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TFEB-associated renal cell carcinoma: A case report and literature review
TFEB-associated renal cell carcinoma is very rare and belongs to the microphthalmia — associated transcription family translocation renal cell carcinoma. PATIENT CONCERNS: Hospitalized for fever, a 29-year-old male patient had a left kidney lesion without any additional discomfort. DIAGNOSES: Histop...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771232/ https://www.ncbi.nlm.nih.gov/pubmed/36550835 http://dx.doi.org/10.1097/MD.0000000000031870 |
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author | Zhu, Yong Xia, Chengxing Ou, Yitian Zhang, Chao Li, Lin Yang, Delin |
author_facet | Zhu, Yong Xia, Chengxing Ou, Yitian Zhang, Chao Li, Lin Yang, Delin |
author_sort | Zhu, Yong |
collection | PubMed |
description | TFEB-associated renal cell carcinoma is very rare and belongs to the microphthalmia — associated transcription family translocation renal cell carcinoma. PATIENT CONCERNS: Hospitalized for fever, a 29-year-old male patient had a left kidney lesion without any additional discomfort. DIAGNOSES: Histopathological and immunohistochemical results were corresponding with TFEB renall cell carcinoma features. INTERVENTIONS: Surgical resection of the tumor was performed. OUTCOMES: After 8 months of follow-up, no tumor recurrence was observed. LESSONS: TFEB-associated renal cell carcinoma is rare. The diagnosis is explicit. However, the optimal treatment needs to be further explored. |
format | Online Article Text |
id | pubmed-9771232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-97712322022-12-22 TFEB-associated renal cell carcinoma: A case report and literature review Zhu, Yong Xia, Chengxing Ou, Yitian Zhang, Chao Li, Lin Yang, Delin Medicine (Baltimore) 5700 TFEB-associated renal cell carcinoma is very rare and belongs to the microphthalmia — associated transcription family translocation renal cell carcinoma. PATIENT CONCERNS: Hospitalized for fever, a 29-year-old male patient had a left kidney lesion without any additional discomfort. DIAGNOSES: Histopathological and immunohistochemical results were corresponding with TFEB renall cell carcinoma features. INTERVENTIONS: Surgical resection of the tumor was performed. OUTCOMES: After 8 months of follow-up, no tumor recurrence was observed. LESSONS: TFEB-associated renal cell carcinoma is rare. The diagnosis is explicit. However, the optimal treatment needs to be further explored. Lippincott Williams & Wilkins 2022-12-16 /pmc/articles/PMC9771232/ /pubmed/36550835 http://dx.doi.org/10.1097/MD.0000000000031870 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | 5700 Zhu, Yong Xia, Chengxing Ou, Yitian Zhang, Chao Li, Lin Yang, Delin TFEB-associated renal cell carcinoma: A case report and literature review |
title | TFEB-associated renal cell carcinoma: A case report and literature review |
title_full | TFEB-associated renal cell carcinoma: A case report and literature review |
title_fullStr | TFEB-associated renal cell carcinoma: A case report and literature review |
title_full_unstemmed | TFEB-associated renal cell carcinoma: A case report and literature review |
title_short | TFEB-associated renal cell carcinoma: A case report and literature review |
title_sort | tfeb-associated renal cell carcinoma: a case report and literature review |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771232/ https://www.ncbi.nlm.nih.gov/pubmed/36550835 http://dx.doi.org/10.1097/MD.0000000000031870 |
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