Guaraldi Bianca de Mello, Jaime Thaís Jerez, Guaraldi Rafael de Mello, Melo Daniel Fernandes, Nogueira Osvania Maris, Rodrigues Nilton
Naval Hospital Marcílio Dias (Hospital Naval Marcílio Dias - HNMD), Rio de Janeiro (RJ), Brazil.
An Bras Dermatol. 2013 Jan-Feb;88(1):109-12. doi: 10.1590/s0365-05962013000100016.
Progressive symmetrical erythrokeratodermia is a rare autosomal dominant genodermatosis with variable penetrance described by Darier in 1911. It is characterized by erythematous and keratotic plaques, sharply defined and symmetrically distributed along the extremities, buttocks and, more rarely, on the face. We report a case of a 55-year-old patient with lesions on the dorsum of the hands, interphalangeal pads, wrists, groin and back feet. This case demonstrates a rare and late diagnosis, clinical profusion and presence of familiar involvement.
进行性对称性红斑角化病是一种罕见的常染色体显性遗传性皮肤病,具有可变的外显率,由 Darier 于 1911 年描述。其特征为红斑性和角化性斑块,边界清晰,沿四肢、臀部对称分布,面部较少见。我们报告一例 55 岁患者,其手背、指间垫、手腕、腹股沟和后足出现皮损。该病例显示了罕见的晚期诊断、临床丰富表现及家族性受累情况。