Swerdlow A J, Green A
Office of Population Censuses and Surveys, London, U.K.
Br J Dermatol. 1987 Aug;117(2):137-46. doi: 10.1111/j.1365-2133.1987.tb04109.x.
There is growing evidence that individuals at high risk of cutaneous melanoma can be identified by the use of simple measures of benign melanocytic naevi--raised risk occurring in persons who have large numbers of naevi, or naevi with atypical clinical features. Very high risk of melanoma appears to exist in two rare groups: persons with dysplastic naevi whose families include at least two individuals who have had melanoma, and persons with giant congenital naevi. Risks of melanoma in other individuals with dysplastic naevi and in persons with small congenital naevi have not yet been quantified. Much of the published work on risk of melanoma in relation to naevi has been based on clinical series or assemblage of case reports, with great potential for bias. In such studies, naevi have often been classified into dichotomies or syndromes originally defined for pathological or clinical purposes, frequently using poorly reproducible criteria. Case-control and cohort studies of the relationship of naevi to melanoma are needed, which use reproducible criteria and designs minimizing bias, and which examine risk in relation to graded clinical and histological measures of naevi.
越来越多的证据表明,通过使用简单的良性黑素细胞痣测量方法,可以识别出皮肤黑色素瘤的高危个体——痣数量多或具有非典型临床特征的人患癌风险增加。黑色素瘤的极高风险似乎存在于两个罕见群体中:发育异常痣患者,其家族中至少有两名患过黑色素瘤的个体;以及巨大先天性痣患者。其他发育异常痣个体和小先天性痣患者的黑色素瘤风险尚未量化。许多已发表的关于痣与黑色素瘤风险关系的研究都基于临床系列或病例报告的汇总,存在很大的偏倚可能性。在这类研究中,痣常常被分为最初为病理或临床目的定义的二分法或综合征,经常使用难以重复的标准。需要进行痣与黑色素瘤关系的病例对照和队列研究,这些研究应使用可重复的标准和设计,尽量减少偏倚,并根据痣的分级临床和组织学测量来检查风险。