
UPDATED APRIL 2010, JULY 2013,
REVIEW DATE OCTOBER 2019