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

Pathologie (Heidelberg, Germany) Pub Date : 2025-02-01 Epub Date: 2024-12-30 DOI:10.1007/s00292-024-01409-3
Abbas Agaimy, Arndt Hartmann
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引用次数: 0

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.

【未分化和去分化肾细胞癌:形态分子方面和鉴别诊断的最新进展】。
在过去的二十年中,各种肾细胞癌(RCCs)的组织学亚型发生了重大变化。这导致引入了一些新的表型和基因定义的实体,其中许多也被列入世卫组织目前的分类。在某些情况下,这些定义明确的实体中的一些可能经历去分化过程,导致其表型和免疫组织化学特征的丧失,从而采用不可描述的间变性形态。因此,最初定义实体的肿瘤克隆要么完全生长过度而丢失,要么只是在对肿瘤进行采样时遗漏。这最后一种常见的去分化途径导致了几个肿瘤学上的缺点,并阻碍了针对组织学的系统性治疗方法。此外,如SDH-和fh缺陷的RCC,如果不可能准确分型,遗传癌症的可能性很容易被忽视。本文概述了可能经历去分化的主要RCC亚型及其鉴别诊断方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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