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Granuloma faciale: a rare disease from a dermoscopy perspective

The granuloma faciale is a rare and benign skin disease of unknown etiology, characterized by chronic leukocitoclastic vasculitis. It is characterized by skin lesions predominantly facial whose course is chronic and slowly progressive. The diagnosis is based on clinical features, histopathology and,...

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Autores principales: Teixeira, Danilo Augusto, Estrozi, Bruna, Ianhez, Mayra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875968/
https://www.ncbi.nlm.nih.gov/pubmed/24346891
http://dx.doi.org/10.1590/abd1806-4841.20132384
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author Teixeira, Danilo Augusto
Estrozi, Bruna
Ianhez, Mayra
author_facet Teixeira, Danilo Augusto
Estrozi, Bruna
Ianhez, Mayra
author_sort Teixeira, Danilo Augusto
collection PubMed
description The granuloma faciale is a rare and benign skin disease of unknown etiology, characterized by chronic leukocitoclastic vasculitis. It is characterized by skin lesions predominantly facial whose course is chronic and slowly progressive. The diagnosis is based on clinical features, histopathology and, more recently, in dermoscopy. We describe the case of a male patient, 40 years old, with a sarcoid lesion on the malar site, whose histopathological examination revealed a mixed inflammatory infiltrate with presence of Grenz zone. Dermoscopy revealed a pink background with white striations. The definitive diagnosis is made by histopathologic evaluation, and dermatoscopy can be helpful. It is known to be resistant to therapy, oral medications, intralesional and surgical procedures are options.
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spelling pubmed-38759682014-01-08 Granuloma faciale: a rare disease from a dermoscopy perspective Teixeira, Danilo Augusto Estrozi, Bruna Ianhez, Mayra An Bras Dermatol Case Report The granuloma faciale is a rare and benign skin disease of unknown etiology, characterized by chronic leukocitoclastic vasculitis. It is characterized by skin lesions predominantly facial whose course is chronic and slowly progressive. The diagnosis is based on clinical features, histopathology and, more recently, in dermoscopy. We describe the case of a male patient, 40 years old, with a sarcoid lesion on the malar site, whose histopathological examination revealed a mixed inflammatory infiltrate with presence of Grenz zone. Dermoscopy revealed a pink background with white striations. The definitive diagnosis is made by histopathologic evaluation, and dermatoscopy can be helpful. It is known to be resistant to therapy, oral medications, intralesional and surgical procedures are options. Sociedade Brasileira de Dermatologia 2013 /pmc/articles/PMC3875968/ /pubmed/24346891 http://dx.doi.org/10.1590/abd1806-4841.20132384 Text en ©2013 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Teixeira, Danilo Augusto
Estrozi, Bruna
Ianhez, Mayra
Granuloma faciale: a rare disease from a dermoscopy perspective
title Granuloma faciale: a rare disease from a dermoscopy perspective
title_full Granuloma faciale: a rare disease from a dermoscopy perspective
title_fullStr Granuloma faciale: a rare disease from a dermoscopy perspective
title_full_unstemmed Granuloma faciale: a rare disease from a dermoscopy perspective
title_short Granuloma faciale: a rare disease from a dermoscopy perspective
title_sort granuloma faciale: a rare disease from a dermoscopy perspective
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875968/
https://www.ncbi.nlm.nih.gov/pubmed/24346891
http://dx.doi.org/10.1590/abd1806-4841.20132384
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