Title of article
Lichen planus pemphigoides: A case report
Author/Authors
Farshchian, Mahmood Department of Dermatology - Hamadan University of Medical Sciences, Hamadan , Rahmatpour, Ghasem Department of Dermatology - Hamadan University of Medical Sciences, Hamadan
Pages
3
From page
32
To page
34
Abstract
Lichen planus pemphigoides (LPP) is a rare autoimmune blistering disease that is characterized by the development of vesico-bullous skin lesions in patients with lichen planus. The histopathology of LPP reveals a sub_epidermal blister with linear deposition of IgG and /or C3 along the dermal_epidermal junction (DEJ) upon direct immunofluorescence (DIF). We hereunder describe
a case of lichen planus pemphigoides in a 69-year-old otherwise healthy male who initially presented with typical lesions of lichen planus (LP), predominantly on the lower extremities; then, bullous lesions developed on the normal skin.
Keywords
bullous pemphigoid , lichen planus pemphigoides , lichen planus , bullous disease , direct immunofluorescence
Journal title
Astroparticle Physics
Serial Year
2011
Record number
2479864
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