Urology - Renal Tumours Flashcards

1
Q

What is most common renal tumour?

A
  • Renal cell carcinoma (80% of renal tumours) - arise from renal tubules)
  • Malignant tumours can be 1ry or 2ry but secondary tumours are rare (anatomy - higher up than rest of urology system)
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2
Q

RCC: epidemiology

A
  • 80-90% of renal tumours
  • age: 55ya
  • Sex: M>F = 2:1
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3
Q

RCC: risk factors

A
  • obesity
  • smoking
  • then
  • dialysis: 15% of pts develop RCC
  • 4% heritable
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4
Q

RCC: pathology

A
  • Adenocarcinomas from proximal renal tubular epithelium

- Subtypes: clear cell (70%), papillary (15%), chromophobe (5%) and collecting duct (1%)

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5
Q

RCC: Presentation

A
  • 50% of pts are discovered as incidental finding - have USS/CT for unrelated reason
  • Triad (rare): haematuria, loin pain and loin mass
  • Systemic: anorexia, malaise, wt loss
  • Clot retention
  • Invasion of left renal vein: varicocele (1%)
  • Cannonball mets: SOB
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6
Q

RCC: paraneoplastic features

A
  • EPO: polycythaemia
  • PTHrP: hypercalcaemia
  • Renin: HTN
  • ACTH: Cushing’s syndrome
  • Amyloidosis
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7
Q

RCC: potential avenues of spread

A
  • direct: renal vein (varicocele on LHS)
  • lymph
  • haematogenous: bone, liver and lung
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8
Q

Ix

A
  • Blood: FBC (check polycythaemia), ESR, U+E, ALP, Ca
  • Urine: dip and cytology
  • DRE!!
  • Imaging: CXR (cannonball mets), US (mass), IVU (filling defect), staging CT/MRI CAP
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9
Q

What is the name of staging system for RCC and outline the steps

A
  • Robson staging
    1. Confined to kidney
    2. Involves perinephric fat but not Garota’s fascia
    3. Spread into renal vein
    4. Spread to adjacent/distant organs
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10
Q

RCC: Mx - medical and surgical

A
  • *These cancers are very resistant to chemotherapy and radiotherapy - v rarely used
  • Medical: reserved for pts with poor prognosis
  • Surgical: radical nephrectomy or consider partial if pt only has 1 kidney, very poor kidney function or small tumour
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11
Q

TCC/Pelviureteric tumours: epidemiology and risk factors

A
  • 2nd most common renal cancer
  • Age: 50-80
  • Risk factors: smoking, amine exposure (rubber industry), cyclophosphamide
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12
Q

TCC/Pelviureteric tumours: pathology

A
  • same as TCC of bladder but account for less than 20% of renal tumours
  • highly malignant
  • location: bladder, ureter and pelvis
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13
Q

TCC/Pelviureteric tumours: presentation

A
  • Painless haematuria
  • frequency, urgency, dysuria
  • urinary tract obstruction
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14
Q

TCC/Pelviureteric tumours: Ix

A
  • Urine cytology
  • same bloods as RCC
  • CT/MRI (KUB or staging CAP)
  • IVU: look for filling defect
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15
Q

TCC/Pelviureteric tumours: Mx

A
  • Nephro-uretectomy

- need very regular follow up b/c 50% subsequently develop bladder tumours :(

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16
Q

Wilm’s tumour: what is it? When does it present? What mutations is it associated with?

A
  • Aggressive childhood tumour of primitive renal tubules and mesenchymal cells
  • May be associated with: Chr 11 mutation or WAGR syndrome
  • commonest intra-abdo tumour in <10ya, if caught early survival is high but can be rapid/aggressive and metastasise to lungs (Rx is radical nephrectomy and stage-dependant post-op Chemo)
17
Q

Wilm’s tumour: presentation

A
  • 2-5ya
  • 5-10% are bilateral
  • Abdo mass/pain
  • haematuria
  • HTN
  • Aggressive: mets to lungs?
18
Q

Other neoplasms: benign

A
  • Cysts are very common
  • Renal papillary adenomas
  • Oncocytoma: eosinophilic cells with numerous mitochondria
  • Angiomyolipoma: seen in tuberous sclerosis
  • *Bening tumours commonly require nephrectomy to exclude malignancy
19
Q

Other neoplasms: malignant

A

-SCC associated with infected staghorn calculus