Urological disorders (46) Flashcards

1
Q

What are the normal functions of the kidney and what happens in kidney dysfunction?

A
  1. filtration–> failure leads to accumulation of waste substance, haematuria and proteinuria, low serum protein e.g. albumin
  2. control of salt and water balance–> hypertension, water retention (sometimes dehydration)
  3. control of acid/base balance–> metabolic acidosis
  4. hormones (erythropoietin production)–> anaemia bc dec. Hb production
  5. vitamin D (1-alpha hydroxylation of vit D)–> vit D deficiency and secondary hyperparathyroidism
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2
Q

What are possible locations and pathogens for infections in the urinary tract?

A
  • bladder= cystitis
  • kidney= pyelonephritis
  • bacteria most common
  • virus and fungus in immunocompromised patients
  • pathogen enters causing inflammation
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3
Q

How do we diagnose a urinary tract infection?

A
  • history
  • physical examination
  • urine dipstick
  • urine microscopy, culture and sensitivity
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4
Q

How do we treat a urinary tract infection?

A
  • antibiotics: depending on severity of illness, most common bacteria in local area, modified when sensitivity from urine culture is available
  • pain control
  • supportive care e.g. rehydration
  • consider imaging if other factors or differential diagnosis
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5
Q

How can the immune system damage the kidney?

A

via antibodies or inflammatory cells (neutrophils, monocytes/macrophages, T cells)

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6
Q

How will an inflammatory condition with an immunological cause present clinically?

A
  • nephritic syndrome
  • proteinuria
  • nephrotic syndrome
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7
Q

What is glomerulonephritis?

A

inflammation of the microscopic filtering units of the kidney (glomeruli)

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8
Q

How do we diagnose an inflammatory condition with an immunological cause?

A
  • history and physical examination
  • urine test
  • blood test incl. immunology tests
  • imaging: start w/ ultrasound
  • kidney biopsy
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9
Q

What are the signs of nephritic syndrome?

A
  • haematuria (blood in urine)
  • variable amount of proteinuria
  • may have hypertension, reduced urine output, inc. urea and creatinine
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10
Q

How do we diagnose nephritic syndrome?

A
  • history physical examination
  • urine dipstick
  • urine microscopu
  • urine protein:creatinine ratio
  • blood tests: kidney function and immunology test
  • kidney biopsy
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11
Q

What is IgA nephropathy?

A
  • most common primary glomerulonephritis
  • v high prevalence in far east
  • deposition of IgA antibody in kidney , only detected by biopsy
  • inflammation and scarring
  • about 30% progress to kidney failure
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12
Q

How do we treat IgA nephropathy?

A

supportive:

  • treat hypertension and reduce proteinuria using ARB or ACEI
  • reduce sodium intake
    immunotherapy: many different choices, ongoing clinical trials
  • renal replacement therapy–> at late stage : kidney transplantation or dialysis
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13
Q

What is an example of a disease that affects the kidney and lung specifically?

A
  • Goodpasture’s disease
  • antibody mediated anti-glomerular basement membrane (autoantibody)
  • bc shared common antigen between lung and kidney
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14
Q

What are examples of diseases that affect multiple organs/tissues?

A
  • systemic lupus erythematosus (SLE) caused by autoantibodies e.g. antinuclear factor, anti-dsDNA
  • vasculitis caused by autoantibodies called ANCAs
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15
Q

What is diabetic nephropathy?

A

most common cause of chronic kidney disease and kidney failure in west
- pathogenesis: inflammation and fibrosis (deposition of extracellular matrix in glomerulus)

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16
Q

What are the clinical features of diabetic nephropathy?

A
  • microalbuminuria
  • proteinuria
  • association w/other diabetic complications e.g. diabetic retinopathy
17
Q

How is diabetic nephropathy treated?

A
  • optimised diabetic control
  • optimised treatment of hypertension
  • stop smoking
  • reduce proteinuria using ARB or ACEI
  • new clinical trials: SGLT2 inhibitor
  • transplantation
  • dialysis
18
Q

What are risk factors for diabetic nephropathy?

A
  • hypertension
  • poor diabetic control
  • smoking
19
Q

What are the clinical signs of a nephrotic syndrome?

A
  • peripheral oedema
  • severe proteinuria
  • low serum albumin
  • variable amount of microscopic haematuria
  • associated w/ hyperlipiaemia
20
Q

How do we diagnose nephrotic syndrome?

A
  • history
  • physical examination
  • urine dipstick
  • urine microscopy
  • urien protein:creatinine ratio
  • blood tests: kidney function and immunology test
  • kidney biopsy
21
Q

What are causes of nephrotic syndrome?

A
  • minimal change glomerulopahty
  • membranous nephropathy
  • focal segmental glomerulosclerosis
  • lupus nephritis
  • otherssss
    leaking of protein…
22
Q

How do we treat nephrotic syndrome?

A
  • immunotherapy
  • diuretics to reduce peripheral oedema
  • prevent thrombosis w/ anticoagulation
23
Q

What are the possible locations of obstructive stones?

A
  • kidney
  • ureter
  • bladder
24
Q

How do stones present?

A
  • pain in abdomen, back loin
  • blood in urine
  • associated w/ urine infection
  • about 90% of kidney stones are radio-opaque
25
Q

How do we treat stones?

A

supportive:
- pain control
- hydration
specific treatment:
- shockwave lithotripsy–> high energy sound waves to break up large kidney stones
- utereoscopy through urethra, bladder and ureter
- percutaneous nephrolithotomy–> small percutaneous incision, insertion of nephroscope, stone is removed

26
Q

What benign condition can be seen in the urinary tract?

A

benign prostatic hypertrophy

27
Q

What malignant conditions can be seen in the urinary tract?

A
  • kidney: renal cell carcinoma
  • ureter and bladder: transitional cell carcinoma
  • prostatic cancer
  • testicular cancer
28
Q

How do neoplastic conditions present clinically?

A
  • asymptomatic (incidental finding during other investigation)
  • haematuria
  • pain
29
Q

What investigations are used to detect neoplastic conditions?

A
  • imaging (ultrasound, CT and/or MRI)
  • urine cytology
  • blood test for marker: prostatic specific antigen
  • kidney function
  • histological diagnosis by biopsy or excised tumour
  • staging studies: any evidence of metastasis
30
Q

How are neoplastic conditions treated?

A
  • to release any obstruction of the urinary tract: nephrostomy, bladder catheter and/or surgery
  • chemotherapy
  • radiotherapy
  • hormonal therapy for hormone sensitive cancer e.g. prostate
  • surgery
31
Q

What are the different types of polycystic kidney and their inheritance patterns?

A
  • neonatal: autosomal recessive
  • adult onset: autosomal dominant
  • some patients have no family history
32
Q

What are the consequences of polycystic kidneys?

A
  • loss of kidney function
  • pain
  • bleeding into renal cysts (bc has vessels)
  • infection of renal cysts
  • asymptomatic in some patients
33
Q

How is polycystic kidney disease treated?

A
  • new medication: tolvaptan- vasopressin receptor 2 antagonist- to slow down cyst formation
  • treat hypertension and infection
  • pain control
  • renal replacement therapy: transplantation and dialysis
34
Q

How can we detect a horseshoe kidney?

A

imaging of abdomen/pelvis

35
Q

What are the consequences of horseshoe kidney?

A

inc. risk of
- obstruction
- stones
- infection