Anais Brasileiros de Dermatologia (Sep 2014)

Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient

  • João Roberto Antonio,
  • Guilherme Bueno de Oliveira,
  • Natalia Cristina Pires Rossi,
  • Laiza Gabriela Garcia Pires

DOI
https://doi.org/10.1590/abd1806-4841.20142923
Journal volume & issue
Vol. 89, no. 5
pp. 819 – 821

Abstract

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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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