Anais Brasileiros de Dermatologia | |
Epidermolytic Hyperkeratosis - case report | |
Marcos Takeyoshi Hayashida1  Grasiela Lissa Mitsui1  Natalia Ivanoff Dos Reis1  Giovana Fantinato1  Domingos Jordão Neto1  Ana Maria Da Cunha Mercante1  | |
关键词: Acitretin; Hyperkeratosis; epidermolytic; Ichthyosis bullosa of siemens; | |
DOI : 10.1590/abd1806-4841.20153966 | |
来源: SciELO | |
【 摘 要 】
Abstract: 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.
【 授权许可】
CC BY-NC
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【 预 览 】
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