Renal Cancer + Renal Cysts Flashcards

1
Q

What are the different types of renal cancer?

A

Renal cell carcinoma (adenocarcinoma) - 85%
Transitional cell
Nephroblastoma (Wilm’s tumour) - children
SCC - secondary to calculi, infection + schistosomiasis

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2
Q

How does RCC spread?

A
Direct invasion:
- perinephric tissues
- adrenal gland
- renal vein (tumour thrombosis)
Lymphatic:
- pre-aortic + hilar nodes
Haematological:
- bones
- liver
- brain
- lungs
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3
Q

What are the risk factors for RCC?

A
Smoking
Industrial exposure to carcinogens:
- cadmium, lead, aromatic hydrocarbons
Dialysis (30x increase)
Hypertension
Obesity
Anatomical abnormalities:
- polycystic kidneys
- horseshoe kidneys
Von Hippel-Lindau disease
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4
Q

What are the clinical features of RCC?

A
Haematuria (most common PC)
Flank pain
Flank mass
Lethargy, weight loss
Left mass --> left varicocele (compression left testicular vein)
Paraneoplastic syndrome
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5
Q

What paraneoplastic syndrome may be caused by RCC?

A

Epo –> polycythaemia
Parathyroid hormone –> hypercalcaemia
Renin –> hypertension
Pyrexia of unknown origin

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6
Q

Which investigations should be done for suspected RCC?

A

Routine bloods
Urinalysis (blood) + send for cytology
Initially USS or CT as for any haematuria

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7
Q

What is the gold standard for diagnosis of RCC?

A

CT abdo pelvis - pre and post IV contrast

Additional chest CT once diagnosis confirmed

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8
Q

How is RCC staged?

A
Stage 1:
- < 7cm and confined to renal capsule
Stage 2:
- > 7cm or invading renal capsule (but confined to Gerota's fascia)
Stage 3:
- extending into renal vein, vena cava or spread to 1 lymph node
Stage 4:
- beyond Gerota's fascia
- >1 local lymph node
- adrenal gland or perinephric fat
- distant mets
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9
Q

How is localised RCC managed?

A

Surgery:

  • partial nephrectomy
  • or radical nephrectomy

If not fit for surgery:

  • percutaneous radio frequency ablation
  • or cryotherapy
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10
Q

How is metastatic RCC managed?

A

Nephrectomy + immunotherapy (IFN alpha or IL-2 agents)

Chemo not effective for RCC

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11
Q

How are renal cysts classified?

A

Simple (well defined, homogenous)

Complex (thick walls, septations, calcification, heterogenous enhancement) –> risk of malignancy

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12
Q

Which genetic conditions cause renal cysts?

A

Polycystic kidney disease
Tuberous sclerosis
Von Hippel-Lindau disease

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13
Q

What are the types and features of polycystic kidney disease (PKD)?

A

Autosomal dominant PKD:
- mutations in PKD1 or PKD2 –> multiple renal cysts

Autosomal recessive PKD –> diagnosed in utero, most don’t survive first month of life

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14
Q

What are the clinical features of autosomal dominant PKD?

A

Associated with:

  • berry aneurysms
  • mitral valve disease
  • liver cysts

May present with uncontrolled hypertension or a flank mass

Patients eventually develop end stage renal failure –> dialysis or transplant

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15
Q

What are the clinical features of renal cysts?

A

Usually asymptomatic - found incidentally on imaging

Flank pain if cyst ruptures or becomes infected
Haematuria

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16
Q

Which investigations should be done for a suspected renal cyst?

A

Usually picked up on USS

But definitive diagnosis
–> CT or MRI with pre- and post- IV contrast images

17
Q

Which system is used to classify renal cysts and guide management?

A

Bosniak Scoring system
based on CT scan
- stage 1 is simple cyst
- stage 2-4 are complex

18
Q

What is the management of each stage of renal cyst?

A
1 --> no follow up
2 --> no follow up
2F --> CT at 3, 6 + 12 months
3 --> surveillance or surgical
4 --> surgical
19
Q

How can a symptomatic simple cyst be managed?

A

Simple analgesia initially
If significantly impacting patient:
- needle aspiration or cyst deroofing