Department of Pathology, The University of Chicago, IL, 60605, USA.
Department of Pathology, The University of Chicago, IL, 60605, USA.
Hum Pathol. 2023 Apr;134:124-133. doi: 10.1016/j.humpath.2022.12.015. Epub 2022 Dec 30.
The 2016 World Health Organization (WHO) Classification of Tumors of the Urinary System includes renal cell carcinoma (RCC) with leiomyomatous stroma (RCC-LS) as a provisional category. Recent studies have shown that this category includes at least 4 subtypes: clear cell (CCRCC), clear cell papillary renal cell tumor (CCPRCT), ELOC (TCEB1) mutated, and a subtype of RCC with TSC/MTOR mutations. The most recent 2022 World Health Organization (WHO) Classification of Tumors of the Urinary System includes ELOC mutated RCC-LS as a distinct entity but does not address any other renal tumors with smooth muscle stroma. We reviewed >500 cases of RCC with clear cell phenotype and identified 12 cases that exhibited prominent smooth muscle stroma, of which 4 of the cases had been previously reported. Review of the H&E revealed that all of the tumors were circumscribed with nested, solid, tubular, and tubulopapillary architecture. The epithelium was intimately embedded in the rich smooth muscle stroma. WHO/ISUP grade corresponded to grade 3 and 4. Nuclei were randomly distributed and the cytoplasm had predominantly clear and occasionally flocculent appearance. Immunohistochemically, all the cases showed membranous CAIX staining, although the pattern was combined cup and box-shaped. CK7 was positive in all cases ranging from 25% to 100% of cells. Membranous and apical staining of CD10 was present in all cases. Next generation sequencing (NGS) of these cases identified mutations in TSC1 (n = 4), TSC2 (n = 3), and MTOR (n = 4) with one case exhibiting loss of TSC1. This descriptive study, although small, demonstrates the difficulty in applying the current WHO provisional criteria at a single institution. Given the heterogeneity seen with these cases, we suggest following up an immunohistochemical panel of CAIX, CK7, and CD10 with molecular diagnostic studies to assist in the diagnosis of TSC/MTOR associated RCC-LS, which we believe is a distinct entity.
2016 年世界卫生组织(WHO)泌尿系统肿瘤分类将具有平滑肌基质的肾细胞癌(RCC-LS)作为一个临时类别。最近的研究表明,该类别至少包括 4 个亚型:透明细胞(CCRCC)、透明细胞乳头状肾细胞肿瘤(CCPRCT)、ELOC(TCEB1)突变型和 TSC/MTOR 突变型 RCC 亚型。最近的 2022 年世界卫生组织(WHO)泌尿系统肿瘤分类将 ELOC 突变型 RCC-LS 作为一个独立实体,但未涉及任何其他具有平滑肌基质的肾肿瘤。我们回顾了>500 例具有透明细胞表型的 RCC 病例,发现 12 例具有明显的平滑肌基质,其中 4 例先前有报道。对 H&E 的回顾显示,所有肿瘤均呈边界清楚的巢状、实性、管状和管状乳头状结构。上皮细胞紧密嵌入丰富的平滑肌基质中。WHO/ISUP 分级对应于 3 级和 4 级。核随机分布,细胞质主要呈透明状,偶尔呈絮状。免疫组化染色显示,所有病例均显示膜 CAIX 染色,尽管模式为杯状和盒状结合。所有病例 CK7 均呈阳性,阳性细胞比例为 25%至 100%。所有病例均存在 CD10 的膜和顶染。对这些病例的下一代测序(NGS)发现 TSC1(n=4)、TSC2(n=3)和 MTOR(n=4)突变,其中 1 例存在 TSC1 缺失。虽然本研究规模较小,但证明了在单一机构应用当前 WHO 临时标准的困难。鉴于这些病例的异质性,我们建议对 CAIX、CK7 和 CD10 的免疫组化面板进行分子诊断研究,以协助诊断 TSC/MTOR 相关的 RCC-LS,我们认为这是一个独立的实体。