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首页> 外文期刊>American Journal of Surgical Pathology >Molecular confirmation of t(6;11)(p21;q12) renal cell carcinoma in archival paraffin-embedded material using a break-apart TFEB FISH assay expands its clinicopathologic spectrum
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Molecular confirmation of t(6;11)(p21;q12) renal cell carcinoma in archival paraffin-embedded material using a break-apart TFEB FISH assay expands its clinicopathologic spectrum

机译:使用分离式TFEB FISH分析对档案石蜡包埋材料中的t(6; 11)(p21; q12)肾细胞癌进行分子确认,可扩展其临床病理学范围

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A subset of renal cell carcinomas (RCCs) is characterized by t(6;11)(p21;q12), which results in fusion of the untranslated Alpha (MALAT1) gene to the TFEB gene. Only 21 genetically confirmed cases of t(6;11) RCCs have been reported. This neoplasm typically demonstrates a distinctive biphasic morphology, comprising larger epithelioid cells and smaller cells clustered around basement membrane material; however, the full spectrum of its morphologic appearances is not known. The t(6;11) RCCs differ from most conventional RCCs in that they consistently express melanocytic immunohistochemical (IHC) markers such as HMB45 and Melan A and the cysteine protease cathepsin K but are often negative for epithelial markers such as cytokeratins. TFEB IHC has been proven to be useful to confirm the diagnosis of t(6;11) RCCs in archival material, because native TFEB is upregulated through promoter substitution by the gene fusion. However, IHC is highly fixation dependent and has been proven to be particularly difficult for TFEB. A validated fluorescence in situ hybridization (FISH) assay for molecular confirmation of the t(6;11) RCC in archival formalin-fixed, paraffin-embedded material has not been previously reported. We report herein the development of a break-apart TFEB FISH assay for the diagnosis of t(6;11)(p21;q12) RCCs. We validated the assay on 4 genetically confirmed cases and 76 relevant expected negative control cases and used the assay to report 8 new cases that expand the clinicopathologic spectrum of t(6;11) RCCs. An additional previously reported TFEB IHC-positive case was confirmed by TFEB FISH in 46-year-old archival material. In conclusion, TFEB FISH is a robust, clinically validated assay that can confirm the diagnosis of t(6;11) RCC in archival material and should allow a more comprehensive clinicopathologic delineation of this recently recognized neoplastic entity.
机译:肾细胞癌(RCC)的一个子集的特征是t(6; 11)(p21; q12),这导致未翻译的Alpha(MALAT1)基因与TFEB基因融合。仅报告了21例经遗传学证实的t(6; 11)RCC病例。这种肿瘤通常表现出独特的双相形态,包括较大的上皮样细胞和聚集在基膜材料周围的较小细胞。然而,其形态学表现的全谱尚不清楚。 t(6; 11)RCC与大多数常规RCC的不同之处在于,它们始终表达黑素细胞免疫组织化学(IHC)标记(例如HMB45和Melan A)和半胱氨酸蛋白酶组织蛋白酶K,但通常对上皮标记(例如细胞角蛋白)呈阴性。事实证明,TFEB IHC可用于确认档案材料中t(6; 11)RCC的诊断,因为天然TFEB通过基因融合的启动子取代而上调。但是,IHC高度依赖固定,并且已证明对于TFEB特别困难。先前尚未报道过用于分子福尔马林固定,石蜡包埋的材料中t(6; 11)RCC分子鉴定的经过验证的荧光原位杂交(FISH)实验。我们在本文中报告了用于诊断t(6; 11)(p21; q12)RCC的分离式TFEB FISH检测方法的开发。我们对4例经遗传学确诊的病例和76例相关的预期阴性对照病例进行了验证,并使用该方法报告了8例新的病例,这些病例扩大了t(6; 11)RCC的临床病理学范围。 TFEB FISH在46岁的档案材料中证实了另一例先前报道的TFEB IHC阳性病例。总之,TFEB FISH是一种可靠的,经过临床验证的测定方法,可以确认档案材料中t(6; 11)RCC的诊断,并且应该可以对该新近认识的赘生物进行更全面的临床病理学描述。

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