首页> 外文期刊>The Journal of dermatology >Histogenesis of cutaneous malignant melanoma: The vast majority do not develop from melanocytic nevus but arise de novo as melanoma in situ
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Histogenesis of cutaneous malignant melanoma: The vast majority do not develop from melanocytic nevus but arise de novo as melanoma in situ

机译:皮肤恶性黑素瘤的组织血肿:绝大多数不会从黑素核糖痣中发展,但由于黑色素瘤原位出现德诺伊

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It has been considered that most cutaneous malignant melanomas arise from pre-existing melanocytic nevus. Many clinical and histopathological studies seem to support this concept. Dysplastic nevus originally proposed by Clark's group is a key entity of the intermediate lesion between benign nevus and melanoma. The latest edition of the WHO Classification of Skin Tumours (2018) has excluded Clark nevus (dysplastic nevus of mild atypia) from dysplastic nevus, the latter being now classified into the low- and high-grade by the degrees of nuclear atypia. The World Health Organization classification regards dysplastic nevus of both grades as the intermediate lesion between common acquired nevus and the radial growth-phase melanoma. An extensive genetic study recently performed by Bastian's group indicated the existence of intermediate lesions between nevus and melanoma. In spite of these findings, some investigators doubt the concept of the intermediate lesions including dysplastic nevus and insist that the majority of melanomas arise de novo as melanoma in situ, not in association with a preceding nevus. The concept of de novo genesis of melanoma may be supported by a recent meta-analysis study revealing that 71% of melanomas likely arose de novo and 29% from pre-existing nevus. In this review article, from the viewpoint of de novo genesis of melanoma, the author critically discusses the relevant findings of melanoma genesis and proposes a new framework to interpret the morphological and genetic data alternatively. Clarification of the oncogenic process of melanoma has great impact not only on clinical dermatology but also on basic oncology.
机译:已被认为是大多数皮肤恶性黑色素由预先存在的黑素细胞痣产生。许多临床和组织病理学研究似乎都支持这一概念。克拉克集团最初提出的消化性痣是良性痣和黑素瘤之间中间病变的关键实体。最新版本的皮肤肿瘤分类(2018年)从消化不良痣中排除了克拉克痣(轻型Atypia的发育不良痣),后者现在被核原型的程度分为低级和高等级。世界卫生组织的分类至关重要,作为常见的痣与径向生长相黑素瘤之间的中间病变。最近由巴斯蒂安集团进行的广泛遗传研究表明,痣和黑色素瘤之间的中间病变存在。尽管有了这些发现,一些调查人员怀疑中间病变的概念,包括发育不良痣,并坚持大多数黑色素瘤出现为黑色素瘤原位,不与前面的痣结合。最近的Meta分析研究可以支持对黑色素瘤的Novo Genesis的概念,揭示了71%的黑色素可能来自诺维斯,从预先存在的痣中产生29%。在这篇审查文章中,从对黑色素瘤的Novo Genesis的角度来看,作者批判性地讨论了黑色素瘤创世纪的相关结果,并提出了一种替代地解释形态和遗传数据的新框架。澄清黑色素瘤的致癌过程不仅对临床皮肤病学产生了很大的影响,而且对碱性肿瘤有很大影响。

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