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皮肤黑色素瘤的黑素细胞前体。估计风险及管理指南。

Melanocytic precursors of cutaneous melanoma. Estimated risks and guidelines for management.

作者信息

Rhodes A R

出版信息

Med Clin North Am. 1986 Jan;70(1):3-37. doi: 10.1016/s0025-7125(16)30966-x.

DOI:10.1016/s0025-7125(16)30966-x
PMID:3510347
Abstract

There are several recognizable melanocytic precursors of cutaneous melanoma. These precursors include lentigo maligna, dysplastic melanocytic nevi, congenital nevi (of any size), and darkly pigmented lesions of acral surfaces and mucous membranes. Lentigo maligna is an uncommon melanocytic dysplasia, present in 3 per 1000 individuals over the age of 50 years and accounting for 4 percent of all cutaneous melanomas. Dysplastic melanocytic nevi are present in 2 per cent of white adults, and may account for at least a fifth of cases of cutaneous melanoma. Congenital nevomelanocytic nevi are present in 1 per cent of newborns; the vast majority of congenital nevi are smaller than 3 to 4 cm in diameter, while very large congenital nevi are present in 1 in 20,000 to 1 in 500,000 newborns. Very large congenital nevi account for less than 0.1 percent of cutaneous melanomas, whereas small varieties of congenital nevi may account for 15 percent of cutaneous melanomas. If individuals with lentigo maligna live long enough, possibly a third to a half are said to develop melanoma. This figure may be biased high. Persons with dysplastic melanocytic nevi in the familial melanoma setting have an estimated lifetime risk of developing melanoma approaching 100 per cent. Persons with dysplastic melanocytic nevi in other settings may have a lifetime melanoma risk of 18 per cent. Persons with congenital nevi of any size may have a lifetime melanoma risk of at least 5 per cent. Early recognition of these precursor melanocytic tumors, particularly in high-risk individuals (i.e., those with a personal or family history of melanoma), and careful photographic follow-up or prophylactic excision of these lesions may be the most effective means of reducing the morbidity and mortality of cutaneous melanoma. The impact of routine screening and excision of presumed melanoma precursors is unknown. Clinical judgment is required to balance the theoretical risk of melanoma associated with a given precursor and the known risks of surgery and anesthesia for a given individual. It must be kept in mind that the vast majority of acquired melanocytic nevi in adults are harmless. Probably even the majority of dysplastic nevi and small congenital nevi will remain unchanged throughout life. The simple recognition of the existence of melanoma precursors will heighten suspicion for these lesions and raise awareness of the earliest signs of malignant change.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

皮肤黑色素瘤有几种可识别的黑素细胞前体。这些前体包括恶性雀斑样痣、发育异常性黑素细胞痣、先天性痣(任何大小)以及掌跖和黏膜的色素沉着较深的病变。恶性雀斑样痣是一种不常见的黑素细胞发育异常,在50岁以上人群中每1000人中有3人出现,占所有皮肤黑色素瘤的4%。发育异常性黑素细胞痣在2%的白人成年人中存在,可能占皮肤黑色素瘤病例的至少五分之一。先天性黑素细胞痣在1%的新生儿中存在;绝大多数先天性痣直径小于3至4厘米,而非常大的先天性痣在每20000至500000名新生儿中有1例。非常大的先天性痣占皮肤黑色素瘤的比例不到0.1%,而小的先天性痣可能占皮肤黑色素瘤的15%。如果患有恶性雀斑样痣的个体活得足够长,据说可能有三分之一到一半会发展为黑色素瘤。这个数字可能偏高。在家族性黑色素瘤背景下有发育异常性黑素细胞痣的个体,估计一生中患黑色素瘤的风险接近100%。在其他情况下有发育异常性黑素细胞痣的个体,一生中患黑色素瘤的风险可能为18%。任何大小的先天性痣患者一生中患黑色素瘤的风险可能至少为5%。早期识别这些黑素细胞前体肿瘤,特别是在高危个体(即有个人或家族黑色素瘤病史者)中,以及对这些病变进行仔细的摄影随访或预防性切除,可能是降低皮肤黑色素瘤发病率和死亡率的最有效方法。对假定的黑色素瘤前体进行常规筛查和切除的影响尚不清楚。需要临床判断来平衡与特定前体相关的黑色素瘤理论风险和特定个体已知的手术及麻醉风险。必须记住,成年人中绝大多数后天性黑素细胞痣是无害的。甚至可能大多数发育异常性痣和小的先天性痣在一生中都不会改变。简单认识到黑色素瘤前体的存在会增加对这些病变的怀疑,并提高对恶性变化最早迹象的认识。(摘要截选至400字)

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