Abstract:
:IgA pemphigus is rare but may be underdiagnosed. We describe two cases, a 50-year-old female with a pustular eruption resembling subcorneal pustular dermatosis and a 55-year-old male with a pruritic vesiculopustular eruption simulating dermatitis herpetiformis. They illustrate the clinical heterogeneity of IgA pemphigus which is likely to reflect differences in autoantigens, analogous to pemphigus vulgaris and pemphigus foliaceus. There is now evidence that IgA pemphigus encompasses at least two subgroups: a subcorneal pustular dermatosis (SPD)-type, (see case 1) characterized by subcorneal pustules and autoantibodies to desmocollin 1; and intra-epidermal neutrophilic dermatosis (IEN)-type cases (see case 2) which show intra-epidermal pustules and in whom the autoantigen may be desmoglein 3, the pemphigus vulgaris antigen.
journal_name
Clin Exp Dermatoljournal_title
Clinical and experimental dermatologyauthors
Harman KE,Holmes G,Bhogal BS,McFadden J,Black MMdoi
10.1046/j.1365-2230.1999.00534.xkeywords:
subject
Has Abstractpub_date
1999-11-01 00:00:00pages
464-6issue
6eissn
0307-6938issn
1365-2230pii
ced534journal_volume
24pub_type
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