Erythrokeratodermia Variabilis with Congenital Deaf-Mutism / 대한피부과학회지
Korean Journal of Dermatology
; : 379-381, 2011.
Article
em Ko
| WPRIM
| ID: wpr-100066
Biblioteca responsável:
WPRO
ABSTRACT
Erythrokeratodermia variabilis is a rare genodermatosis characterized by the coexistence of randomly occurring, transient, erythematous patches and hyperkeratosis of the skin. A 25-year-old Uzbekistanian female with congenital deaf-mutism presented with well demarcated geographic hyperkeratotic patches and bizarre erythema on the whole body surface except the face, hands and feet from birth. The histopathological examination revealed marked hyperkeratosis, moderate acanthosis in the epidermis and vascular dilatation with a perivascular infiltration of inflammatory cells in the upper dermis. Herein we report on a rare case of erythrokeratodermia variabilis with congenital deaf-mutism which was rapidly improved by administering acitretin.
Palavras-chave
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Pele
/
Acitretina
/
Derme
/
Surdez
/
Parto
/
Dilatação
/
Epiderme
/
Eritema
/
Eritroceratodermia Variável
/
Pé
Limite:
Adult
/
Female
/
Humans
Idioma:
Ko
Revista:
Korean Journal of Dermatology
Ano de publicação:
2011
Tipo de documento:
Article