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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...

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Autores principales: Antonio, João Roberto, de Oliveira, Guilherme Bueno, Rossi, Natalia Cristina Pires, Pires, Laiza Gabriela Garcia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2014
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.
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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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