FAQ

Renal Angiomyoadenomatous Tumor

A very rare, benign, encapsulated tumor that arises from the kidney. It is characterized by the presence of clear epithelial cells in a prominent… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

2009-2015
01220092015

Related topics

Related topics

5 relations
KidneyKidney and UreterNeoplastic CellUrinary system
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Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Renal Angiomyoadenomatous Tumor
cancer cell
Kidney
Urinary system
Neoplastic Cell
Kidney and Ureter

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
Clear cell papillary renal cell carcinoma, renal angiomyoadenomatous tumor, and renal cell carcinoma with leiomyomatous stroma relationship of 3 types of renal tumors: a review.
Renal angiomyoadenomatous tumor has been described in 2000, followed by description of clear cell papillary renal cell carcinoma… (More)
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2015
2015
Clear cell papillary renal cell carcinoma and renal angiomyoadenomatous tumor: two variants of a morphologic, immunohistochemical, and genetic distinct entity of renal cell carcinoma.
Clear cell papillary renal cell carcinoma (ccpRCC) and renal angiomyoadenomatous tumor (RAT) share morphologic similarities with… (More)
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2011
2011
Clear cell renal cell carcinoma with focal renal angiomyoadenomatous tumor-like area.
Recently, renal angiomyoadenomatous tumor (RAT) has been identified. However, there are no descriptions about clear cell renal… (More)
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2011
2011
Low-grade renal carcinoma with histologic features overlapping with renal angiomyoadenomatous tumor and featuring polysomy 7 and 17 and a mutation in the von Hippel-Lindau gene: report of a hybrid…
To the Editor: It is with great interest that we read the recent articles by Kuroda et al [1,2]: “Clear cell renal carcinoma with… (More)
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2009
2009
Renal angiomyoadenomatous tumor: fluorescence in situ hybridization.
To the Editor: Renal angiomyoadenomatous tumor (RAT) is a very rare tumor and it was first described by Michal et al. 1 This… (More)
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