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POROQUERATOSIS. REPORTE DE TRES CASOS.

Authors :
Valiente Rebull, Celeste
Rodríguez, Lourdes
Martinez Braga, Gabriela
Di Martino Ortiz, Beatriz
Rodriguez Masi, Mirtha
Knopfelmacher, Oilda
de Lezcano, Lourdes Bolla
Source :
Our Dermatology Online / Nasza Dermatologia Online. Apr2014, Vol. 5 Issue 2, p163-168. 6p.
Publication Year :
2014

Abstract

The porokeratosis are a group of disorders of the skin keratinization of acquired or hereditary character. Its clinical expression is a macular or annular plaque, atrophic in the center and with well-defined hyperkeratotic edges and the histological picture is a compact parakeratotic column, called cornoid lamella. The number and distribution of lesions define the different clinical forms of porokeratosis: Mibelli, disseminated superficial actinic porokeratosis (DSAP), linear porokeratosis, palmoplantar porokeratosis and punctate porokeratosis. We report 3 cases and make a brief review of the literature. [ABSTRACT FROM AUTHOR]

Details

Language :
Spanish
ISSN :
20819390
Volume :
5
Issue :
2
Database :
Academic Search Index
Journal :
Our Dermatology Online / Nasza Dermatologia Online
Publication Type :
Academic Journal
Accession number :
95607029
Full Text :
https://doi.org/10.7241/ourd.20142.40