32 - Renal system 2 Flashcards

1
Q

Causes of urinary tract obstruction - pelvis

A

Calculi
Tumours
Ureteropelvic stricture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Causes of urinary tract obstruction - ureter-intrinsic

A
Calculi
Tumours
Clots
Sloughed papilae 
Inflammation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Causes of urinary tract obstruction - ureter-extrinsic

A

Pregnancy
Tumours
Retroperitoneal fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Causes of urinary tract obstruction - prostate

A

Hyperplasia
Carcinoma
Prostatitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Functional obstruction of urinary tract

A

Neurological conditions

Severe reflux

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Sequelae

A

Infection - cystitis, ascending pyelonephritis

Stone/calculi formation

Kidney damage - acute or chronic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Consequences of urinary tract obstruction dependent on…

A

Site
Degree of obstruction
Duration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Urinary tract obstruction - clinical presentation

A

Acute bilateral obstruction -> pain, acute renal failure & anuria

Chronic unilateral obstruction -> asymptomatic, but will go to cause corticol atrophy and reduced renal function

Bilateral partial obstruction -> initially polyuric with progressive renal scarring and impairment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Renal calculi/urolithiasis- epidemiology

A

7-10% of population + increasing
Male
Peak onset 20-30

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Renal calculi/urolithiasis - pathogenesis

A

Either due to excess of precipitating substances e.g. Ca

Or change in urine constituents (pH)

Poor urine output - supersaturation

Decreased citrate levels

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Renal calculi/urolithiasis - classification of stones

A
Calcium (70%) - calcium oxalate
Struvite stones (15%) - magnesium ammonium phosphate
Urate stones (5%) - uric acid
Cystine stones (1%)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Calcium stones - cause

A

Hypercalciuria due to: hypercalcaemia, excessive absorption of intestinal Ca2+, inability to reabsorb tubular Ca2+, idiopathic

Other risk factors = gout, hyperoxaluria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Causes of hypercalcaemia

A

Bone disease
PTH excess
Sarcoidosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Process of struvite stone formation

A
  1. Urease producing bacterial infection
  2. Urease converts urea to ammonia
  3. Causes a rise in urine pH
  4. Precipitation of MgNH4 phosphate salts
  5. Large ‘staghorn’ calculi

THERE IS A PICTURE OF A STAG

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Urate stones

A

Hyperuricaemia

Gout
Or patients with a high cell turnover e.g. leukaemia

Idiopathic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Cystine stones

A

Rare

Occur in the presence of an inability of kidneys to reabsorb amino acids

17
Q

Renal calculi - investigations

A

Non-contrast CT scanning (gold standard) 95% sensitive

US in pregnancy or where CT not possible (30-67% sensitive)

IV urography (70% sensitive) for stones

18
Q

Sequelae definition

A

Secondary condition so caused by another

19
Q

Sequelae for renal

A

Obstruction
Haematuria
Infection
Squamous metaplasia +/- squamous cell carcinoma

20
Q

Renal cell carcinoma

A

3% of cancers
Vast majority of renal carcinomas are clear cell
In older people M>F

21
Q

Risk factors for renal disease

A
Tobacco
Obesity
Hypertension
Oestrogens
Acquired cystic kidney disease
Asbestos exposure
22
Q

Von Hippel-Lindau Syndrome - features

A

Most common of severe cancer syndromes

VHL gene required for breakdown of hypoxia inducible factor-1 (HIF-1) oncogene

Loss of gene function causes cell growth and increased cell survival

Tumours in kidneys, blood vessels and pancreas

23
Q

Von Hippel-Lindau Syndrome - clinical presentation

A

Local symptoms - haematuria, palpable abdo mass, costovertebral pain

Incidental
Late presentation: systemic symptoms or mets

Paraneoplastic syndromes

24
Q

Paraneoplastic syndrome - what is it?

A

Clinical syndrome caused by tumours
Not related to the tissue that the tumours arose from
Not related to invasion by the tumour of itself or mets

25
Q

Paraneoplastic syndromes associated with renal cell carcinoma

A

Cushing’s (ACTH)
Hypercalcaemia (PTH related peptide)
Polycythaemia (EPO)

26
Q

Renal Cell Carcinoma - morphology

A

Clear cell: well defined yellow tumours often with haemorrhagic areas. May extend into perinephric fat or into renal vein

Papillary - more cystic more likely to multiple

27
Q

Renal Cell Carcinoma - microscopy of clear cell

A

Clear cell has clear cells - duh.
Delicate vasculature
Small bland nuclei

28
Q

Renal Cell Carcinoma - microscopy of non-clear cell

A

Papilarry tumours
Cuboidal, foamy cells
Surrounding fibrovascular cores often containing foamy macrophages or calcium

29
Q

Urothelial cell carcinoma - features

A

95% of bladder tumours
Arising from specialised multilayers epithelium
Most common in bladder but may rise from renal pelvis to urethra

30
Q

Urothelial cell carcinoma - risk factors

A

Age
Gender (M>F)

Carcinogens - smoking, arylamines, cyclophosphamide, radiotherapy

31
Q

Urothelial cell carcinoma - presentation

A

Haematuria - most common
Urinary frequency
Pain on urination
Urinary tract obstruction