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儿童Xp11.2易位/TFE3基因融合相关性肾癌的影像学表现
引用本文:彭飞,闫学强,邵剑波. 儿童Xp11.2易位/TFE3基因融合相关性肾癌的影像学表现[J]. 肿瘤防治研究, 2021, 48(9): 883-887. DOI: 10.3971/j.issn.1000-8578.2021.21.0786
作者姓名:彭飞  闫学强  邵剑波
作者单位:1. 430016 武汉,华中科技大学同济医学院附属武汉儿童医院普外科;2. 430016 武汉,华中科技大学同济医学院附属武汉儿童医院影像中心
摘    要:目的 探讨儿童Xp11.2易位/TFE3基因融合相关性肾癌(Xp11.2 tRCC)的影像学表现.方法 回顾性分析我院2015年1月-2020年12月经手术病理证实为Xp11.2 tRCC的5例患儿临床及影像学资料,其中4例行CT平扫及增强检查,1例行MRI平扫、增强及DWI检查.观察分析肿瘤的部位、大小、形态、边界、...

关 键 词:肾癌  Xp11.2易位  儿童  体层摄影术,X线计算机  磁共振成像
收稿时间:2021-07-06

Imaging Characteristics of Renal Cell Carcinoma Associated with Xp11.2 Translocation/TFE3 Gene Fusions in Children
PENG Fei,YAN Xueqiang,SHAO Jianbo. Imaging Characteristics of Renal Cell Carcinoma Associated with Xp11.2 Translocation/TFE3 Gene Fusions in Children[J]. Cancer Research on Prevention and Treatment, 2021, 48(9): 883-887. DOI: 10.3971/j.issn.1000-8578.2021.21.0786
Authors:PENG Fei  YAN Xueqiang  SHAO Jianbo
Affiliation:1. Department of General Surgery, Wuhan Children’s Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430016, China; 2. Medical Imaging Center, Wuhan Children’s Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430016, China
Abstract:Objective To investigate the imaging characteristics of renal cell carcinoma associated with Xp11.2 translocation/TFE3 gene fusion. Methods We retrospectively analyzed the clinical and imaging data of five children with Xp11.2 tRCC confirmed by surgery and pathology in our hospital from January 2015 to December 2020. Four cases underwent CT plain scan and contrast-enhanced examination, and one case underwent MRI plain scan, contrast-enhanced examination and DWI examination. We observed and analyzed the location, size, shape, boundary, composition, enhancement pattern and degree, the relation with the renal hilum and adjacent large vessels, and the metastasis of the tumor. Results All cases were cortical-medullary type. Four cases were solid/cystic-solid lesions, iso- or slightly hyper-density on CT scans with calcification and necrosis, in which a few with bleeding or cystic lesions. Enhanced scanning primarily showed mild to moderate enhancement, and enhancement of pseudocapsule was seen during the delayed phase. One case was cystic lesion, the cystic fluid presented as hypo-density on CT, and T1 hypo-intensity and T2 hyper-intensity, as well as restricted diffusion on DWI. No enhancement was found in the cystic part after enhancement. There were irregular and thickened cystic wall and septum, and mural nodules on enhanced MRI. Conclusion Several characteristics of Xp11.2 tRCC in children could be drawn. Punctate and patchy calcifications in or around the solid/cystic-solid lesions and delayed “pseudocapsule sign” are typical. The possibility of Xp11.2 tRCC should be considered when there are irregular and thickened cystic wall and septum and the enhancement of mural nodules.
Keywords:Renal cell carcinoma  Xp11.2 translocation  Children  Tomography   X-ray computer  Magnetic resonance imaging  
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