Wang Yuxiong, Wang Yuantao, Feng Mingliang, Lian Xin, Lei Yongsheng, Zhou Honglan
The Second Department of Urology, The First Hospital of Jilin University, Changchun, Jilin, China.
J Int Med Res. 2020 Oct;48(10):300060520942095. doi: 10.1177/0300060520942095.
Renal cell carcinoma (RCC) associated with Xp11.2 translocation/transcription factor E3 () gene fusion is a rare and independent subtype of RCC included in the classification of MiT (microphthalmia-associated transcriptional factor) family translocation RCC. Herein, we report an adult case of Xp11.2 translocation RCC, and review the relevant literature to improve our understanding of the pathogenesis, epidemiology, clinical manifestations, diagnosis, differential diagnosis, treatment, and other aspects of the disease.
与Xp11.2易位/转录因子E3(TFE3)基因融合相关的肾细胞癌(RCC)是RCC中一种罕见的独立亚型,被纳入MiT(小眼相关转录因子)家族易位性RCC分类中。在此,我们报告1例成人Xp11.2易位性RCC病例,并复习相关文献以增进我们对该疾病的发病机制、流行病学、临床表现、诊断、鉴别诊断、治疗及其他方面的认识。