| Literature DB >> 25184927 |
João Roberto Antonio1, Guilherme Bueno de Oliveira1, Natalia Cristina Pires Rossi1, Laiza Gabriela Garcia Pires1.
Abstract
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.Entities:
Mesh:
Year: 2014 PMID: 25184927 PMCID: PMC4155966 DOI: 10.1590/abd1806-4841.20142923
Source DB: PubMed Journal: An Bras Dermatol ISSN: 0365-0596 Impact factor: 1.896