Urothelial carcinoma of renal pelvis
Urothelial carcinoma of renal pelvis
Updated: 10/27/2022
© Jun Wang, MD, PhD
General features
- Commonly multifocal, probably through drop metastases
- May coexist with lower urinary tract urothelial carcinoma
- More common in male, mean age 67
- Likely non-invasive if low grade
Risk factors
- Tobacco use
- Phenacetin
- Industrial carcinogen exposure (coal, asphalt, petrochemicals, tar)
- Thorium containing radiologic contrast material
- Balkan endemic nephropathy
Clinical features
- Hematuria
- Flank pain
Pathological features
- Exophytic mass
- Papillary architecture lined by atypical urothelial cells
- Nests, clusters and single neoplastic cells with urothelial differentiation
Markers
- Positive for p63, uroplakin, CK7, CK20, PAX8
Genetic abnormality
- Microsatellite instability
- Complex karyotype if high grade
Diagnosis
- Radiologic studies
- Ureteropyeloscopy with cystoscopy
- Biopsy
- Urine cytology with molecular technologies such as FISH (Urovysion): only for high grade
Treatment
- Surgery
- Chemotherapy
Poor prognostic indicator
- High stage
- High tumor grade
- Vascular invasion
- Older age, metastasis
- Extensive tumor necrosis
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