Suppr超能文献

先天性巨痣:治疗管理和黑色素瘤风险:系统评价。

Large congenital melanocytic nevi: therapeutic management and melanoma risk: a systematic review.

机构信息

Dermatology Department, Centre Hospitalier Universitaire de Nantes, Nantes, France.

出版信息

J Am Acad Dermatol. 2013 Mar;68(3):493-8.e1-14. doi: 10.1016/j.jaad.2012.09.039. Epub 2012 Nov 19.

Abstract

BACKGROUND

Large congenital melanocytic nevi (LCMN) are defined as congenital melanocytic nevi having a projected adult size exceeding 20 cm in diameter. They occur in 1 in 20,000 to 1 in 500,000 newborns. Therapeutic management of LCMN remains controversial and is often decided according to melanoma risk.

OBJECTIVE

We sought to synthesize all data available on LCMN-associated melanoma risk, therapeutic assessment, and psychosocial and aesthetic impacts.

METHODS

A MEDLINE search was conducted (1966-February 2011), and 22 French- and English-language databases were consulted. Case reports and reviews were excluded, as were studies with fewer than 20 patients and insufficient information about the nevi. Studies were qualitatively assessed and analyzed according to predefined criteria.

RESULTS

Fourteen studies were selected (956 references). A total of 52 (2%) melanomas (2 in 1 patient) developed in 2578 patients. Age at diagnosis ranged from birth to 58 (mean 12.6) years. Primary melanomas were mostly cutaneous (82%) and 68% were located on the trunk; 7 melanomas were visceral. Melanoma-associated LCMN size exceeded 40 cm for 74% and 94% had satellite nevi. Of melanomas, 55% were fatal, with age at death ranging from 0.9 to 40 (mean 10) years. Eighteen patients were still alive with a mean follow-up of 10.2 years. Melanoma incidence assessable for 216 cases was estimated at 2.3 per 1000 patient-years. Behavioral/emotional problems independent of the lesion were common in children.

LIMITATIONS

Selected studies were heterogeneous.

CONCLUSION

LCMN management should be individualized with respect to melanoma risk, and aesthetic and psychosocial aspects.

摘要

背景

先天性巨大黑素细胞痣(LCMN)被定义为预测成人大小超过 20cm 直径的先天性黑素细胞痣。它们在每 2 万至 5 万新生儿中发生 1 例。LCMN 的治疗管理仍然存在争议,通常根据黑色素瘤的风险来决定。

目的

我们旨在综合所有关于 LCMN 相关黑色素瘤风险、治疗评估以及心理社会和美学影响的可用数据。

方法

我们进行了 MEDLINE 检索(1966 年至 2011 年 2 月),并查阅了 22 种法语和英语数据库。排除了病例报告和综述,以及患者少于 20 例和痣信息不足的研究。根据预先确定的标准对研究进行定性评估和分析。

结果

选择了 14 项研究(956 篇参考文献)。在 2578 例患者中共有 52 例(2%)黑色素瘤(1 例中有 2 例)发生。诊断时的年龄范围从出生到 58 岁(平均 12.6 岁)。原发性黑色素瘤主要位于皮肤(82%),68%位于躯干;7 例黑色素瘤为内脏。与黑色素瘤相关的 LCMN 大小超过 40cm 的占 74%,94%有卫星痣。黑色素瘤中,55%是致命的,死亡年龄从 0.9 岁到 40 岁(平均 10 岁)。18 例患者仍存活,平均随访 10.2 年。可评估的 216 例黑色素瘤的发病率估计为每 1000 例患者年 2.3 例。与病变无关的行为/情绪问题在儿童中很常见。

局限性

所选研究存在异质性。

结论

LCMN 的管理应根据黑色素瘤的风险、美学和心理社会方面进行个体化。

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