Froes Giselle Carvalho, Pereira Luciana Baptista, Rocha Vanessa Barreto
Sociedade Brasileira de Dermatologia.
An Bras Dermatol. 2009 Jul-Aug;84(4):425-7. doi: 10.1590/s0365-05962009000400017.
Dyschromatosis symetrica hereditaria (reticulate acropigmentation of Dohi) is a rare autosomal dominant disease. It starts as hyperpigmented and hypopigmented macules in reticular pattern on the extremities. We present a case of a 13-year old boy that showed hyper and hypopigmented macules distributed on the dorsal aspects of the extremities, freckle-like pigmented macules on the face and periorbital atrophic linear lesions. Differentiation with others reticulate pigmentation manifestations is necessary.
遗传性对称性色素异常症(土肥网状肢端色素沉着症)是一种罕见的常染色体显性疾病。其起病表现为四肢出现网状分布的色素沉着斑和色素减退斑。我们报告一例13岁男孩病例,其四肢背侧出现色素沉着斑和色素减退斑,面部有雀斑样色素沉着斑,眶周有萎缩性线性损害。有必要与其他网状色素沉着表现相鉴别。