Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient
An. bras. dermatol
;
89(5): 819-821, Sep-Oct/2014. graf
Article
in English
| LILACS
| ID: lil-720792
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.
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Keratoderma, Palmoplantar
Limits:
Aged
/
Humans
/
Male
Language:
English
Journal:
An. bras. dermatol
Journal subject:
Dermatology
Year:
2014
Type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
Faculdade de Medicina de São José do Rio Preto/BR
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