Suppr超能文献

儿童患者的甲下黑素细胞病变。

Subungual Melanocytic Lesions in Pediatric Patients.

机构信息

Servicio de Dermatología, Fundación Instituto Valenciano de Oncología, Valencia, España.

Servicio de Dermatología, Fundación Instituto Valenciano de Oncología, Valencia, España.

出版信息

Actas Dermosifiliogr. 2022 Apr;113(4):388-400. doi: 10.1016/j.ad.2021.10.007. Epub 2021 Nov 11.

Abstract

The study of subungual melanocytic lesions can present challenges because of the clinical and histologic characteristics of the nail unit and the difficulty of performing nail biopsies and processing specimens. These lesions can be even more challenging in children due to differences in clinical and epidemiological profiles between the adult and pediatric populations. Many of the clinical features of subungual melanocytic lesions that would raise alarm in an adult do not have the same implications in children. Consensus is also lacking on when a nail biopsy is needed to rule out malignancy in the pediatric setting. In view of these considerations and the rarity of subungual melanoma in childhood, the recommended approach in most cases is a watch-and-wait strategy. Subungual melanocytic lesions in children may also show atypical histopathologic features that are not necessarily associated with aggressive behavior. Subungual melanoma is very rare in childhood, with just 21 cases described to date. None of the patients developed visceral metastasis or died as a result and the diagnosis was controversial in many of the cases. Considering the above and the significantly higher frequency and particular characteristics of longitudinal melanonychia with a benign etiology in children, subungual melanocytic lesions should be managed differently in this setting than in adults. In most cases, a watch-and-wait approach is the most appropriate strategy.

摘要

甲下黑素细胞病变的研究具有挑战性,这是因为甲单元的临床和组织学特征,以及进行甲活检和处理标本的难度。由于成人和儿童人群的临床和流行病学特征存在差异,这些病变在儿童中更为复杂。许多在成人中引起警觉的甲下黑素细胞病变的临床特征,在儿童中并不具有相同的意义。对于何时需要进行甲活检以排除儿科患者的恶性肿瘤,目前也缺乏共识。鉴于这些考虑因素以及儿童中甲黑色素瘤的罕见性,在大多数情况下,建议采用观察等待策略。儿童的甲下黑素细胞病变也可能表现出非典型的组织病理学特征,这些特征不一定与侵袭性行为相关。儿童期的甲黑色素瘤非常罕见,迄今为止仅描述了 21 例病例。没有患者发生内脏转移或因此而死亡,而且许多病例的诊断存在争议。考虑到上述情况,以及儿童中具有良性病因的纵向黑素甲发病率更高且具有特定特征,在这种情况下,应与成人不同的方式来处理甲下黑素细胞病变。在大多数情况下,观察等待策略是最合适的策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验