Highlights & Basics
- Renal cell carcinoma (RCC) is a malignancy arising from the renal parenchyma/cortex. Clear cell RCC accounts for the majority (80% to 90%) of primary renal malignancies.
- Incidence is increasing along with stage migration to more early-stage diagnosis due to the frequent use of sensitive imaging. Often asymptomatic and diagnosed incidentally.
- Most cases are sporadic, although at least four hereditary clinical kidney cancer syndromes have been identified.
- Assessment of primary tumor, regional lymph nodes, distant metastasis, and classification of histologic subtypes are of paramount importance for making treatment decisions.
- Surgery for early/local disease can be curative in over 90% of patients; surveillance and/or biopsy may be the most appropriate strategy in some patients with small renal masses. Risk of distant relapse remains 30% for curatively resected RCC.
Quick Reference
History & Exam
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Definition
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Citations
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American College of Radiology. ACR appropriateness criteria: post-treatment follow-up and active surveillance of clinically localized renal cell carcinoma. 2021 [internet publication].[Full Text]
Rathmell WK, Rumble RB, Van Veldhuizen PJ, et al. Management of metastatic clear cell renal cell carcinoma: ASCO guideline. J Clin Oncol. 2022 Sep 1;40(25):2957-95.[Abstract][Full Text]
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