Whiteman D C, Valery P, McWhirter W, Green A C
Epidemiology and Population Health Unit, Queensland Institute of Medical Research, P.O. Royal Brisbane Hospital, Herston, Australia.
Int J Cancer. 1997 Jan 6;70(1):26-31. doi: 10.1002/(sici)1097-0215(19970106)70:1<26::aid-ijc4>3.0.co;2-8.
The causes of cutaneous melanoma among children under 15 years are largely unknown. We report the findings of an epidemiological study of childhood melanoma in Queensland, Australia, which has the highest incidence rates in the world. All 61 cases of melanoma in children less than 15 years notified to the Queensland Cancer Registry 1987-1994 were eligible to participate in a population-based, case-control study. Data were collected through structured, face-to-face interviews with parents and skin examinations of the 52 participating cases and 156 age- and sex-matched controls. The strongest determinants of melanoma risk found among Queensland children were constitutional factors, including the presence of more than 10 naevi greater than 5 mm in diameter (RR 9.9, 95% CI 2.5-38.9), heavy facial freckling (RR 6.4, 95% CI 1.9-21.6), an inability to tan on exposure to the sun (RR 8.8, 95% CI 2.1-36.2) and a family history of melanoma (RR 4.2, 95% CI 1.9-9.3). These factors remained significantly associated with melanoma after adjusting for other risk factors. No measures of acute or chronic exposure to solar UV radiation were associated with childhood melanoma in our study. Established risk factors, including giant congenital naevi and xeroderma pigmentosum, were not present among any of the children in the study. Melanoma in childhood appears to have similar epidemiologic characteristics to the adult form of the disease, being associated with a cluster of phenotypic attributes indicating cutaneous sensitivity to the effects of sun exposure. Our findings support the contention that childhood melanoma occurs in susceptible individuals with a low threshold for pigment cell tumorigenesis. From a public-health perspective, children at elevated risk for melanoma can be identified on the basis of phenotype and family history.
15岁以下儿童患皮肤黑色素瘤的原因在很大程度上尚不清楚。我们报告了一项对澳大利亚昆士兰州儿童黑色素瘤的流行病学研究结果,该州是世界上发病率最高的地区。1987年至1994年向昆士兰州癌症登记处报告的所有61例15岁以下儿童黑色素瘤病例均有资格参与一项基于人群的病例对照研究。通过与家长进行结构化的面对面访谈以及对52名参与研究的病例和156名年龄及性别匹配的对照进行皮肤检查来收集数据。在昆士兰州儿童中发现的黑色素瘤风险最强的决定因素是体质因素,包括存在10个以上直径大于5毫米的痣(相对危险度9.9,95%可信区间2.5 - 38.9)、面部重度雀斑(相对危险度6.4,95%可信区间1.9 - 21.6)、日晒后无法晒黑(相对危险度8.8,95%可信区间2.1 - 36.2)以及黑色素瘤家族史(相对危险度4.2,95%可信区间1.9 - 9.3)。在对其他风险因素进行调整后,这些因素仍与黑色素瘤显著相关。在我们的研究中,没有任何急性或慢性暴露于太阳紫外线辐射的指标与儿童黑色素瘤相关。研究中的任何儿童均不存在已确定的风险因素,包括巨大先天性痣和着色性干皮病。儿童黑色素瘤似乎具有与成人形式的疾病相似的流行病学特征,与一系列表明皮肤对日晒影响敏感的表型特征相关。我们的研究结果支持这样的观点,即儿童黑色素瘤发生在对色素细胞肿瘤发生阈值较低的易感个体中。从公共卫生的角度来看,可以根据表型和家族史识别出黑色素瘤风险较高的儿童。