Abstract：
:Immunoglobulin A (IgA) pemphigus is a rare autoimmune blistering disease characterized by epidermal acantholysis and neutrophilic infiltrates, as well as intraepidermal IgA deposits. We report an unusual case of IgA pemphigus involving anal/ perianal skin and oral mucosa that demonstrated a successful response to dapsone treatment.
journal_name
Cutisjournal_title
Cutisauthors
Erdag G,Qureshi HS,Greer KE,Patterson JWsubject
Has Abstractpub_date
2007-09-01 00:00:00pages
218-20issue
3eissn
0011-4162issn
2326-6929journal_volume
80pub_type
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