Departments of Pathology.
Oncology.
Am J Surg Pathol. 2023 Nov 1;47(11):1267-1273. doi: 10.1097/PAS.0000000000002117. Epub 2023 Sep 4.
Renal cell carcinoma with fibromyomatous stroma (RCCFMS) include ELOC/TCEB1 -mutated renal cell carcinoma (RCC) and those with TSC1/2 / MTOR alterations. Besides morphologic similarity, most of these tumors is known to be diffusely positive for carbonic anhydrase IX and cytokeratin 7 by immunohistochemistry. We previously showed strong and diffuse expression of GPNMB (glycoprotein nonmetastatic B) in translocation RCC and eosinophilic renal neoplasms with known TSC1/2/MTOR alterations. We retrospectively identified molecularly confirmed cases of TCEB1/ELOC -mutated RCC (7 tumors from 7 patients), and RCCFMS with alterations in TSC1/2/MTOR (6 tumors from 5 patients, 1 patient with tuberous sclerosis syndrome). In addition, we included 7 clear cell papillary renal cell tumors (CCPRCTs) and 8 clear cell RCC, as they can also present morphologic overlap with RCCFMS. Morphologically, RCCs with TSC1/2/MTOR alterations and those with TCEB1/ELOC mutations were indistinguishable and characterized by papillary, nested, or tubular architecture, with tumor cells with clear cytoplasm and low nuclear grade. By immunohistochemistry, cytokeratin 7 was positive in 5/7 (71%) of TCEB1/ELOC -mutated RCCs, 6/6 (100%) of RCCs with TSC1/2/mTOR alterations, and 7/7 (100%) of CCPRCTs ( P =not significant). Carbonic anhydrase IX was positive in 7/7 TCEB1/ELOC -mutated RCCs, 6/6 (100%) of RCCs with TSC1/2/MTOR alterations, and 7/7 (100%) of CCPRCTs ( P =NS). GPNMB was strongly and diffusely positive in all tumors with TSC1/2/MTOR alterations (6/6), while negative in all TCEB1/ELOC -mutated RCCs (0/6), or CCPRCTs (0/7) ( P =0.002). Two of 8 clear cell RCC showed focal weak staining, while 6/8 were negative. In conclusion, the results support the use of GPNMB to distinguish RCCFMS with TSC1/2/MTOR alterations from others with similar morphology.
富含纤维肌瘤样基质的肾细胞癌(RCCFMS)包括 ELOC/TCEB1 突变型肾细胞癌(RCC)和 TSC1/2/MTOR 改变型 RCC。除了形态学上的相似性,这些肿瘤中的大多数通过免疫组织化学检测,已知为碳酸酐酶 IX 和细胞角蛋白 7 弥漫阳性。我们之前曾显示,在具有已知 TSC1/2/MTOR 改变的易位 RCC 和嗜酸性肾肿瘤中,GPNMB(糖蛋白非转移性 B)表达强烈且弥漫。我们回顾性鉴定了分子证实的 TCEB1/ELOC 突变型 RCC(7 例来自 7 例患者)和 TSC1/2/MTOR 改变的 RCCFMS(5 例患者中的 6 例,1 例患有结节性硬化症综合征)。此外,我们纳入了 7 例透明细胞乳头状肾细胞癌(CCPRCT)和 8 例透明细胞肾细胞癌,因为它们也可能与 RCCFMS 在形态上重叠。形态上,具有 TSC1/2/MTOR 改变的 RCC 和具有 TCEB1/ELOC 突变的 RCC 无法区分,其特征为乳头状、巢状或管状结构,肿瘤细胞具有透明细胞质和低核级。通过免疫组织化学,在 7/7(71%)例 TCEB1/ELOC 突变型 RCC 中,6/6(100%)例具有 TSC1/2/MTOR 改变的 RCC 中,以及 7/7(100%)例 CCPRCT 中,细胞角蛋白 7 阳性(P=无统计学意义)。在 7/7 例 TCEB1/ELOC 突变型 RCC 中,6/6(100%)例具有 TSC1/2/MTOR 改变的 RCC 中,以及 7/7 例 CCPRCT 中,碳酸酐酶 IX 阳性(P=无统计学意义)。GPNMB 在所有具有 TSC1/2/MTOR 改变的肿瘤中均强烈且弥漫阳性(6/6),而在所有 TCEB1/ELOC 突变型 RCC 中(0/6)或 CCPRCT 中(0/7)均为阴性(P=0.002)。8 例透明细胞肾细胞癌中有 2 例表现为局灶性弱阳性染色,而 6 例为阴性。总之,这些结果支持使用 GPNMB 来区分具有 TSC1/2/MTOR 改变的 RCCFMS 与具有相似形态的其他肿瘤。