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黑人先天性黑素细胞痣的恶变风险。

Risk of malignant transformation of congenital melanocytic nevi in blacks.

作者信息

Shpall S, Frieden I, Chesney M, Newman T

机构信息

Department of Dermatology, University of California, San Francisco 94143-0316.

出版信息

Pediatr Dermatol. 1994 Sep;11(3):204-8. doi: 10.1111/j.1525-1470.1994.tb00587.x.

Abstract

The risk of small congenital melanocytic nevi (CMN) developing into melanoma is not known, but is highly controversial. The frequency of small CMN is, paradoxically, slightly higher in some populations, such as blacks, who are at a lower risk of developing melanoma than whites. An estimate of the risk of malignant transformation of CMN in such a low-risk population could help in the management of congenital nevi in these patients and might also shed light on the inherent malignant risk of small CMN. We used a national population-based cancer registry, the Surveillance, Epidemiology, and End Results program (SEER), and the incidence of CMN in blacks taken from published newborn surveys to calculate a risk of malignant transformation. We calculated a maximum risk using a model based on a worst-case scenario, assuming that all melanomas on glabrous skin arise in CMN. We also calculated a modified risk based on the known historical association of nevi and melanomas in blacks, and estimates of the histologic association of the two. The cumulative maximum risk of malignant transformation in blacks to age 75 years was 1 in 164. It was strongly age dependent, with the majority occurring in persons over age 45. The estimated maximum risk before age 15 was less than 1 in 10,000 CMN, and in blacks age 15 to 35 less than 1 in 3700 CMN. The modified risk suggests that the worst-case scenario overestimates the risk by at least a factor of 12, making the actual risk in blacks up to age 75 approximately 1 in 2000.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

小先天性黑素细胞痣(CMN)发展为黑色素瘤的风险尚不清楚,但极具争议性。矛盾的是,小CMN的发生率在某些人群中略高,比如黑人,而黑人患黑色素瘤的风险低于白人。估计低风险人群中CMN恶变的风险有助于对这些患者的先天性痣进行管理,也可能有助于了解小CMN的内在恶变风险。我们使用了基于全国人口的癌症登记处——监测、流行病学和最终结果计划(SEER),以及从已发表的新生儿调查中获取的黑人CMN发病率来计算恶变风险。我们使用基于最坏情况的模型计算了最大风险,假设所有无毛皮肤上的黑色素瘤都起源于CMN。我们还根据黑人痣与黑色素瘤已知的历史关联以及两者的组织学关联计算了修正风险。黑人到75岁时恶变的累积最大风险为1/164。它强烈依赖于年龄,大多数发生在45岁以上的人群中。15岁之前估计的最大风险低于1/10000个CMN,15至35岁的黑人中低于1/3700个CMN。修正后的风险表明,最坏情况高估了风险至少12倍,使得黑人到75岁时的实际风险约为1/2000。(摘要截断于250字)

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