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Review of TFEB-amplified renal cell carcinoma with focus on clinical and pathobiological aspects
N. Kuroda, E. Sugawara, C. Ohe, F. Kojima, R. Ohashi, S. Mikami, Y. Nagashima, K. Peckova, M. Michal, O. Hes
Jazyk angličtina Země Polsko
Typ dokumentu časopisecké články, přehledy
NLK
Directory of Open Access Journals
od 2009
ProQuest Central
od 2009-01-01 do 2022-01-31
Open Access Digital Library
od 2009-01-01
Medline Complete (EBSCOhost)
od 2013-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2009
PubMed
35048631
DOI
10.5114/pjp.2021.111769
Knihovny.cz E-zdroje
- MeSH
- dospělí MeSH
- hybridizace in situ fluorescenční MeSH
- karcinom z renálních buněk * genetika MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádorové biomarkery genetika MeSH
- nádory ledvin * genetika MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- transkripční faktory BHLH-Zip genetika MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
The disease entity of TFEB-amplified renal cell carcinoma (RCC) has been recently established. In this article, we review such cases. Clinically, the age of patients ranged from 28 to 83 years with a mean age of 62.8 years. The size of the tumor ranged from 1.9 to 19.5 cm with a mean size of 8.7 cm. The tumor demonstrated a variety of architectural patterns such as solid, alveolar, papillary, pseudopapillary, nested or tubular. The International Society of Urological Pathology (ISUP) grade usually corresponds to grade 3 or 4. Cytomorphology shows eosinophilic, clear, amphophilic or even oncocytic cytoplasm. Necrosis can be frequently observed. Neoplastic cells with TFEB-amplified RCC show diffuse or patchy positivity for TFEB. Fluorescence in situ hybridization frequently show the amplification of more than 10 or 20 copies of the TFEB gene. Most TFEB-amplified RCCs behave in an aggressive fashion. Metastasis frequently occurs. In conclusion, this tumor seems to be characterized by occurrence in older patients, frequent necrosis, papillary/pseudopapillary growth pattern, high-grade nuclear grade, TFEB gene amplification, and aggressive clinical behavior. In order to clarify whether this tumor is a distinct entity from previously described renal tumors or not, a further examination in a large scale study will be required in the future.
Department of Diagnostic Pathology Keio University School of Medicine Tokyo Japan
Department of Diagnostic Pathology Kobe Kyodo Hospital Kobe Japan
Department of Human Pathology Wakayama Medical University Wakayama Japan
Department of Pathology and Laboratory Medicine Kansai Medical University Hirakata Japan
Department of Pathology Charles University Prague Faculty of Medicine in Plzen Pilsen Czech Republic
Department of Pathology The Cancer Institute Japanese Foundation for Cancer Research Tokyo Japan
Department of Surgical Pathology Tokyo Women's Medical University Tokyo Japan
Histopathology Core Facility Niigata University Faculty of Medicine Niigata Japan
Citace poskytuje Crossref.org
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- $a The disease entity of TFEB-amplified renal cell carcinoma (RCC) has been recently established. In this article, we review such cases. Clinically, the age of patients ranged from 28 to 83 years with a mean age of 62.8 years. The size of the tumor ranged from 1.9 to 19.5 cm with a mean size of 8.7 cm. The tumor demonstrated a variety of architectural patterns such as solid, alveolar, papillary, pseudopapillary, nested or tubular. The International Society of Urological Pathology (ISUP) grade usually corresponds to grade 3 or 4. Cytomorphology shows eosinophilic, clear, amphophilic or even oncocytic cytoplasm. Necrosis can be frequently observed. Neoplastic cells with TFEB-amplified RCC show diffuse or patchy positivity for TFEB. Fluorescence in situ hybridization frequently show the amplification of more than 10 or 20 copies of the TFEB gene. Most TFEB-amplified RCCs behave in an aggressive fashion. Metastasis frequently occurs. In conclusion, this tumor seems to be characterized by occurrence in older patients, frequent necrosis, papillary/pseudopapillary growth pattern, high-grade nuclear grade, TFEB gene amplification, and aggressive clinical behavior. In order to clarify whether this tumor is a distinct entity from previously described renal tumors or not, a further examination in a large scale study will be required in the future.
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