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A case of antiepiligrin cicatricial pemphigoid with nephrotic syndrome.

AbstractWe report a 71-year-old woman with antiepiligrin cicatricial pemphigoid associated with nephrotic syndrome. She presented with a six-month history of pruritic blisters over her trunk and legs. She also had episodes of recurrent painful oral erosions. A skin biopsy showed a subepidermal bulla, and a direct immunofluorescence (DIF) study revealed linear deposition of IgG and C3 at the basement membrane zone (BMZ). Indirect immunofluorescence (IIF) staining of 1 M NaCl-split skin demonstrated circulating IgG autoantibodies reactive with the dermal side. Immunoprecipitation studies of the patient's serum disclosed IgG autoantibodies directed against a set of polypeptides that corresponded to laminin 5 (beta 3 gamma 2). Based upon the long-standing edema of her legs and her hypoproteinemia, she was diagnosed with nephrotic syndrome. To our knowledge, the association of antiepiligrin cicatricial pemphigoid with nephrotic syndrome has not been reported previously.
AuthorsYuri Uchino, Takuro Kanekura, Koichiro Takeda, Hidehiko Shimada, Mistuse Inoue, Takashi Hashimoto, Tamotsu Kanzaki (Affiliation: Department of Dermatology, Kagoshima University Faculty of Medicine, Kagoshima, Japan.)
JournalThe Journal of dermatology (J Dermatol) Vol. 31 Issue 3 Pg. 228-31 (Mar 2004) ISSN: 0385-2407 [Print] Japan
PMID15187343 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Autoantibodies
  • Cell Adhesion Molecules
  • Immunoglobulin G
  • kalinin
  • Prednisone
Topics
  • Aged
  • Autoantibodies (immunology)
  • Biopsy, Needle
  • Cell Adhesion Molecules (immunology)
  • Female
  • Follow-Up Studies
  • Humans
  • Immunoglobulin G (analysis, immunology)
  • Immunohistochemistry
  • Japan
  • Nephrotic Syndrome (complications, diagnosis, drug therapy, immunology)
  • Pemphigoid, Benign Mucous Membrane (complications, drug therapy, immunology, pathology)
  • Prednisone (therapeutic use)
  • Risk Assessment
  • Treatment Outcome

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