renal tumours Flashcards

1
Q

What benign renal tumours exist? 6

A
Renal cyst
Oncocytoma
Angiomyolipoma
Fibroma
Adenoma
Juvenile granulosa cell tumour (JGCT)
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2
Q

Benign renal cyst:

  • What is this?
  • is it common?
  • what is cystic degeneration? treatment of this?
  • what are the clinical features?
  • how is this diagnosed?
A

=fluid filled space in kidney, solitary or multiple

Epidemiology: 1/10 people, 50% of those over 50yrs will have 1 or more, represent 70% of benign asymptomatic renal lesions

Cystic degeneration: this is where multiple cysts enlarge with time. Occurs regularly in end stage kidney disease. Treated with dialysis/transplantation

Clinical features of cyst: some may cause pain/haematuria if large

Diagnosis: USS (incidental finding), bleeding may occur within cyst, contrast CT may show if cysts have become complicated

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3
Q

Renal fibroma: what is this?

A

Common benign tumour, medullary in origin with white nodules

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4
Q

Renal adenoma: what is this?

A

Benign tumour, cortical in origin with yellowish nodules <2cm

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5
Q

Angiomyolipoma:

  • what is this?
  • what is it assoc. with?
  • what can this cause?
  • Imaging
  • When are these removed?
  • what other treatment is available?
A

= RARE tumour with mixture of fat, muscle and blood vessels (imitates RCC) assoc. with tuberose sclerosis

  • Blood vessels are very fragile and can cause haemorrhage (could be cause of wunderlich syndrome)
  • CT shows unmistakable appearance due to fat content
  • remove if larger than 6cm = high risk haemorrhage
  • can do embolisation
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6
Q

What do JGCT produce? what does this cause?

A

-produces renin

=secondary hypertension

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7
Q

Oncocytoma:

  • what is this?
  • what does this imitate?
  • diagnosis?
  • treatment
  • what is seen on CT
A

=benign tumour that imitates RCC, represents 3-7% renal masses

-imitates RCC as some areas of RCC can look like oncocytoma on biopsy

Diagnosis:

  • no definitive diagnosis except on nephrectomy which should be done as may be RCC or may grow
  • on CT there’s a central scar present due to central necrosis
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8
Q

What 3 malignant renal cell tumours exist?

A
  • Nephroblastoma (wilm’s tumour)
  • Urothelial carcinoma
  • Renal cell carcinoma
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9
Q

Wilm’s tumour - which patient’s does this affect? what three symptoms to look out for?

A

most common intrabdominal tumour in children

abdominal mass (most common presenting feature)
painless haematuria
flank pain

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10
Q

Urothelial carcinoma - where do these arise?

A

renal pelvis and calyces

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11
Q

Renal cell carcinoma:

  • what is this also known as?
  • what is the classic triad of presentation seen in 15%
  • how else can this present? 2
A

AKA clear cell Ca/hypernephroma/grawitz tumour

Triad of presentation:

  • loin pain 40%
  • renal mass 25%
  • Frank haematuria 60%

Other presentations:

  • incidental finding on imaging
  • it can cause paraneoplastic syndrome even if no met.s (weight loss/anaemia/hypercalcaemia)
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12
Q

RCC:

  • male or female preponderance?
  • common age affected
  • what is seen pathologically?
  • what syndrome is bilateral tumours seen in?
A

M:F 2:1

Age 65-75yo

pathology:
-adenoma of the proximal tubule - cells are clear cells of papillary type. can be multifocal or bilateral

Bilateral tumours seen in von hippel lindau

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13
Q

RCC:

  • what is standard treatment?
  • How to treat if renal function needs to be preserved or if tumour is only small or oncologically ‘safe’
  • what if the patient is not fit/multiple tumours/bilateral tumours
A

Standard treatment: radical nephrectomy usually done laparoscopically (tumour is not radiosensitive)

  • if want to preserve renal function or if tumour is only small or oncologically ‘safe’ can do partial nephrectomy (open surgery/larger surgery)
  • if pt. not fit/multiple tumours/bilateral tumours can do radiofrequency ablation or cryoablation
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14
Q

When doing surgery for RCC are the adrenal glands also removed?

A

-only remove if involved as risk of spread to either adrenal gland is equal

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15
Q

Describe the staging of renal cell carcinoma. Why does it tend to spread up the vena cava?

A

Stage 1 - tumour in capsule

Stage 2 - tumour invasion perinephric fat (confined by fascia)

Stage 3 - tumour involvement regional lymph nodes and or renal vein/vena cava

Stage 4 - adjacent organs/distant mets

-tends to spread up vena cava as the capsule of the kidney is thick

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16
Q

Describe adjuvant therapy options for RCC metastases

A

Sunitab - tyrosine kinase inhibitor, acts to inhibit VEGF/PDGF (reduces neovascularisation)

17
Q

What is the prognosis of RCC if no mets?

A

-5 yr survival 60-70%