Epidermolytic Hyperkeratosis - case report

Autor: Hayashida,Marcos Takeyoshi, Mitsui,Grasiela Lissa, Reis,Natalia Ivanoff dos, Fantinato,Giovana, Jordão Neto,Domingos, Mercante,Ana Maria da Cunha
Jazyk: angličtina
Rok vydání: 2015
Předmět:
Zdroj: Anais Brasileiros de Dermatologia, Volume: 90, Issue: 6, Pages: 888-891, Published: DEC 2015
Anais Brasileiros de Dermatologia v.90 n.6 2015
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD
Popis: Epidermolytic hipercetarose is a rare genodermatosis, with a prevalence of 1:100.000 to 1:300.000, with autosomal dominant inheritance. We report the case of a 5 year old girlwho presented an hypertrophic verrucous plaques in the neck, under arm, buttocks, knees, pelvis, legs, dorsum of the right foot and elbows. Histological examination of the skin lesions showed typical changes of epidermolytic hyperkeratosis. Because it is an autosomal dominant disorder with complete penetrance, the individual carrying the mutation will necessarily develop the disease. However, in 50% of cases postzygotic mutation occur. The case report emphasizes early diagnosis and differential diagnoses with ichthyosis and other bullous diseases of childhood, as well as discussing the therapeutic possibilities.
Databáze: OpenAIRE