FN: Renal Tumours Flashcards

1
Q

Renal cell carcinoma/Hypernephroma epi

A

90$ of renal cancers
Age: 55 yrs
Sex: M>F =2:1

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2
Q

Renal cell carcinoma/Hypernephroma RF

A
Obesity
Smoking
HTN
Dialysis (15% of pts. develop RCC)
4% heritable e.g. VHL syndrome
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3
Q

Renal cell carcinoma/Hypernephroma pathology

A

Adenocarcinoma from proximal renal tubular epithelium

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4
Q

Renal cell carcinoma/Hypernephroma subtypes

A

Clear cell (glycogen):70-80%
Papillary: 15%
Chromophobe:5%
Collecting duct:1%

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5
Q

Renal cell carcinoma/Hypernephroma PResentation

A

50% incidental finding
Systemic: anorexia, malaise, wt. loss, PUO
Clot retention
Invasion of L renal vein - varicocel (1%)
Cannonball mets - SOB

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6
Q

Renal cell carcinoma/Hypernephroma Triad

A

HAematuria
Loin pain
loin mass

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7
Q

Renal cell carcinoma/Hypernephroma Paraneoplastic features

A
EPO - polycythaemia
PTHrP - raised Calcium
Renin - HTN
ACTH - Cushings syn
Amyoidosis
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8
Q

Renal cell carcinoma/Hypernephroma spread

A

Direct: renal vein
Lymph
Haematogenous: bone, liver and lung

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9
Q

Renal cell carcinoma/Hypernephroma Investigations blood shows

A

Polycythaemia, ESRm U+E, ALP, Ca

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10
Q

Renal cell carcinoma/Hypernephroma Urine

A

Dip

Cytology

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11
Q

Renal cell carcinoma/Hypernephroma Imaging

A

CXR: cannonballmets
US: mass
IVU: filling defect
CT/MRI

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12
Q

Renal cell carcinoma/Hypernephroma Robson staging

A
  1. Confined to kidney
  2. Involves perinephric fat, but not Garotas fascia
  3. Involves perinephric fat, but not Garotas fascia
  4. Spread into renal vein
  5. Spread to adjacent/distant organs
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13
Q

Renal cell carcinoma/Hypernephroma Medical Mx

A

REserved for pts. with poor prognosis

Temsirolimus (mTOP inhibitor)

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14
Q

Renal cell carcinoma/Hypernephroma Mx surgical

A

Radical nephrectomy

Consider partial if small tumour of 1 kidney

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15
Q

Transitional cell Carcinoma Epi

A

2nd commonest renal cancer
Age: 50-55yrs
Sex: M>F=4:1

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16
Q

Transitional cell Carcinoma RF

A

Smoking
Amine exposure (rubber industry)
Cyclophosphamide

17
Q

Transitional cell Carcinoma Pathology

A
Hihgly malignant
Locations
-bladder 50%
Ureter
REnal pelvis
18
Q

Transitional cell Carcinoma Presentation

A

Painless haematuria
Freqeuncy, urgency, dysuria
Urinary tract obstruction

19
Q

Transitional cell Carcinoma Investigations

A

Urine cytology
CT/MRI
IVU: pelvicael filing defect

20
Q

Transitional cell Carcinoma MA

A

Nephrouretctomy

REgular f/up: 50% develop bladder tumours

21
Q

Nephroblastoma: Wilms tumour

A

Childhood tuour of primitve renal tubules and mesenchymal cells
May be association with Chr 11 mutation
May be association with WAGR syndrome - wilms, aniridia, GU abnormalities, REtardation

22
Q

Nephroblastoma: Wilms tumour Presentation

A
2-5 yrs
5-10% bilateral
Abdo mass (doesnt cross the midline)
Haematuria
Abdo pain
GTN
23
Q

Benign neoplasms

A

Cysts: very common
Renal papillary adenomas
Oncocytoma: eosinophilic cells with numerous mitochondria
Angiomyolipoma: seen in tuberous sclerosis

24
Q

Malignant neoplasms

A

SCC: associations with chronic infected staghom calculi

25
Q

Benign tumours note

A

Commonly require nephrectomy to exclude malignancy