Renal cell carcinoma (RCC) is a common and lethal urologic cancer, accounting for 2-3% of all adult malignancies. RCC most often occurs in the sixth and seventh decades of life and is more common in males. While most RCCs are sporadic, 2-3% are familial. Historically, clear cell and papillary RCC were thought to arise from the proximal convoluted tubules, while chromophobe and collecting duct RCC arise from more distal regions. RCCs are often circumscribed by compressed parenchyma rather than a true capsule. Prognostic tools combining multiple factors have improved predictions for patient outcomes. Approximately one-third of RCC patients present with