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- W2025556592 abstract "Until recently, kidney cancer was thought to represent a single disease, presumably arising from a common renal cell progenitor. Clinicians and pathologists relied on histopathologic criteria, predominantly using hematoxylin-eosin staining, immunohistochemistry, and electron microscopy to diagnose renal cancers. It has become increasingly recognized that a variety of benign and malignant cancers arise from the kidney. Several new subtypes of renal cell carcinoma (RCC) have been described and refined in the past few decades, initially on the basis of cytologic features and architectural patterns and subsequently on the basis of cytogenetic and molecular biologic findings. The most recent classification scheme adopted by the American Joint Committee on Cancer and the Union International Contre le Cancer in 1997 classified benign tumors as papillary adenoma, metanephric adenoma, and renal oncocytoma and malignant cancers as clear cell carcinoma (conventional RCC), papillary carcinoma, chromophobe carcinoma, collecting duct carcinoma with medullary carcinoma of the kidney, and RCC unclassified. 1 Bostwick D.G. Eble J.N. Murphy G.P. Conference summary diagnosis and prognosis of renal cell carcinoma—1997 workshop. Cancer. 1997; 80: 975-976 Crossref Scopus (22) Google Scholar" @default.
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- W2025556592 date "2002-12-01" @default.
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- W2025556592 title "Molecular genetics and histopathologic features of adult distal nephron tumors" @default.
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