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The genomic and epigenomic evolutionary history of papillary renal cell carcinomas [PDF]

open access: yesNature Communications, 2020
Many tumours are heterogenous, which calls into question whether multiple biopsies are required to accurately assess the cancer. Here, the authors show that papillary renal cell carcinoma is clonal in nature, suggesting that in this cancer one biopsy is ...
Bin Zhu   +25 more
doaj   +3 more sources

Clear cell and papillary renal cell carcinomas in hereditary papillary renal cell carcinoma (HPRCC) syndrome: a case report [PDF]

open access: yesDiagnostic Pathology, 2021
Background Hereditary papillary renal cell carcinoma (HPRCC) is a rare autosomal dominant disease characterized by the development of multiple and bilateral papillary type I renal cell carcinomas (RCC) and papillary adenomas caused by activating ...
Sophie Ferlicot   +6 more
doaj   +2 more sources

Bilateral Native Kidney Papillary Renal Cell Carcinomas in a 11-Year-Old Renal Transplant Patient [PDF]

open access: yesEuropean Journal of Pediatric Surgery Reports, 2022
Renal cell carcinomas (RCCs) are the most common renal tumors in adults and are usually sporadic and unilateral. Renal transplant recipients have an increased risk of developing RCC. RCC development after kidney transplantation is very rarely reported in
Çiğdem Ulukaya Durakbaşa   +7 more
doaj   +2 more sources

Primary Renal Carcinoid with Bilateral Multiple Clear Cell Papillary Renal Cell Carcinomas [PDF]

open access: yesCase Reports in Pathology, 2017
Clear cell papillary renal cell carcinoma (CCPRCC) is a newly recognized entity in the 2016 WHO classification and usually presents as a small, circumscribed, solitary mass of indolent nature.
Daniel A. Anderson, Maria S. Tretiakova
doaj   +2 more sources

Papillary renal cell carcinoma with malakoplakia: A unique case

open access: goldHuman Pathology Reports, 2022
The reported cases of malakoplakia concurrent with renal cell carcinoma (RCC) are exceedingly rare. Two prior cases of malakoplakia have been previously reported in patients with clear cell renal cell carcinoma.
Abigail A. Roth   +4 more
doaj   +2 more sources

Long-term response to nivolumab and acute renal failure in a patient with metastatic papillary renal-cell carcinoma and a PD-L1 tumor expression increased with sunitinib therapy: A case report.

open access: yesFrontiers in Oncology, 2016
Introduction: Papillary renal-cell carcinoma, which represents around 20% of renal cell carcinomas, is a heterogeneous disease that includes different tumor types with several clinical and molecular phenotypes.
Juan Ruiz-Bañobre   +5 more
doaj   +2 more sources

A distinct expression pattern and point mutation of c-kit in papillary renal cell carcinomas [PDF]

open access: bronzeModern Pathology, 2004
Zhen-Hua Lin   +6 more
semanticscholar   +3 more sources

Expression of Snail, Insulin-like mRNA-binding Protein3 and Aldehyde Dehydrogenase 1 as Diagnostic Markers in Clear Cell, Papillary, and Chromophobe Variants of Renal Cell Carcinoma [PDF]

open access: yesMiddle East Journal of Cancer, 2022
Background: Renal cell carcinoma (RCC) is the most prevalent malignancy of kidney. Snail is a zinc-finger transcription factor, associated with advanced tumor stage and poor prognosis of RCC.
Hanaa Atwa, Noha Elaidy
doaj   +1 more source

Clear Cell Papillary Renal Cell Carcinoma [PDF]

open access: yesArchives of Pathology & Laboratory Medicine, 2019
Clear cell papillary renal cell carcinoma (ccpRCC) is a recently recognized entity and represents the fourth most common variant of renal cell carcinoma (RCC). It has unique morphologic and immunohistochemical features and demonstrates an indolent clinical behavior.
Jianping, Zhao, Eduardo, Eyzaguirre
openaire   +3 more sources

A case of ipsilateral three simultaneous renal cell carcinomas with different histologic types

open access: yesIJU Case Reports, 2023
Introduction Few reports have presented sporadic multifocal renal cell carcinomas of different histologic types occurring simultaneously in a single kidney.
Satoki Tanaka   +9 more
doaj   +1 more source

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