Dermatitis herpetiformis

A chronic autoimmune subepidermal bullous disease characterized by grouped pruritic lesions such as papules, urticarial plaques, erythema, and herpetiform vesiculae, with a predominantly symmetrical distribution on extensor surfaces of the elbows (90%), knees (30%), shoulders, buttocks, sacral region, and face of children and adults. Erosions, excoriations and hyperpigmentation usually follow. It may also appear as a consequence of gluten intolerance.

Partial IgA deficiency

Detectable but decreased IgA levels that are more than 2 standard deviations below normal age-adjusted means.


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PMID (PMCID)
16631941
MALE Adult
Dermatitis herpetiformis and partial IgA deficiency.
Samolitis NJ, Hull CM, Leiferman KM, Zone JJ.
J Am Acad Dermatol. 2006;54(5 Suppl):S206-9.
Dermatitis herpetiformis and partial IgA deficiency.