Renal Tumors Flashcards
List extrarenal changes in CRF
Fibrinous pericarditis & pleurisy, uremic pneumonitis, enterocolitis & ulceration, immunodeficiency, osteodystrophy due to 2ry hyperparathyroidism, normocytic normochromic anemia due to dec erythropoietin, nervous manifestations (mental changes, peripheral neuritis & coma), fluid, electrolyte & acid-base imbalance.
Describe G&M features of oncocytoma
G: well circumscribes large, brown mass with central stellate scar
M: formed of eosinophilic epithelial cells with uniform rounded nuclei
Age of incidence of RCC is……
60-70 yrs
Mention non-genetic risk factors for RCC
Smoking & with occupational exposure to cadmium
The risk is inc 30-fold in individuals with PKD due to chronic dialysis
Describe genetic predisposition to RCC
- Clear RCC; mostly sporadic maybe familial associated with VHL disease (tumor suppressor gene) leads to hemangioblastomas of cerebellum & retina & bilateral multiple clear cell carcinomas
- Papillary RCC aporadic or familial associated with MET proto-oncogene
- Chromophobe RCC; having multiple losses of entire chromosomes
RCC extends early into……& late into……
Renal pelvis
Renal capsule
The most common microscopic variant of RCC is…..while least common is…..
Clear
Chromphobe
GR: Presence of clear cells in RCC
Due to glycogen production
Describe spread of RCC
Local infiltration
Blood spread due to renal vein invasion common sites are lung & bones (pelvis & femur), CNS, adrenals. Left renal vein invasion leads to variocele
Lyphatic spread to lumbar group of LNs
Describe microscopic features of Wilm’s tumor
3 components
1. Blastematous areas, extremely cellular composed of round to oval cells with scanty cytoplasm
2. Mesenchymal elements have spindle cell fibroblast-like configuration may show mesenchymal differentiation
3. Epithelial component; show glandular, tubular or glomerular formation
Describe spread of Wilm’s tumor
Local infiltration with destruction of kidney tissue, invasion of renal capsule, perirenal soft tissue, adrenal gland, bowel, liver or vertebra.
Blood spread; most common to LL & brain
Lymphatic spread to regional LNs (15%)
List paraneoplastic syndromes accompanying RCC
Polycythemia, HTN, gynecomastia, hypercalcemia