Literature DB >> 22147038

Dowling-Degos disease: classic clinical and histopathological presentation.

Carolina Cotta Zimmermann1, Deborah Sforza, Priscila Marques de Macedo, Luna Azulay-Abulafia, Maria de Fatima G S Alves, Sueli Coelho da S Carneiro.   

Abstract

Dowling-Degos disease (DDD) is a rare genetic disease of the skin (reticulate pigmented anomaly), clinically characterized by flexural brown pigmented reticulate macules, comedo-like papules on the back, neck and pitted perioral or facial scars. We present the case of a 51 year-old man with macrocomedo-like lesions, pitted scars, cysts, hyperpigmented macules in his back, chest, axillae, neck, groin and face. The patient reported having two children, three brothers and a father with a similar condition. The histopathology of the skin biopsies was very characteristic of Dowling-Degos disease, showing dilated follicular, fingerlike projections called rete ridges (dermal pegs), with thinning of the suprapapillary plates, resulting in an "antler-like" pattern and increased pigmentation of the basal layer.

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Year:  2011        PMID: 22147038     DOI: 10.1590/s0365-05962011000500016

Source DB:  PubMed          Journal:  An Bras Dermatol        ISSN: 0365-0596            Impact factor:   1.896


  1 in total

1.  Association of Dowling-Degos disease and multiple seborrheic keratosis in a "Christmas tree pattern".

Authors:  Vitorino Modesto Dos Santos; Nayanne Lays Dos Santos Pereira; Renata Faria Silva; Fabio Henrique de Oliveira Silva; Cacilda Joyce Ferreira da Silva Garcia; Maria Aparecida Alves de Figueiredo Sousa
Journal:  Med J Islam Repub Iran       Date:  2014-07-15
  1 in total

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