TFE3重排肾细胞癌的病例报告:摄取FDG-PET可能有助于诊断。

IF 1.9 Q3 ONCOLOGY
Journal of Kidney Cancer and VHL Pub Date : 2023-09-27 eCollection Date: 2023-01-01 DOI:10.15586/jkcvhl.v10i3.266
Sho Murakami, Keita Nagawa, Takanori Inui, Aya Yamamoto, Mizuka Suzuki, Fumitaka Koga, Toru Motoi, Yasunobu Takaki
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引用次数: 0

摘要

易位和转录因子E3(TFE3)-重排肾细胞癌(RCC)是一种罕见的RCCs亚型,其特征是染色体Xp11.2上的TFE3转录因子基因与多个基因之一融合。TFE3重排RCC主要发生在儿童和青少年,尽管也观察到中年病例。由于TFE3重排RCC的计算机断层扫描(CT)/磁共振成像(MRI)结果与其他RCC的结果重叠,鉴别诊断往往具有挑战性。在目前的病例报告中,我们强调了TFE3重排RCCs中氟-18标记的氟脱氧葡萄糖正电子发射断层扫描(FDG PET-CT)的特征。由于该疾病的罕见性,TFE3重排RCC的FDG PET-CT特征尚未报道。在我们的病例中,FDG PET-CT显示原发性肿瘤的高标准化摄取值(SUVmax)分别为7.14和6.25。这可能意味着TFE3重排的RCC具有很高的恶性潜能。当从葡萄糖代谢的角度考虑疾病的分子背景时,这是可以想象的。我们的病例表明,原发性肿瘤的高SUVmax是TFE3重排RCCs的临床特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Case Reports of TFE3-Rearranged Renal Cell Carcinoma: FDG-PET Uptake Might Help Diagnosis.

Case Reports of TFE3-Rearranged Renal Cell Carcinoma: FDG-PET Uptake Might Help Diagnosis.

Case Reports of TFE3-Rearranged Renal Cell Carcinoma: FDG-PET Uptake Might Help Diagnosis.

Case Reports of TFE3-Rearranged Renal Cell Carcinoma: FDG-PET Uptake Might Help Diagnosis.

Translocation and transcription factor E3 (TFE3)-rearranged renal cell carcinoma (RCC) is a rare subtype of RCCs characterised by the fusion of the TFE3 transcription factor genes on chromosome Xp11.2 with one of the multiple genes. TFE3-rearranged RCC occurs mainly in children and adolescents, although middle-aged cases are also observed. As computed tomography (CT)/magnetic resonance imaging (MRI) findings of TFE3-rearranged RCC overlap with those of other RCCs, differential diagnosis is often challenging. In the present case reports, we highlighted the features of the fluorine-18-labelled fluorodeoxyglucose positron emission tomography with CT (FDG PET-CT) in TFE3-rearranged RCCs. Due to the rarity of the disease, FDG PET-CT features of TFE3-rearranged RCC have not yet been reported. In our cases, FDG PET-CT showed high standardised uptake values (SUVmax) of 7.14 and 6.25 for primary tumours. This might imply that TFE3-rearranged RCC has high malignant potential. This is conceivable when the molecular background of the disease is considered in terms of glucose metabolism. Our cases suggest that a high SUVmax of the primary tumour is a clinical characteristic of TFE3-rearranged RCCs.

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