Renal cell carcinoma associated with Xp11.2 translocation/transcription factor E3 gene fusion: an adult case report and literature review

Renal cell carcinoma (RCC) associated with Xp11.2 translocation/transcription factor E3 (TFE3) 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 Xp...

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Autores principales: Wang, Yuxiong, Wang, Yuantao, Feng, Mingliang, Lian, Xin, Lei, Yongsheng, Zhou, Honglan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545772/
https://www.ncbi.nlm.nih.gov/pubmed/33026261
http://dx.doi.org/10.1177/0300060520942095
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author Wang, Yuxiong
Wang, Yuantao
Feng, Mingliang
Lian, Xin
Lei, Yongsheng
Zhou, Honglan
author_facet Wang, Yuxiong
Wang, Yuantao
Feng, Mingliang
Lian, Xin
Lei, Yongsheng
Zhou, Honglan
author_sort Wang, Yuxiong
collection PubMed
description Renal cell carcinoma (RCC) associated with Xp11.2 translocation/transcription factor E3 (TFE3) 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.
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spelling pubmed-75457722020-10-20 Renal cell carcinoma associated with Xp11.2 translocation/transcription factor E3 gene fusion: an adult case report and literature review Wang, Yuxiong Wang, Yuantao Feng, Mingliang Lian, Xin Lei, Yongsheng Zhou, Honglan J Int Med Res Case Report Renal cell carcinoma (RCC) associated with Xp11.2 translocation/transcription factor E3 (TFE3) 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. SAGE Publications 2020-10-07 /pmc/articles/PMC7545772/ /pubmed/33026261 http://dx.doi.org/10.1177/0300060520942095 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Wang, Yuxiong
Wang, Yuantao
Feng, Mingliang
Lian, Xin
Lei, Yongsheng
Zhou, Honglan
Renal cell carcinoma associated with Xp11.2 translocation/transcription factor E3 gene fusion: an adult case report and literature review
title Renal cell carcinoma associated with Xp11.2 translocation/transcription factor E3 gene fusion: an adult case report and literature review
title_full Renal cell carcinoma associated with Xp11.2 translocation/transcription factor E3 gene fusion: an adult case report and literature review
title_fullStr Renal cell carcinoma associated with Xp11.2 translocation/transcription factor E3 gene fusion: an adult case report and literature review
title_full_unstemmed Renal cell carcinoma associated with Xp11.2 translocation/transcription factor E3 gene fusion: an adult case report and literature review
title_short Renal cell carcinoma associated with Xp11.2 translocation/transcription factor E3 gene fusion: an adult case report and literature review
title_sort renal cell carcinoma associated with xp11.2 translocation/transcription factor e3 gene fusion: an adult case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545772/
https://www.ncbi.nlm.nih.gov/pubmed/33026261
http://dx.doi.org/10.1177/0300060520942095
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