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Porokeratosis of Mibelli - literature review and a case report

Porokeratosis is a disorder of epidermal keratinization characterized by annular plaques with an atrophic center and hyperkeratotic edges, and includes a heterogeneous group of disorders that are mostly inherited in an autosomal dominant form. This report describes a 5 year-old female patient, with...

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Detalles Bibliográficos
Autores principales: Ferreira, Flávia Regina, Santos, Leopoldo Duailibe Nogueira, Tagliarini, Fernando Augusto Nogueira Mendes, Lira, Marcia Lanzoni de Alvarenga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876017/
https://www.ncbi.nlm.nih.gov/pubmed/24346913
http://dx.doi.org/10.1590/abd1806-4841.20132721
Descripción
Sumario:Porokeratosis is a disorder of epidermal keratinization characterized by annular plaques with an atrophic center and hyperkeratotic edges, and includes a heterogeneous group of disorders that are mostly inherited in an autosomal dominant form. This report describes a 5 year-old female patient, with porokeratosis of Mibelli confirmed histopathologically. The rarity of this disorder, its clinical exuberance and the destructive character of the lesions, as well as the facial and mucosal involvements, unusual in this form of porokeratosis, and also its onset in early childhood motivated this report.