Bullous pemphigoid

Bullous pemphigoid

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Caption: Bullous pemphigoid. Close-up of broken blisters on the skin of a 45-year-old male patient with bullous pemphigoid. This autoimmune skin disease is characterised by the presence of immunoglobulin G (IgG) autoantibodies that attack the skin proteins holding skin cells together at the junction between the epidermis and dermis. This attack results in painful, itchy blisters. Treatment involves corticosteroids or immunosuppressants.

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