Porokeratosis of Mibelli - literature review and a case report

Author:

Ferreira Flávia Regina1,Santos Leopoldo Duailibe Nogueira2,Tagliarini Fernando Augusto Nogueira Mendes2,Lira Marcia Lanzoni de Alvarenga2

Affiliation:

1. São Paulo Federal University; University of Taubaté, Brazil

2. University of Taubaté, Brazil

Abstract

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.

Publisher

FapUNIFESP (SciELO)

Subject

Dermatology

Reference10 articles.

1. Facial porokeratosis: A series of six patients;Gutierrez EL;Australas J Dermatol,2010

2. Genital porokeratosis: a series of 10 patients and review of the literature;Chen TJ;Br J Dermatol,2006

3. Poroqueratose de mibelli - um caso clínico (Porokeratosis of Mibelli - a clinical case);Laureano A;Revista SPDV,2012

4. Poroqueratose de Mibelli: uma condição que pode evoluir para neoplasia maligna (Porokeratosis of Mibelli: as a keratotic disorder at risk for malignant transformation);Dal Santo Francisco B;RBM Rev Bras Med,2011

5. Simultaneous occurrence of disseminated superficial, linear and hypertrophic verrucous forms of porokeratosis in a child;Mukhopadhyay AK;Indian J Dermatol Venereol Leprol,2004

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