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The bullae are formed by an immune reaction, initiated by the formation of IgG [citation needed] autoantibodies targeting dystonin, also called bullous pemphigoid antigen 1, [6] and/or type XVII collagen, also called bullous pemphigoid antigen 2, [7] which is a component of hemidesmosomes. A different form of dystonin is associated with ...
Bullous pemphigoid. Bullous pemphigoid is an autoimmune bullous disease that mainly affects older individuals. Individuals typically present with itchy rashes that transform into fluid filled bullous lesions on the skin. Although these blisters usually appear on the arms, legs, and trunk of the body, they can also be found in the mouth as sores.
Bullous pemphigoid is primarily a disease of older adults and it rarely occurs in children. The vast majority of cases involved individuals between the ages of 60 and 80 years. Two European studies have also suggested the increased risk of bullous pemphigoid with advancing age.
Bullous pemphigoid: Skin Anti-BP180, Anti-BP230 Confirmed 6-30 per 100,000 (mostly older adults) [7] Cicatricial pemphigoid: Mucous membranes, sometimes skin Anti-BP180, Anti-BP230 Confirmed Rare [8] Dermatitis herpetiformis: Skin Anti-tissue transglutaminase: Confirmed 10 per 100,000 [9] Dermatomyositis: Skin and muscles: Anti-Jo1, Anti-Mi2 ...
Adult linear IgA disease is an acquired, autoimmune blistering disease that may present with a clinical pattern of vesicles indistinguishable from dermatitis herpetiformis, or with vesicles and bullae in a bullous pemphigoid-like appearance. [2] This disease can often be difficult to treat even with usually effective medications such as ...
Antibody isotype(s) and location of antibody deposition in immunofluorescence studies using salt-split skin for autoimmune bullous conditions targeting the basement membrane zone of the human integumentary system Condition Antibody isotype(s) deposited Localization of antibody with use of salt-split skin Antiepilegrin cicatricial pemphigoid ...
Paraneoplastic pemphigus (PNP) is an autoimmune disorder stemming from an underlying tumor.It is hypothesized that antigens associated with the tumor trigger an immune response resulting in blistering of the skin and mucous membranes.
Overall prognosis is good in most patients, with one study showing recovery occurring in 94% and 89% of children and adults, respectively (some having needed treatment). [27] In children under ten, the condition recurs in about a third of all cases, usually within the four months of the initial attack. [ 6 ]