Emmert Steffen, Küster Wolfgang, Zutt Markus, Hänssle Holger, Hallermann Christian, Kretschmer Lutz, Neumann Christine
Department of Dermatology, University of Göttingen, von-Siebold-Strasse 3, 37075 Göttingen, Germany.
J Am Acad Dermatol. 2003 Dec;49(6):1166-9. doi: 10.1016/s0190-9622(03)00472-9.
We describe a new family with the rare genodermatosis keratosis punctata palmo-plantaris Buschke-Fischer-Brauer (keratoma disseminatum). In all, 3 family members in 3 generations were affected, a pattern consistent with autosomal dominant inheritance. Clinical symptoms started in the third decade with disseminated, small, round, hyperkeratotic papules on the palms and soles. Punctate keratoses coalesced into hyperkeratotic plaques on pressure points. Identification of additional families is necessary to permit definitive genetic classification of this genodermatosis.
我们描述了一个患有罕见遗传性皮肤病——掌跖点状角化病(Buschke-Fischer-Brauer型,播散性角化瘤)的新家族。三代人中共有3名家族成员患病,这种模式符合常染色体显性遗传。临床症状始于第三个十年,手掌和脚底出现播散性、小而圆的角化过度丘疹。点状角化病在受压部位融合成角化过度斑块。有必要识别更多家族,以便对这种遗传性皮肤病进行明确的基因分类。