Zaal L H, Mooi W J, Sillevis Smitt J H, van der Horst C M A M
Department of Plastic, Reconstructive and Hand Surgery, Isala Klinieken, Zwolle, The Netherlands.
Br J Plast Surg. 2004 Dec;57(8):707-19. doi: 10.1016/j.bjps.2004.04.022.
Congenital naevi (CN) vary greatly in size, macroscopic appearance and histology. There is a practical need to subdivide CN according to size, since size differences have a direct bearing on cosmetic and resultant psychological problems, and on therapeutic options, and probably on the chance of malignant transformation. In this review, we summarise the literature on size subgroupings of CN, with special focus on giant congenital naevi and their risk of malignant transformation.
A Medline literature search from 1966 to October 2002 was performed. Only English-language studies focusing on CN in association with melanoma were included. The final strategy consisted of textwords and medical subject heading (MeSH) terms on small, medium, large and giant congenital naevi combined with the textwords classification, histology and melanoma. Additional manual cross-referencing was performed. We excluded articles that dealt only with aspects of treatments.
A wide variety of criteria for size subgrouping of CN has been put forward in the literature and precludes a direct comparison of reported data (Table 1). We identified 35 such articles in the world literature in which no less than seven different definitions of minimum size of a giant CN were employed. Histologically, it is difficult or even impossible to conclude that a naevus is congenital or acquired, especially in case of a small lesion, since the differences are not absolute (Table 2). Giant CN have an increased risk for malignant transformation, but the reported incidence rates have differed widely from one to 31% (Table 3). Reported melanoma incidence rates have derived from retro- and prospective studies, reviews and case reports, and compared with each other using different definitions. On top of this, patients in different age groups were reported, who were registered in different referral centers.
To allow comparison of study results from different centers, it is essential that the size subclassification of CN is based on standard and generally accepted criteria. We recommend defining GCN as a CN covering one percent body surface area in face and neck and two percent elsewhere on the body. Based on a review of the world literature, we recommend prophylactic excision of all CN, in close communication with patient and family and individualising treatment accordingly.
先天性痣(CN)在大小、宏观外观和组织学上差异很大。根据大小对CN进行细分具有实际必要性,因为大小差异直接关系到美容及由此产生的心理问题、治疗选择,可能还关系到恶变几率。在本综述中,我们总结了关于CN大小亚组分类的文献,特别关注巨大先天性痣及其恶变风险。
进行了1966年至2002年10月的Medline文献检索。仅纳入聚焦于CN与黑色素瘤相关的英文研究。最终检索策略包括关于小、中、大及巨大先天性痣的文本词和医学主题词(MeSH),并结合文本词分类、组织学和黑色素瘤。还进行了额外的手动交叉引用。我们排除了仅涉及治疗方面的文章。
文献中提出了多种CN大小亚组分类标准,这使得所报道的数据难以直接比较(表1)。我们在世界文献中识别出35篇此类文章,其中对巨大CN的最小大小采用了不少于七种不同定义。从组织学上看,很难甚至不可能断定一个痣是先天性还是后天性的,尤其是对于小病变,因为差异并非绝对(表2)。巨大CN恶变风险增加,但所报道的发病率从1%到31%差异很大(表3)。所报道的黑色素瘤发病率来自回顾性和前瞻性研究、综述及病例报告,且使用不同定义相互比较。除此之外,报道的患者年龄组不同,且登记于不同的转诊中心。
为便于不同中心的研究结果进行比较,CN的大小亚分类必须基于标准且被普遍接受的标准。我们建议将巨大先天性痣定义为面部和颈部覆盖体表面积1%、身体其他部位覆盖2%的先天性痣。基于对世界文献的综述,我们建议与患者及其家属密切沟通并相应地个体化治疗,对所有先天性痣进行预防性切除。