Goettmann-Bonvallot S, André J, Belaich S
Department of Dermatology, Hôpital Bichat, Paris, France.
J Am Acad Dermatol. 1999 Jul;41(1):17-22. doi: 10.1016/s0190-9622(99)70399-3.
Very little has been published on longitudinal melanonychia in children. Our objective was to determine the nature of melanocytic lesions in pediatric patients with longitudinal or total melanonychia and to look for correlations between clinical and histologic features.
All patients younger than 16 years of age with longitudinal or total melanonychia who were evaluated at our nail disorder outpatient clinic between September 1993 and September 1996 were included. The clinical and histologic features of the nail condition were determined in each case.
Forty patients were included. The final diagnosis was nevus in 19 cases (junctional in 17 cases and compound in 2), lentigo in 12 cases, and functional longitudinal melanonychia in 9. The latter corresponded to a hyperpigmentation caused by melanocytic activation with no increase in the number of melanocytes. None of the patients had melanoma. Appearance within the first year of life, periungual pigmentation, and total melanonychia were consistent features in patients with melanocytic hyperplasia (lentigo or nevus). Early onset of a dark broad lesion in a white patient was typical of melanocytic hyperplasia, although none of these features were pathognomonic.
Benign melanocytic hyperplasia (lentigo or nevus) was the cause of 77.5% of cases of longitudinal melanonychia in our overall pediatric population and of 85% of cases in the subset of white patients. All the remaining cases of longitudinal melanonychia were the result of melanocytic activation.
关于儿童纵向黑甲的研究报道极少。我们的目的是确定患有纵向或全甲黑甲的儿科患者黑素细胞病变的性质,并寻找临床和组织学特征之间的相关性。
纳入1993年9月至1996年9月期间在我们的甲病门诊接受评估的所有16岁以下患有纵向或全甲黑甲的患者。确定每例患者甲病的临床和组织学特征。
共纳入40例患者。最终诊断为痣19例(交界痣17例,复合痣2例),雀斑样痣12例,功能性纵向黑甲9例。后者对应于黑素细胞活化引起的色素沉着,黑素细胞数量无增加。所有患者均未患黑色素瘤。黑素细胞增生(雀斑样痣或痣)患者的一致特征为出生后第一年内出现、甲周色素沉着和全甲黑甲。白人患者中早期出现深色宽大病变是黑素细胞增生的典型表现,尽管这些特征均无诊断特异性。
在我们的总体儿科人群中,良性黑素细胞增生(雀斑样痣或痣)是77.5%的纵向黑甲病例的病因,在白人患者亚组中是85%的病例的病因。所有其余的纵向黑甲病例均为黑素细胞活化的结果。