Subcorneal pustular dermatosis type of IgA pemphigus: demonstration of autoantibodies to desmocollin-1 and clinical review

Br J Dermatol. 2000 Jul;143(1):144-8. doi: 10.1046/j.1365-2133.2000.03604.x.

Abstract

We describe a 40-year-old Japanese man with a 3-year history of vesiculopustular lesions resembling subcorneal pustular dermatosis. Histopathology showed subcorneal pustules containing a few acantholytic cells, and direct immunofluorescence disclosed IgA deposition in the intercellular space of the upper epidermis. Circulating IgA autoantibodies of very low titre were also demonstrated by indirect immunofluorescence. A novel cDNA transfection technique clearly detected IgA autoantibodies reactive with human desmocollin-1. Combined therapy with dapsone and etretinate improved the skin lesions. We review the clinical features of 49 patients in the literature who presented with vesiculopustular lesions and intraepidermal IgA deposition.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Anti-Infective Agents / therapeutic use
  • Autoantibodies / analysis*
  • Autoantibodies / genetics
  • DNA, Complementary
  • Dapsone / therapeutic use
  • Desmocollins
  • Drug Therapy, Combination
  • Etretinate / therapeutic use
  • Fluorescent Antibody Technique, Direct
  • Humans
  • Immunoglobulin A / analysis*
  • Immunoglobulin A / genetics
  • Keratolytic Agents / therapeutic use
  • Male
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology*
  • Pemphigus / drug therapy
  • Pemphigus / genetics
  • Pemphigus / immunology*
  • Transfection

Substances

  • Anti-Infective Agents
  • Autoantibodies
  • DNA, Complementary
  • DSC1 protein, human
  • Desmocollins
  • Immunoglobulin A
  • Keratolytic Agents
  • Membrane Glycoproteins
  • Etretinate
  • Dapsone