Renal Tumors Flashcards

1
Q

List extrarenal changes in CRF

A

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.

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2
Q

Describe G&M features of oncocytoma

A

G: well circumscribes large, brown mass with central stellate scar
M: formed of eosinophilic epithelial cells with uniform rounded nuclei

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3
Q

Age of incidence of RCC is……

A

60-70 yrs

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4
Q

Mention non-genetic risk factors for RCC

A

Smoking & with occupational exposure to cadmium
The risk is inc 30-fold in individuals with PKD due to chronic dialysis

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5
Q

Describe genetic predisposition to RCC

A
  1. Clear RCC; mostly sporadic maybe familial associated with VHL disease (tumor suppressor gene) leads to hemangioblastomas of cerebellum & retina & bilateral multiple clear cell carcinomas
  2. Papillary RCC aporadic or familial associated with MET proto-oncogene
  3. Chromophobe RCC; having multiple losses of entire chromosomes
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6
Q

RCC extends early into……& late into……

A

Renal pelvis
Renal capsule

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7
Q

The most common microscopic variant of RCC is…..while least common is…..

A

Clear
Chromphobe

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8
Q

GR: Presence of clear cells in RCC

A

Due to glycogen production

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9
Q

Describe spread of RCC

A

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

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10
Q

Describe microscopic features of Wilm’s tumor

A

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

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11
Q

Describe spread of Wilm’s tumor

A

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%)

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12
Q

List paraneoplastic syndromes accompanying RCC

A

Polycythemia, HTN, gynecomastia, hypercalcemia

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