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Mucous membrane pemphigoid
Article en En | WPRIM | ID: wpr-626053
Biblioteca responsable: WPRO
ABSTRACT
Mucous membrane pemphigoid is a group of putative autoimmune, chronic inflammatory, subepithelial blistering diseases predominantly affecting mucous membranes, characterised by linear deposition of IgG, IgA, or C3 along the epithelial basement membrane1. This variant of pemphigoid is rare and encompasses a heterogeneous group manifesting a varying constellation of oral, ocular, skin, genital, nasopharyngeal, oesophageal and laryngeal lesions. In severe cases, it may lead to blindness due to ocular involvement and may even be life threatening due to airway obstruction. We report a case of mucous membrane pemphigoid with oral and genital involvement.
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Texto completo: 1 Índice: WPRIM Idioma: En Revista: Malaysian Journal of Dermatology Año: 2009 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Idioma: En Revista: Malaysian Journal of Dermatology Año: 2009 Tipo del documento: Article