Atopic dermatitis (AD) is a chronic inflammatory skin disease with increasi
ng incidence and socio-economical relevance. The diagnosis is made on clini
cal grounds and different diagnostic criteria sets have been established. T
he majority of all AD cases is associated with a sensitization to environme
ntal allergens and increased serum IgE (so-called extrinsic AD), but about
10-30% of all cases suffer from the so-called intrinsic AD, which obviously
lacks any link to the classical atopic diathesis. The genetic background o
f AD has been investigated by target gene approach by different groups with
mostly contradictory results for each of the genes under study. An imbalan
ce in the spectrum of Th1/Th2 responses, a disturbed prostaglandin metaboli
sm, intrinsic defects in keratinocyte function, delayed eosinophil apoptosi
s, IgE-mediated facilitated antigen presentation by epidermal dendritic cel
ls, a two phase model of the inflammatory response and staphylococcal super
antigen effects are among the currently studied pathogenetical aspects of e
xtrinsic AD, which are reviewed in this paper.