chronic bullous disease of childhood

 

This is a rare autoimmune skin condition which results in clusters of blisters developing in rings often on the face or genitals. In autoimmune disorders, antibodies – which usually seek and destroy foreign invaders to the body, such as viruses – attack the body’s own cells instead. This causes inflammation and damage. Other autoimmune disorders include some types of arthritis and inflammatory bowel disease.

 

 

Chronic bullous disease of childhood is also known as chronic bullous dermatosis or linear IgA dermatosis of childhood. There is a similar condition called IgA dermatosis which affects adults but its development and treatment are different from that in children

The main feature is the development of clusters of blisters in specific areas of the body. These blisters are usually itchy and uncomfortable. Some children have many of these clusters, others have only a few. They tend to appear in phases, with new clusters of blisters appearing in the same area as previous ones.

 

A skin biopsy is usually needed to confirm the diagnosis. For more information, please see our Skin biopsy (punch method) information sheet.

If your child has chronic bullous disease, his or her blood test will show higher levels of antibodies than usual. The skin biopsy will often show IgA antibodies as well which are arranged in a line (“linear” – hence the name that is sometimes used for the condition, linear IgA dermatosis of childhood). Blood tests are often needed to confirm diagnosis.

We are not sure what causes autoimmune disorders such as chronic bullous disease of childhood. More research is needed to discover what triggers antibodies to attack the body instead of fighting foreign invaders like viruses. The condition is not inherited, so cannot be passed on to other children or adults.

Chronic bullous disease of childhood usually appears before the age of five and affects both sexes equally. It also appears to affect all races, but more research is needed to confirm this.

 

 

The aim of treating chronic bullous disease of childhood is to reduce the blistering and associated itching and to prevent any infection. If a blister pops or is scratched so that the surface breaks, this provides a route for infection into the body. If untreated, such an infection may cause serious problems. In the past, before modern medications were developed, this condition and others like it could be fatal if blisters became infected.

A range of treatments are used, including dapsone, ciclosporin and steroids.

Dapsone is a medicine used to treat certain infections but it also has antiinflammatory effects. Steroids like prednisolone are given at a low dose to prevent blisters forming. Ciclosporin suppresses (damps down) the immune system and also prevents blisters forming.

 

The outlook is very good, with no lasting effects. In most children the condition improves suddenly, usually within two years. The blisters do not usually leave any scarring and should not recur

 

 

 

Large, randomized, placebo-controlled, double-blind studies have not been performed for the treatment of linear IgA dermatosis in children or adults. Most cases have been reported to respond to dapsone or sulfapyridine.¹³ Some clinicians favor the use of sulfapyridine because of the lower incidence of adverse effects.¹⁴ However, some patients' conditions may not respond to sulfapyridine but do respond to treatment with dapsone. A response may be seen in 48-72 hours. Other reportedly useful medications include prednisone, sulfamethoxypyridazine, colchicine, dicloxacillin, mycophenolate mofetil, and intravenous immunoglobulin.

Drug-induced disease may be treated merely by withdrawal of the offending agent. In cases of linear IgA dermatosis induced by vancomycin, new lesions stop forming within approximately 2 weeks of withdrawal.¹⁵ Particularly severe cases of drug-induced linear IgA dermatosis respond to a short course of oral corticosteroids

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