The Journal of Dermatology · 2015 · 20 citations · 7 references
MedicineDermatologyPathologyAutoimmunityDermatopathologyImmunopathologyAutoantibodiesAutoimmune Blistering DiseasesAutoimmune DiseasesAutoimmune Skin DiseasesImmunopathology Of SkinInflammatory DermatosesAntibodiesAutoimmune Blistering DermatosesAutoimmune Skin Blistering DisordersAutoimmune Subepidermal Blistering DiseasesBullous DermatosesCutaneous BlisteringHemidesmosomal AntigensSubepidermal Blistering Disorders
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.
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Wolfgang Salmhofer, Yoshie Kawahara, H. Peter Soyer et al. · British Journal of Dermatology · 1997 · 28 citations
Medicine, Dermatology, Pathology +16