Renal Neoplastic Disease Flashcards
Renal Cell Carcinoma Epidemiology
Male predominance: RCC is approximately 50% more common in men than women
Highest incidence between age 60-80
Renal Cell Carcinoma Risk factors
Smoking 1/3 of cases Hypertension Obesity Acquired cystic disease of the kidney Occupational Exposure Analgesics Genetic factors Chronic hepatitis C infection
Renal Cell Carcinoma Types : Clear cell carcinomas (75-85%)
arise from the proximal tubule
typically have a deletion of chromosome 3p
Macroscopically, they may be solid or less commonly cystic.
In addition to occurring in sporadic disease, associated with von Hippel-Lindau disease.
Renal Cell Carcinoma Types: Papillary (“chromophilic”) carcinoma (familial or sporadic) (10-15%)
Thought to arise from proximal convoluted tubule
Trisomy 7 common
Tends to be multifocal and bilateral
Recent study shows better prognosis than clear cell carcinoma
Renal Cell Carcinoma Types: Chromophobe renal cell carcinoma
Histologically, composed of sheets of cells that are darker than clear cell carcinoma
5-10% of renal cell carcinomas
Arise from intercalated cells of collecting ducts
lower risk of disease progression and death compared to clear cell carcinomas
Renal Cell Carcinoma Types: Collecting duct carcinoma (Bellini duct carcinoma)
Approximately 1% of renal cell carcinomas
Aggressive clinical course
Affects younger adults and black patients more frequently
Renal Cell Carcinoma Types: Oncocytomas (3-7%)
originate from the intercalated cells of the collecting ducts
consist of oncocytes, which are large well-differentiated neoplastic cells with intensely eosinophilic granular cytoplasm
Mutations in c-met oncogene associated with papillary RCC
Tends to be unilateral and single, but multiple and bilateral oncocytomas have been described
Renal Cell Carcinoma: Classic” triad (found in 9% only)
Hematuria (60%) Flank pain (40%) Palpable mass (45%)
3 Major Criteria for simple cyst
Mass is round and sharply demarcated with smooth walls
No echoes (anechoic) within the mass
Strong posterior wall echo indicating good transmission through the cyst
Wilms’ Tumor (Nephroblastoma)
Pediatric Tumor
The most common renal malignancy in children
Mean age 3.5 years
Caused by abnormal renal development in utero, or genetic mutation
Wilms’ Tumor: Clinical Features
Palpable mass in 90% of cases: May be large, extending into pelvis Abdominal pain in 30% Hematuria 12-25% Hypertension in 25% 5-10% bilateral
Benign Renal Tumors
Papillary adenoma
fibroma/hamartoma
Angiomyolipoma