Coutinho Inês, Gameiro Ana Rita, Gouveia Miguel Pinto, Cardoso José Carlos, Figueiredo Américo
Centro Hospitalar Universitário de Coimbra, Coimbra, PT.
An Bras Dermatol. 2015 May-Jun;90(3 Suppl 1):153-5. doi: 10.1590/abd1806-4841.20153440.
Multiple minute digitate hyperkeratosis is a rare, non-follicular dermatosis, with fewer than 30 cases described worldwide. It can be either acquired or inherited in an autosomal dominant pattern. We describe the case of an 83-year old patient with life-long, multiple, digitate, milimetric lesions, and a positive family history for the same dermatosis.
多发性微小指状角化过度症是一种罕见的非毛囊性皮肤病，全球报道的病例少于30例。它可以是获得性的，也可以以常染色体显性模式遗传。我们描述了一位83岁患者的病例，该患者有终生多发性指状毫米大小的皮损，且有相同皮肤病的家族史阳性。
