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首页> 外文期刊>American Journal of Surgical Pathology >Utilization of a TFE3 break-apart FISH assay in a renal tumor consultation service
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Utilization of a TFE3 break-apart FISH assay in a renal tumor consultation service

机译:TFE3断裂FISH检测在肾肿瘤咨询服务中的应用

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Xp11 translocation renal cell carcinomas (RCCs) are characterized by chromosome translocations involving the Xp11.2 breakpoint, resulting in gene fusions involving the TFE3 transcription factor. In archival material, the diagnosis can often be confirmed by TFE3 immunohistochemistry (IHC), but variable fixation (especially prevalent in consultation material) can lead to equivocal results. A TFE3 break-apart fluorescence in situ hybridization (FISH) assay has been developed to detect TFE3 gene rearrangements; however, the utility of this assay in a renal tumor consultation practice has not been examined. We reviewed 95 consecutive renal tumor consultation cases submitted to rule in or rule out Xp11 translocation RCC. Thirty-one cases were positive for TFE3 rearrangements by FISH. Patients ranged from 6 to 67 years of age (mean=30 y; median=28 y). Novel or distinctive morphologic features of these cases included extensive cystic change simulating multilocular cystic RCC (3 cases), sarcomatoid transformation (3 cases), oncocytic areas mimicking oncocytoma (1 case), trabecular architecture mimicking a carcinoid tumor (1 case), colonization of renal pelvic urothelium mimicking urothelial carcinoma in situ (1), and focal desmin and diffuse racemase immunoreactivity (1 case each). Twenty-six of the 31 TFE3 FISH-positive RCCs were unequivocally positive for TFE3 by IHC, but 4 were equivocal, and 1 was negative. Of the 64 cases that were negative by TFE3 FISH, 50 were negative by TFE3 IHC, and 14 were equivocal. Thirty-two of the 64 TFE3 FISH-negative cases could be classified into other accepted RCC subtypes: 23 as clear cell RCC, 5 as papillary RCC, 3 as clear cell papillary RCC, and 1 as chromophobe RCC. The other 32 cases remained unclassified, including 3 cathepsin K-positive RCC that closely resembled Xp11 translocation RCC. In conclusion, TFE3 FISH is highly useful in renal tumor consultation material, often resolving cases with equivocal TFE3 IHC results. Given the difficulty of optimizing TFE3 IHC, TFE3 FISH is for most laboratories the optimal test for establishing the diagnosis of Xp11 translocation RCC.
机译:Xp11易位性肾细胞癌(RCC)的特征是涉及Xp11.2断裂点的染色体易位,导致涉及TFE3转录因子的基因融合。在档案材料中,诊断通常可以通过TFE3免疫组织化学(IHC)进行确认,但是固定方式不固定(尤其是在咨询材料中普遍存在)可能导致模棱两可的结果。已经开发出TFE3断裂荧光原位杂交(FISH)检测法来检测TFE3基因重排。然而,该方法在肾肿瘤咨询实践中的实用性尚未得到检验。我们回顾了提交或排除Xp11易位RCC的95例连续性肾脏肿瘤咨询病例。 FISH对TFE3重排的31例阳性。患者年龄在6至67岁之间(平均= 30岁;中位数= 28岁)。这些病例的新颖或独特的形态学特征包括:广泛的囊性变化,模拟多房性RCC(3例),肉瘤样转变(3例),模仿肿瘤细胞瘤的吞噬区(1例),模仿类癌的小梁结构(1例),肾盂尿路上皮模仿原位尿路上皮癌(1),局灶性结节和弥漫消旋消旋酶免疫反应(各1例)。 IHC对TFE3阳性的31个TFE3 FISH阳性RCC中有26个明确阳性,但4个模棱两可,而1个阴性。在TFE3 FISH阴性的64例病例中,TFE3 IHC阴性的50例,模棱两可的14例。在64例TFE3 FISH阴性病例中,有32例可分为其他公认的RCC亚型:透明细胞RCC 23例,乳头状RCC 5例,透明细胞乳头RCC 3例,发色团RCC 1例。其他32例仍未分类,包括3个组织蛋白酶K阳性RCC,与Xp11易位RCC非常相似。总之,TFE3 FISH在肾肿瘤咨询材料中非常有用,通常可以解决TFE3 IHC结果不明确的病例。鉴于优化TFE3 IHC的困难,对于大多数实验室而言,TFE3 FISH是建立Xp11易位RCC诊断的最佳测试。

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