5-Minute Clinical Consult

Renal Cell Carcinoma

Renal Cell Carcinoma was found in 5-Minute Clinical Consult which helps you diagnose, treat, and follow up on over 900 medical conditions seen in everyday practice.

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Basics

Description

  • Renal cell carcinoma (RCC), (aka hypernephroma or Grawitz tumor), accounts for 3–4% of all adult cancers and 2.3% of all cancer deaths; 7th most common malignant tumor in men and 9th in women
  • Characterized by obscure and varied presentations, including paraneoplastic syndromes, vascular findings, and uncommon metastatic sites
  • Early, aggressive surgical management provides the best opportunity for cure.
  • System(s) affected: Renal/Urologic

Epidemiology


Incidence
  • Predominant age: Patients in 5th–7th decades; median age at diagnosis is 66 years.
  • Predominant sex: Male > Female (1.6:1)
  • Age-adjusted incidence increasing 3%/yr, likely due in part to increased detection as an incidental finding on imaging studies
  • In males, 10.7 new cases of RCC per 100,000 population per year vs. 6.5 in females
  • Between 1975 and 1998, incidence among African Americans increased by 4.5% compared with 2.9% among Caucasians; reasons are unclear.

Risk Factors

  • Smoking, active and passive (increases relative risk by 2–3)
  • Obesity (linear relationship in women)
  • Hypertension (antihypertensive medications are not independently associated with RCC)
  • End-stage renal failure
  • Acquired renal cystic disease
  • Tuberous sclerosis
  • HIV infection
  • Urban environment
  • Heavy metal exposure (cadmium, lead)
  • Environmental toxin exposure (asbestos, petroleum by-products, chlorinated solvents)
Genetics
  • 2–3% of cases are familial, with several autosomal-dominant syndromes described.
  • Oncogenes localized to the short arm of chromosome 3 may have etiologic implications. Chromosome 3p12–p26 is specific for clear cell RCC.
  • People with HLA types Bw44 and DR8 are prone to develop RCC. These are rare familial RCCs.
  • Hereditary papillary RCC is an autosomal-dominant form of disease associated with multifocal papillary renal tumors and a 5:1 male predominance.

General Prevention

Smoking may contribute to 1/3 of all cases.

Etiology

Unknown

Commonly Associated Conditions

  • Von Hippel–Lindau disease: 30–45% of these patients develop clear cell tumors.
  • Tuberous sclerosis: Associated primarily with angiomyolipoma and clear cell tumors
  • Sickle-cell trait: With few exceptions, renal medullary tumor is seen in young African American males with sickle-cell trait.
  • Adult polycystic kidney disease
  • Horseshoe kidney
  • Acquired renal cystic disease from chronic renal failure

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