Mucous membrane pemphigoid with IgG autoantibodies to the 120-kDa ectodomain of type XVII collagen (BP180/linear IgA dermatosis antigen) in a patient with idiopathic thrombocytopenic purpura.

نویسندگان

  • Yuka Hirakawa
  • Naoki Oiso
  • Norito Ishii
  • Hiroshi Koga
  • Megumi Tatebayashi
  • Shusuke Uchida
  • Hiromasa Matsuda
  • Takashi Hashimoto
  • Akira Kawada
چکیده

© 2015 The Authors. doi: 10.2340/00015555-1964 Journal Compilation © 2015 Acta Dermato-Venereologica. ISSN 0001-5555 Mucous membrane pemphigoid (MMP) is an autoimmune subepidermal blistering disease involving primarily the mucosae and occasionally the skin (1–3). We report here a case of a Japanese male patient with idiopathic thrombocytopenic purpura (ITP) who later developed MMP with IgG autoantibodies to the 120-kDa soluble ectodomain of type XVII collagen (BP180) (linear IgA dermatosis antigen; LAD-1).

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عنوان ژورنال:
  • Acta dermato-venereologica

دوره 95 4  شماره 

صفحات  -

تاریخ انتشار 2015