| Literature DB >> 25708520 |
Akiko Imanishi1, Chiharu Tateishi, Hisayoshi Imanishi, Junko Sowa-Osako, Hiroshi Koga, Daisuke Tsuruta, Takashi Hashimoto.
Abstract
Both anti-laminin γ1 pemphigoid and bullous pemphigoid are autoimmune subepidermal blistering diseases. The former is rare and characterized by autoantibodies to laminin γ1, a 200-kDa dermal protein, while the latter is common among the elderly and characterized by autoantibodies to BP180 and BP230, both of which are hemidesmosomal proteins. We experienced a 69-year-old Japanese male patient with blister formation secondary to erythrodermic psoriasis, which was successfully treated with cyclosporin. The histopathology of erythema corresponded with psoriasis and that of a blistering lesion showed infiltration of neutrophils and eosinophils in and around the subepidermal blisters. Patient immunoglobulin G antibodies labeled both the epidermal and dermal sides of 1 mol/L NaCl-split human skin by indirect immunofluorescent microscopy and recognized laminin γ1, BP180 and BP230 by immunoblotting. To the best of our knowledge, this is the first report of coexistence of psoriasis and atypical pemphigoid with these three autoantibodies.Entities:
Keywords: BP180; cyclosporin; laminin γ1; pemphigoid; psoriasis
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Year: 2015 PMID: 25708520 DOI: 10.1111/1346-8138.12798
Source DB: PubMed Journal: J Dermatol ISSN: 0385-2407 Impact factor: 4.005