Case Reports in Dermatology · 2013 · 23 citations · 4 references
MedicineDermatologyPathologyAutoimmunityDermatopathologyHistopathologyAutoantibodiesAutoimmune Skin DiseasesDrug-induced Skin ReactionsImmunopathology Of SkinPruritic Skin DiseaseBasement Membrane Zone AntigensBullous DermatosesBullous Lichen PlanusCutaneous Lichen PlanusImmunofluorescence FindingsImmunofluorescence StainingIndirect Immunofluorescence AssayPrednisolone Use
Lichen planus pemphigoides (LPP) is a rare clinical variant of bullous pemphigoid (BP). A 35-year-old female patient presented to our hospital complaining of pruritic violaceous-colored plaques or papules on the extremities. Tense vesicles were also seen on the soles. Skin biopsies from the papules and vesicles demonstrated lichen planus and BP, respectively. Direct immunofluorescence demonstrated linear IgG and C3 deposition on the basement membrane zone. Indirect immunofluorescence on 1 M NaCl split skin detected IgG reactivity with the epidermal side. Enzyme-linked immunosorbent assay also detected anti-BP180 antibodies. After treatment with oral prednisolone alone had failed, low-dose cyclosporine A (CyA) was added. The clinical symptoms immediately improved and the titer of the anti-BP180 antibodies decreased. Although there is little information about the treatment of recalcitrant LPP, additional CyA appeared to be beneficial.
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Coexistence of lichen planus and bullous pemphigoid.
G Stingl, Karl Holubar · British Journal of Dermatology · 1975 · 121 citations
Medicine, Dermatology, Pathology +10