Brunelli Matteo, Eble John N, Zhang Shaobo, Martignoni Guido, Delahunt Brett, Cheng Liang
Department of Pathology and Laboratory Medicine, Universitá di Verona, Verona, Italy.
Mod Pathol. 2005 Feb;18(2):161-9. doi: 10.1038/modpathol.3800286.
That chromophobe renal cell carcinoma has an uncommon eosinophilic variant has been recognized for more than a decade. In sections stained with hematoxylin and eosin, the eosinophilic variant of chromophobe renal cell carcinoma and renal oncocytoma are similar in appearance. While it is well established that chromophobe renal cell carcinoma and renal oncocytoma have different patterns of genetic anomalies, little is known of the genetics of the eosinophilic variant of chromophobe renal cell carcinoma. This study was undertaken to elucidate the genetic lesions of eosinophilic chromophobe renal cell carcinoma and to compare them with those found in classic chromophobe renal cell carcinoma and in renal oncocytoma. A total of 29 renal neoplasms--nine eosinophilic chromophobe renal cell carcinomas, 10 classic chromophobe renal cell carcinomas, and 10 oncocytomas--were investigated by fluorescence in situ hybridization on 5 microm paraffin-embedded tissue sections with centromeric probes for chromosomes 1, 2, 6, 10, and 17. Signals were counted in 100-200 neoplastic nuclei from each tumor. Chromophobe renal cell carcinomas frequently showed loss of chromosomes 1 (70% of classic, 67% of eosinophilic), 2 (90% classic, 56% eosinophilic), 6 (80% classic, 56% eosinophilic), 10 (60% classic, 44% eosinophilic), and 17 (90% classic, 78% eosinophilic); Among the classic chromophobe renal cell carcinomas, only one had no loss of any of the chromosomes, while 50% had loss of all five chromosomes. Among the eosinophilic chromophobe renal cell carcinomas, one of nine had no loss and 44% had loss of all five chromosomes. One oncocytoma had loss of chromosome 1. No other chromosomal loss was detected in the oncocytomas. In conclusion, losses of chromosomes 1, 2, 6, 10, and 17 are frequent in both eosinophilic and classic chromophobe renal cell carcinomas. Loss of chromosome 1 occurs occasionally in oncocytoma but losses of chromosomes 2, 6, 10, and 17 are not found in oncocytomas. When the differential diagnostic problem is oncocytoma vs eosinophilic chromophobe renal cell carcinoma, detection of losses of chromosomes 2, 6, 10, or 17 effectively excludes the diagnosis of oncocytoma and supports the diagnosis of chromophobe renal cell carcinoma.
十多年来,人们已经认识到嫌色肾细胞癌存在一种罕见的嗜酸性变体。在苏木精和伊红染色切片中,嫌色肾细胞癌的嗜酸性变体和肾嗜酸细胞瘤在外观上相似。虽然已经明确嫌色肾细胞癌和肾嗜酸细胞瘤有不同的基因异常模式,但对于嫌色肾细胞癌嗜酸性变体的遗传学知之甚少。本研究旨在阐明嗜酸性嫌色肾细胞癌的基因损伤,并将其与经典嫌色肾细胞癌和肾嗜酸细胞瘤中的基因损伤进行比较。通过对5微米厚的石蜡包埋组织切片进行荧光原位杂交,使用针对染色体1、2、6、10和17的着丝粒探针,对总共29例肾肿瘤进行了研究,其中包括9例嗜酸性嫌色肾细胞癌、10例经典嫌色肾细胞癌和10例嗜酸细胞瘤。对每个肿瘤的100 - 200个肿瘤细胞核中的信号进行计数。嫌色肾细胞癌经常出现染色体1(经典型70%,嗜酸性型67%)、2(经典型90%,嗜酸性型56%)、6(经典型80%,嗜酸性型56%)、10(经典型60%,嗜酸性型44%)和17(经典型90%,嗜酸性型78%)的缺失;在经典嫌色肾细胞癌中,只有1例没有任何染色体缺失,而50%的病例所有5条染色体均缺失。在嗜酸性嫌色肾细胞癌中,9例中有1例没有缺失,44%的病例所有5条染色体均缺失。1例嗜酸细胞瘤出现染色体1缺失。在嗜酸细胞瘤中未检测到其他染色体缺失。总之,染色体1、2、6、10和17的缺失在嗜酸性和经典嫌色肾细胞癌中都很常见。染色体1的缺失偶尔出现在嗜酸细胞瘤中,但染色体2、6、10和17的缺失在嗜酸细胞瘤中未发现。当鉴别诊断问题是嗜酸细胞瘤与嗜酸性嫌色肾细胞癌时,检测染色体2、6、10或17的缺失可有效排除嗜酸细胞瘤的诊断,并支持嫌色肾细胞癌的诊断。