Tumors of the Kidney
TUMORS OF THE KIDNEY
Benign tumours of the kidney are as follows:
- Cortical adenomas are small, encapsulated cortical nodules measuring <3 cm; they are a common finding at autopsy. They may be composed of tubular or papillary structures. The papillary adenomas share the same chromosomal gains as papillary renal cell carcinoma.
- Angiomyolipomas are hamartomas composed of fat, smooth muscle, andblood vessels, common in patients with tuberous sclerosis.
- Oncocytomas are large, benign tumours that are resected to rule out renal cellcarcinoma when they are found incidentally on imaging studies. They are brown on cut surface and have abundant pink cytoplasm on microscopy.
Renal cell carcinoma (RCC) is the most common age 50–70, with males affected more than females.
Risk factors include cigarette smoking, chronic analgesic use, asbestos exposure, chronic renal failure, acquired cystic disease, and von Hippel-Lindau disease (VHL tumour suppressor gene).
In 10% of cases, the “classic” triad occurs:
- Palpable mass
- Flank pain
A variety of paraneoplastic syndromes from ectopic hormone production can occur:
- Polycythemia (erythropoietin production)
- Hypertension (renin production)
- Cushing syndrome (corticosteroid synthesis)
- Hypercalcemia (PTH-like hormone)
- Feminization of masculinization (gonadotropin release)
Renal cell carcinoma may also cause secondary amyloidosis, a leukemoid reaction, or eosinophilia.
There is a high incidence of metastasis on initial presentation. The clinical course is unpredictable.
Gross examination typically demonstrates a large, solitary yellow mass found most commonly in the upper pole. Areas of necrosis and haemorrhage are commonly present. The tumour often invades the renal vein and may extend into the inferior vena cava and heart.
Histologic types of RCC are as follows:
Clear cell RCC (most common)
- Often invades renal venous system
- May have loss of genetic material in 3p
- A small per cent occur in association with von Hippel-Lindau disease
- Microscopically, there is an alveolar growth pattern with microcysts
- Tumor is resistant to chemotherapy and radiotherapy
- Tends to be bilateral and multifocal
- The cut surface is granular
- Microscopically, the papillae have a single layer of cells
- Gains of chromosome 7 and 17 are common
- Duplications of chromosome 7 increase dosage of protooncogene MET
Chromophobe RCC (rare)
- Have cells that stain more darkly than clear cell RCC
- Have loss of multiple chromosomes
- Least aggressive of the RCCs
Wilms tumour (nephroblastoma) typically presents age 2-5 as a large abdominal mass.
Patients with WAGR, DDS, or BWS syndrome are at increased risk of Wilms tumour.
- WAGR syndrome is the cluster of Wilms tumour, aniridia, genital anomalies, and mental retardation.
- Beckwith-Wiedemann syndrome (BWS) is an overgrowth disorder with char-act eristic features and an attendant increased risk of cancer.
- Denys-Drash syndrome (DDS) affects the genitalia and kidneys.
Both WAGR and DDS are associated with deletions and mutations, respectively, of the WT1 gene. BWS arises through imprinting abnormalities at the WT2 locus.
Pathologically, Wilms tumour causes a large, solitary tan mass. Microscopic examination reveals a tumour containing 3 elements: metanephric blastema, epithelial elements (immature glomeruli and tubules), and stroma.
Treatment is surgery, chemotherapy, and radiation, which as a combined therapy yields an excellent prognosis. The long-term survival rate is 90%.
Transitional cell carcinomas can involve the renal pelvis as well as the urinary bladder.