Familial porokeratosis Mibelli

Introduction Porokeratoses (PK) are a group of uncommon dermatoses, characterised by a keratinisation disorder, manifesting clinically with annular or linear, well-limited, keratotic plaques and histologically by the presence of the ”cornoid lamella”. Objective To present and discuss a case of the f...

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Published in:Przegląd dermatologiczny 2018-01, Vol.105 (5), p.619-624
Main Authors: Tomaszewska, Katarzyna A., Dominiak, Małgorzata, Zalewska-Janowska, Anna M., Kaszuba, Andrzej
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Language:English
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Dermatology
genetic
Histopathology
Mibelli
porokeratosis
Skin diseases
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container_title Przegląd dermatologiczny
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creator Tomaszewska, Katarzyna A.
Dominiak, Małgorzata
Zalewska-Janowska, Anna M.
Kaszuba, Andrzej
description Introduction Porokeratoses (PK) are a group of uncommon dermatoses, characterised by a keratinisation disorder, manifesting clinically with annular or linear, well-limited, keratotic plaques and histologically by the presence of the ”cornoid lamella”. Objective To present and discuss a case of the familiar porokeratosis Mibelli in 11-year-old girl and her 40-year-old mother. Case report We present the case of an 11-year-old girl and her 40-year-old mother with clearly demarcated, slightly atrophic annular lesions surrounded by slightly scaly hyperkeratotic ridge. In the girl, the lesions were located on the right lower limb, in the mother on both of the shins. The diagnosis was confirmed by histopathological examination. The patients were treated with topical 0.1% adapalene cream. Conclusions The presented case is interesting because of the family occurrence of the disease.
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subjects Dermatology
genetic
Histopathology
Mibelli
porokeratosis
Skin diseases
title Familial porokeratosis Mibelli
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