Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient
AUTOR(ES)
Antonio, João Roberto, Oliveira, Guilherme Bueno de, Rossi, Natalia Cristina Pires, Pires, Laiza Gabriela Garcia
FONTE
An. Bras. Dermatol.
DATA DE PUBLICAÇÃO
2014-09
RESUMO
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.
Documentos Relacionados
- Autosomal recessive epidermolytic palmoplantar keratoderma.
- Pseudoherpetic keratitis. Corneal changes in circumscribed palmo-plantar keratoderma.
- Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant trait.
- Unique autosomal recessive variant of palmoplantar keratoderma associated with hearing loss not caused by known mutations
- Exuberant pyoderma gangrenosum in a patient with autoimmune hepatitis