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NONO-TFE3 双重融合 FISH 检测作为 NONO-TFE3 肾细胞癌诊断工具的适用性。

The suitability of NONO-TFE3 dual-fusion FISH assay as a diagnostic tool for NONO-TFE3 renal cell carcinoma.

机构信息

Department of Urology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing, 210008, Jiangsu, China.

Department of Urology, Drum Tower Clinical Medical School of Nanjing Medical University, Nanjing, Jiangsu, China.

出版信息

Sci Rep. 2020 Oct 1;10(1):16361. doi: 10.1038/s41598-020-73309-4.

Abstract

NONO-TFE3 RCC is a subtype of Xp11.2 translocation renal cell carcinoma (RCC). So far, only a small amount of NONO-TFE3 RCC have been reported owing to lack of effective diagnosis methods. Utilizing the novel dual-fusion fluorescence in situ hybridization (FISH) probe reported here, 5 cases of NONO-TFE3 RCC were identified and were ultimately confirmed by RT-PCR. Histopathology, all 5 cases were consisted by sheets of epithelial cells and papillary architecture. The cytoplasm was abundantly clear, and nucleoli was not prominent. Besides, the nuclear palisading, subnuclear vacuoles and psammoma bodies were identified. The most distinctive features were strong positive TFE3 staining but equivocal split signals of the TFE3 probe, which might lead to the misdiagnosis of Xp11.2 translocation RCC. The median age and median tumor size of the five patients were 41.2 years and 3.6 cm, respectively. A median following follow-up of 27 months showed moderate disease progression and prognosis in NONO-TFE3 RCC patients. In conclusion, the present study demonstrates the effectiveness and reliability of the NONO-TFE3 dual-fusion FISH probe for diagnosing NONO-TFE3 RCC. Suspected cases of Xp11.2 translocation RCC showing biphasic pattern, strong positive TFE3 staining, and equivocal split signals in the TFE3 FISH assay indicated a possibility of NONO-TFE3 RCC.

摘要

NONO-TFE3 RCC 是 Xp11.2 易位肾细胞癌(RCC)的一种亚型。由于缺乏有效的诊断方法,到目前为止,仅报道了少量的 NONO-TFE3 RCC。利用本研究报告的新型双融合荧光原位杂交(FISH)探针,鉴定了 5 例 NONO-TFE3 RCC,并最终通过 RT-PCR 得到证实。组织病理学上,所有 5 例均由片状上皮细胞和乳头状结构组成。细胞质丰富透明,核仁不明显。此外,还观察到核栅状、核下空泡和砂粒体。最显著的特征是 TFE3 染色强阳性,但 TFE3 探针的分裂信号不确定,这可能导致 Xp11.2 易位 RCC 的误诊。5 名患者的中位年龄和肿瘤大小分别为 41.2 岁和 3.6cm。中位随访 27 个月显示 NONO-TFE3 RCC 患者的疾病进展和预后中等。总之,本研究表明 NONO-TFE3 双融合 FISH 探针诊断 NONO-TFE3 RCC 的有效性和可靠性。疑似 Xp11.2 易位 RCC 表现为双相模式、TFE3 染色强阳性和 TFE3 FISH 检测中不确定的分裂信号,提示可能为 NONO-TFE3 RCC。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa64/7530984/b57c595880e7/41598_2020_73309_Fig1_HTML.jpg

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