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首页> 外文期刊>Pediatric dermatology >Linear and whorled hypermelanosis.
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Linear and whorled hypermelanosis.

机译:线性和轮状黑色素过多症。

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Linear and whorled nevoid hypermelanosis is a sporadic pigmentary anomaly occurring within the first weeks of life, characterized clinically by swirls and streaks of macular hyperpigmentation following the lines of Blaschko. Histologically it shows only epidermal melanosis. Underlying chromosomal mosaicism has been demonstrated in only a few published cases. Progressive cribriform and zosteriform hyperpigmentation is considered to be the localized variant of linear and whorled nevoid hypermelanosis. We report a retrospective study on 16 children referred consecutively over a 10-year period for evaluation of segmental, linear or swirled hyperpigmentation distributed along the lines of Blashko, consistent with a diagnosis of linear and whorled nevoid hypermelanosis. Associated abnormalities were found only in one out of six patients with the diffuse form (linear and whorled nevoid hypermelanosis-type) and in none of the remaining 10 children presenting the unilateral form (progressive cribriform and zosteriform hyperpigmentation-type). A long-term follow-up did not disclose further abnormalities. The authors discuss the nosologic position of this entity with respect to hypomelanosis of Ito. Linear and whorled nevoid hypermelanosis and hypomelanosis of Ito should be not considered single entities, but be rather grouped as a heterogeneous collection of nonspecific pigmentary disorders caused by genetic mosaicism. Skin findings in these diseases can differ according to the pigmentation in the normal cell line and whether the second line contains more or less melanosomes than the normal skin of the individual exhibiting mosaicism.
机译:线状和轮状无间隙黑色素增生是在生命的最初几周内发生的偶发性色素异常,其临床特征是遵循Blaschko线的黄斑色素沉着的漩涡和条纹。从组织学上讲,它仅显示表皮黑素病。仅在少数已发表的病例中证明了潜在的染色体镶嵌。渐进性筛状和带状状色素沉着被认为是线性和轮生的避免性黑色素过多症的局部变异。我们报告了一项回顾性研究,该研究在10年期间连续被转介以评估沿Blashko线分布的节段性,线性或漩涡状色素沉着的儿童,与诊断为线性和螺旋状的避免黑色素过多症有关。仅在六分之一的弥散型患者中发现了相关异常(线性和轮状的无黑色素过多型),而其余的十名单侧患者(渐进性网状和带状色素沉着型)中均未发现相关异常。长期随访未发现更多异常情况。作者讨论了该实体在伊藤黑素瘤病方面的疾病学地位。 Ito的线性和螺旋状避免黑色素过多和黑色素不足不应被视为单个实体,而应归类为由遗传镶嵌引起的非特异性色素异常的异质性集合。根据正常细胞系中的色素沉着以及第二系是否包含比显示出花叶病的个体的正常皮肤更多或更少的黑素体,这些疾病的皮肤发现可能会有所不同。

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