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首页> 外文期刊>Case Reports in Dermatological Medicine >Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s Lines
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Asymmetric Bilateral Lichen Striatus: A Rare Presentation following Multiple Blaschko’s Lines

机译:不对称的双侧地衣纹状体:多条Blaschko线后的稀有表现

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Lichen striatus (LS) is an uncommon, acquired, self-limited, and benign linear dermatosis of unknown etiology that most often occurs unilaterally and is confined to the lines of Blaschko. A healthy 7-year-old girl presented to our clinic with bilateral asymmetric LS occurring on the right arm and left leg of 1-year duration. Very few cases of bilateral LS have been previously reported in the literature, with none from clinics within the United States. The etiology of LS is currently unknown; however its confinement to Blaschko’s lines, which represent embryologic migration of skin cell clones, does provide insight into a possible pathogenesis. It seems most likely that an individual’s development of LS is linked to their genetic predisposition and a subsequent triggering event. Our case serves as a strong example of a rare presentation of LS and facilitates discussion of the clinical diagnostic process and possible pathogenesis of this dermatosis.
机译:地衣纹状体(LS)是一种病因不明的罕见,获得性,自限性和良性线性皮肤病,通常单方面发生,并局限于Blaschko系。一名健康的7岁女孩就诊于我们的诊所,病程为1年,右臂和左腿出现双侧不对称LS。先前文献中报道的双侧LS病例很少,美国的诊所也没有。 LS的病因目前未知。但是,将其限制在代表皮肤细胞克隆的胚胎迁移的Blaschko品系中,确实可以洞悉可能的发病机理。个体的LS发育很可能与他们的遗传易感性和随后的触发事件有关。我们的病例是罕见的LS表现的有力例证,并促进了这种皮肤病的临床诊断过程和可能的发病机理的讨论。

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