Renal Cancer Flashcards

1
Q

What treatment are renal cancers resistant to?

A

Chemotherapy
Radiotherapy

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2
Q

How is metastatic disease managed?

A

Biological therapy

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3
Q

Which cancers are managed with partia nephrectomy?

A

T1 tumours
Below 4cm

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4
Q

Which cancers are managed with radical nerve to my?

A

T2 tumours
Above 4cm mass

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5
Q

What are the types of renal tumours?

A

Renal carcinoma

Transitional cell carcinoma

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6
Q

What is renal cell carcinoma?

A

Renal cell carcinoma (RCC) is an adenocarcinoma of the renal cortex that originates from proximal convoluted tubules. Macroscopically, these tumours are well circumscribed, with a yellowish appearance denoting their high fat and glycogen content.

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7
Q

What is a transitional cell carcinoma?

A

Transitional cell carcinoma (TCC) of the renal pelvis is a carcinoma type that shares properties with TCC of the bladder and ureter. Macroscopically, these lesions can be papillary or flat (sessile), and microscopically, TCC shows areas of squamous differentiation, extensive keratinization and intracellular bridges.

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8
Q

What are the risk factors for renal cel caricnoma?

A

European
North American ethnicity
Obesity
Smoking
Low vitamin diet
Hypertensions

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9
Q

What are the paraneoplastic syndrome with renal carcinoma?

A

High EPO production causing ruddy complexion
PTHrp secretion causing hypercalcaemia
ACTH secretion causing Cushing’s disease

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10
Q

What is the referral criteria for rneal carcinoma?

A

they are aged 45 years and over and have:
Unexplained visible haematuria without urinary tract infection, or
Visible haematuria that persists or recurs after successful treatment of urinary tract infection

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11
Q

What imaging assesses for metastatic disease?

A

CT chest and abdomen

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12
Q

When is chemotherapy offered?

A

Patients with Nicolette resection tor deuce recurrence chances

Palliative patients

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13
Q

When is radiotherapy offered?

A

Palliative care

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14
Q

What is the most common rena malignancy in children?

A

Wilm’s tumour between the ages of 2 and 5

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15
Q

What cancer is associated with sickle cell trait?

A

Renal medullary carcinoma which predominately affect the right side of the

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16
Q

What is the diagnostic imaging for renal cancer?

A

USS abdomen and renal tract to assess for renal pelvis too

17
Q

Which imaging assess lower urinary tract?

A

CT urogram and cystoscopy

18
Q

What is a risk in renal cancer in regard to surrounding structures?

A

Obstruction of IVC causing bilateral pedal oedema

19
Q

What is Stauffer syndrome?

A

a paraneoplastic disorder associated with renal cell cancer
typically presents as cholestasis/hepatosplenomegaly
it is thought to be secondary to increased levels of IL

20
Q

What is Von Hippel Laundau syndrome?

A

characterized by hemangioblastomas of the brain, spinal cord, and retina; renal cysts and clear cell renal cell carcinoma

21
Q

What reduces tumour size?

A

alpha-interferon and interleukin-2 have been used to reduce tumour size and also treat patients with metatases

22
Q

What is nephroblastoma commonly known as?

A

Wilm’s tumours

Nephroblastoma is a type of kidney cancer that primarily affects children.

23
Q

At what age does nephroblastoma usually present?

A

In the first 4 years of life

Most cases are diagnosed in children under 5 years old.

24
Q

What are common symptoms of nephroblastoma?

A

A mass associated with haematuria and pyrexia may occur in 50%

Haematuria refers to the presence of blood in urine.

25
Where do nephroblastoma metastases typically occur?
Usually to the lung ## Footnote Early metastasis to the lungs is a common characteristic of nephroblastoma.
26
What is the primary treatment for nephroblastoma?
Nephrectomy ## Footnote Nephrectomy is the surgical removal of the kidney.
27
What is the prognosis for younger children with nephroblastoma?
Better prognosis, with <1 year of age having 80% overall 5 year survival ## Footnote Younger patients tend to respond more favorably to treatment.
28
What is neuroblastoma?
Most common extracranial tumour of childhood 80% occur in those under 4 years of age Tumour of neural crest origin (up to 50% occur in the adrenal gland) The tumour is usually calcified and may be diagnosed using MIBG scanning
29
What is angiomyolipoma?
80% of these hamartoma type lesions occur sporadically, the remainder are seen in those with tuberous sclerosis Tumour is composed of blood vessels, smooth muscle and fat Massive bleeding may occur in 10% of cases