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[未分化和去分化肾细胞癌:基于最新进展的形态分子学特征及鉴别诊断]

[Undifferentiated and dedifferentiated renal cell carcinomas : Morphomolecular aspects and differential diagnosis in light of recent developments].

作者信息

Agaimy Abbas, Hartmann Arndt

机构信息

Institut für Pathologie, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Krankenhausstraße 8-10, 91054, Erlangen, Deutschland.

出版信息

Pathologie (Heidelb). 2025 Feb;46(1):40-47. doi: 10.1007/s00292-024-01409-3. Epub 2024 Dec 30.

Abstract

Histological subtyping of diverse renal cell carcinomas (RCCs) has seen significant changes during the last two decades. This resulted in the introduction of several new phenotypically and genetically defined entities, many which are also listed in the current WHO classification. Some of these well-defined entities may, under certain circumstances, undergo a process of dedifferentiation resulting in loss of their phenotypic and immunohistochemical features, hence adopting a non-descript anaplastic morphology. Accordingly, the original entity-defining tumor clone might be either totally overgrown and lost or just be missed by sampling the tumor. This final common pathway of dedifferentiation results in several oncological disadvantages and prevents a histology-tailored approach to systemic therapy. In addition, the possibility of inherited cancer as in the case of SDH- and FH-deficient RCC would be easily overlooked if the exact subtyping is not possible. This overview article illuminates the main RCC subtypes that may undergo dedifferentiation and their differential diagnostic approach.

摘要

在过去二十年中,各种肾细胞癌(RCC)的组织学亚型分类发生了显著变化。这导致引入了几个新的表型和基因定义的实体,其中许多也列在当前的世界卫生组织分类中。在某些情况下,这些定义明确的实体中的一些可能会经历去分化过程,导致其表型和免疫组化特征丧失,从而呈现出无特征性的间变形态。因此,最初定义实体的肿瘤克隆可能会完全过度生长并消失,或者在对肿瘤进行取样时被遗漏。这种去分化的最终共同途径导致了几个肿瘤学上的不利因素,并阻碍了针对全身治疗的组织学定制方法。此外,如果无法进行准确的亚型分类,像SDH和FH缺陷型RCC那样的遗传性癌症的可能性很容易被忽视。这篇综述文章阐明了可能发生去分化的主要RCC亚型及其鉴别诊断方法。

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