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Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient
Buschke-Fisher-Brauer keratoderma is a rare hereditary autosomal dominant disease of incomplete penetrance. Important differential diagnoses include other palmoplantar keratinization disorders, acquired or hereditary, which is done based on the histopathological findings. This diagnosis alerts espec...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155966/ https://www.ncbi.nlm.nih.gov/pubmed/25184927 http://dx.doi.org/10.1590/abd1806-4841.20142923 |
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author | Antonio, João Roberto de Oliveira, Guilherme Bueno Rossi, Natalia Cristina Pires Pires, Laiza Gabriela Garcia |
author_facet | Antonio, João Roberto de Oliveira, Guilherme Bueno Rossi, Natalia Cristina Pires Pires, Laiza Gabriela Garcia |
author_sort | Antonio, João Roberto |
collection | PubMed |
description | Buschke-Fisher-Brauer keratoderma is a rare hereditary autosomal dominant disease of incomplete penetrance. Important differential diagnoses include other palmoplantar keratinization disorders, acquired or hereditary, which is done based on the histopathological findings. This diagnosis alerts especially about the possibility of associated neoplasms. Treatment involves topical keratolytic agents, usually with little efficacy, or with long-term systemic retinoids with follow-up of exuberant collateral effects. |
format | Online Article Text |
id | pubmed-4155966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-41559662014-09-09 Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient Antonio, João Roberto de Oliveira, Guilherme Bueno Rossi, Natalia Cristina Pires Pires, Laiza Gabriela Garcia An Bras Dermatol Case Report Buschke-Fisher-Brauer keratoderma is a rare hereditary autosomal dominant disease of incomplete penetrance. Important differential diagnoses include other palmoplantar keratinization disorders, acquired or hereditary, which is done based on the histopathological findings. This diagnosis alerts especially about the possibility of associated neoplasms. Treatment involves topical keratolytic agents, usually with little efficacy, or with long-term systemic retinoids with follow-up of exuberant collateral effects. Sociedade Brasileira de Dermatologia 2014 /pmc/articles/PMC4155966/ /pubmed/25184927 http://dx.doi.org/10.1590/abd1806-4841.20142923 Text en ©2014 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 Antonio, João Roberto de Oliveira, Guilherme Bueno Rossi, Natalia Cristina Pires Pires, Laiza Gabriela Garcia Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient |
title | Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar
keratoderma in bedridden patient
|
title_full | Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar
keratoderma in bedridden patient
|
title_fullStr | Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar
keratoderma in bedridden patient
|
title_full_unstemmed | Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar
keratoderma in bedridden patient
|
title_short | Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar
keratoderma in bedridden patient
|
title_sort | exuberant clinical picture of buschke-fischer-brauer palmoplantar
keratoderma in bedridden patient |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155966/ https://www.ncbi.nlm.nih.gov/pubmed/25184927 http://dx.doi.org/10.1590/abd1806-4841.20142923 |
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