Facial porokeratosis: A series of six patients

Ericson L. Gutierrez, Carlos Galarza, Willy Ramos, Mercedes Tello, Patricia Chávez De Paz, Lucia Bobbio, Alicia Barquinero, Gerardo Ronceros, Alex G. Ortega-Loayza

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Abstract

Porokeratosis is a disorder of epidermal keratinization characterized by annular plaques with an atrophic centre and hyperkeratotic edges, and includes a heterogeneous group of disorders that are mostly inherited in an autosomal dominant fashion. Facial porokeratosis is rare and is not well documented. We present six cases of facial porokeratosis seen over a period of 15 years in a hospital in Lima, Peru. In most of the cases, porokeratosis was found in younger women without any significant past medical history. Oral isotretinoin showed moderate improvement in two of our patients. © 2010 The Australasian College of Dermatologists.
Original languageAmerican English
Pages (from-to)191-194
Number of pages4
JournalAustralasian Journal of Dermatology
DOIs
StatePublished - 1 Aug 2010

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    Gutierrez, E. L., Galarza, C., Ramos, W., Tello, M., De Paz, P. C., Bobbio, L., Barquinero, A., Ronceros, G., & Ortega-Loayza, A. G. (2010). Facial porokeratosis: A series of six patients. Australasian Journal of Dermatology, 191-194. https://doi.org/10.1111/j.1440-0960.2009.00616.x