Department of Pathology, Shanghai Jiaotong University Medical School Affiliated Ruijin Hospital, Number 197, Ruijin Er Road, Huangpu District, Shanghai, China.
Virchows Arch. 2024 Aug;485(2):379-382. doi: 10.1007/s00428-023-03667-7. Epub 2023 Dec 16.
Renal cell carcinoma with fibromyomatous stroma (RCC FMS), defined as an "emerging entity" in the 2016 WHO classification and recommended to be a novel entity by GUPS, is represented by tumor cells with clear to mildly eosinophilic cytoplasm displaying elongated and branching tubules and papillae. A fibromyomatous stroma could be observed in these tumors. These tumors are immunopositive for CK7 and featured by ELOC and/or TSC/mTOR gene mutations. In the 2022 WHO classification, ELOC mutated RCC is classified as a molecularly defined RCCs as an individual renal entity. However, there are limited descriptions of TSC/mTOR alterations in RCC FMS. Herein, we reported a case of 28-year-old woman with RCC FMS with intact ELOC and TSC/mTOR genes but ASXL1 mutation. The tumor cells were positive for mTOR expression. This case may indicate that altered mTOR expression, but not limited to mutated TSC/mTOR gene, that participates in the pathogenesis of RCC FMS.
肾细胞癌伴纤维平滑肌基质(RCC FMS),在 2016 年 WHO 分类中被定义为“新兴实体”,并被 GUPS 推荐为一种新实体,其特征是肿瘤细胞具有清晰至轻度嗜酸性胞浆,呈拉长的分支状小管和乳头。在这些肿瘤中可以观察到纤维平滑肌基质。这些肿瘤对 CK7 呈免疫阳性,并具有 ELOC 和/或 TSC/mTOR 基因突变。在 2022 年 WHO 分类中,ELOC 突变型 RCC 被归类为分子定义的 RCCs,作为一种独立的肾实体。然而,关于 RCC FMS 中 TSC/mTOR 改变的描述有限。在此,我们报告了一例 28 岁女性 RCC FMS 病例,其 ELOC 和 TSC/mTOR 基因完整,但存在 ASXL1 突变。肿瘤细胞对 mTOR 表达呈阳性。该病例可能表明,改变的 mTOR 表达,而不仅仅是突变的 TSC/mTOR 基因,参与了 RCC FMS 的发病机制。