Your browser doesn't support javascript.
loading
Erythrokeratodermia Variabilis with Congenital Deaf-Mutism / 대한피부과학회지
Korean Journal of Dermatology ; : 379-381, 2011.
Article in Korean | WPRIM | ID: wpr-100066
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.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Acitretin / Dermis / Deafness / Parturition / Dilatation / Epidermis / Erythema / Erythrokeratodermia Variabilis / Foot Limits: Adult / Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 2011 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Acitretin / Dermis / Deafness / Parturition / Dilatation / Epidermis / Erythema / Erythrokeratodermia Variabilis / Foot Limits: Adult / Female / Humans Language: Korean Journal: Korean Journal of Dermatology Year: 2011 Type: Article