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Papular elastorrhexis: a rare and benign disease
Papular elastorrhexis is an acquired disease of elastic tissue; considered rare, its etiology and pathogenesis remain unknown. The vast majority of cases occur in women in the first or second decade of life. The disease manifests as multiple uniformly-sized, circumscribed, hypochromic and achromic p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063121/ https://www.ncbi.nlm.nih.gov/pubmed/30066768 http://dx.doi.org/10.1590/abd1806-4841.20187317 |
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author | de Bem, Layla Comel Corso Perito Coppini, Alessandra Padilha, Vanessa Vinderfeltes de Lima, Brunno Zeni |
author_facet | de Bem, Layla Comel Corso Perito Coppini, Alessandra Padilha, Vanessa Vinderfeltes de Lima, Brunno Zeni |
author_sort | de Bem, Layla Comel Corso Perito |
collection | PubMed |
description | Papular elastorrhexis is an acquired disease of elastic tissue; considered rare, its etiology and pathogenesis remain unknown. The vast majority of cases occur in women in the first or second decade of life. The disease manifests as multiple uniformly-sized, circumscribed, hypochromic and achromic papules located predominantly on the trunk and upper extremities. The lesions are generally asymptomatic and have a stable evolution over years. Its diagnosis is based on clinical and histopathological findings. The benignity of papular elastorrhexis and the subtlety of its clinical changes make the expectant treatment perfectly viable. The authors present one case in a young female patient. |
format | Online Article Text |
id | pubmed-6063121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-60631212018-08-07 Papular elastorrhexis: a rare and benign disease de Bem, Layla Comel Corso Perito Coppini, Alessandra Padilha, Vanessa Vinderfeltes de Lima, Brunno Zeni An Bras Dermatol Case Report Papular elastorrhexis is an acquired disease of elastic tissue; considered rare, its etiology and pathogenesis remain unknown. The vast majority of cases occur in women in the first or second decade of life. The disease manifests as multiple uniformly-sized, circumscribed, hypochromic and achromic papules located predominantly on the trunk and upper extremities. The lesions are generally asymptomatic and have a stable evolution over years. Its diagnosis is based on clinical and histopathological findings. The benignity of papular elastorrhexis and the subtlety of its clinical changes make the expectant treatment perfectly viable. The authors present one case in a young female patient. Sociedade Brasileira de Dermatologia 2018 /pmc/articles/PMC6063121/ /pubmed/30066768 http://dx.doi.org/10.1590/abd1806-4841.20187317 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivative License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited and the work is not changed in any way. |
spellingShingle | Case Report de Bem, Layla Comel Corso Perito Coppini, Alessandra Padilha, Vanessa Vinderfeltes de Lima, Brunno Zeni Papular elastorrhexis: a rare and benign disease |
title | Papular elastorrhexis: a rare and benign disease |
title_full | Papular elastorrhexis: a rare and benign disease |
title_fullStr | Papular elastorrhexis: a rare and benign disease |
title_full_unstemmed | Papular elastorrhexis: a rare and benign disease |
title_short | Papular elastorrhexis: a rare and benign disease |
title_sort | papular elastorrhexis: a rare and benign disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063121/ https://www.ncbi.nlm.nih.gov/pubmed/30066768 http://dx.doi.org/10.1590/abd1806-4841.20187317 |
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