Nephrology Flashcards

1
Q

what is diagnostic of goodpasture syndrome

A

linear pattern of IgG deposition against glomerular basement membrane

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2
Q

Goodpasture syndrome triad

A

acute glomerulonephritis
pulmonary alveolar haemorrhage
circulating anti GBM antibodies

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3
Q

nephronophthisis

A

AR
causes medullary cystic kidney disease (small kidneys b/l on US)
leading cause childhood ESRD
presents with polyuria and polydipsia

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4
Q

When is renal biopsy indicated in HSP

A

proteinuria - UPCR >200, increasing trend >4/52 after diagnosis
nephrotic syndrome - low alb, oedema and heavy proteinuria
nephritic syndrome - HTN, haematuria, rapidly deteriorating renal function
HTN
Macroscopic haemturia with proteinuria

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5
Q

Cystinosis

A

AR
failure to thrive
recurrent vomiting
metabolic acidosis
hypo K
dehydration

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6
Q

grade of VUR

A

I: urine tracks into ureter non dilation
II: urine tracks into renal pelvis, no dilation
III: mild-moderate dilatation of ureter only
IV: ureteral tortuosity, with pelvicalyceal dilatation
V: gross dilatation and ureteral tortuosity with blunted fornices

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7
Q

nephrotic syndrome triad

A

oedema
proteinuria
hypoalbuminaemia

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8
Q

most common type nephrotic syndrome

A

primary idopathic (90%)
of this 85-90% minimal change disease, carries best prognosis
10-15% focal segmental glomerulosclerosis 10-15%

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9
Q

management of nephrotic syndrome

A

steroids - pred minimum 16 weeks
penicillin prophylaxis
PPI

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9
Q

when is nephrotic syndrome classes as steroid resistant

A

doesn’t respond to 28days of treatment with prednisolone

all steroid resistant require biopsy

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10
Q

distal renal tubular acidosis type I vs type IV

A

I:
reduced H excretion in distal tubule
urine ph >5.5 - can never acidify
nephrocalcinosis
plasma hCO3 <10
low-normal plasma K
high urine ca/cr ratio

IV:
impaired aldosterone action causing reduced H and NH3 excretion
urine Ph >5.5
plasma HCO3 >15
high plasma K
normal urine ca/cr ratio

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11
Q

signs pre renal failure over ATN

A

return of renal function to baseline within 24-72 hrs after fluids
urinary na concentration <20

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12
Q

HSP - histology

A

small vessel vasculitis - skin, GI, kidneys and joints
deposits of IgA in mesangium

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13
Q

AD polycystic kidney disease

A

multiple renal cysts
commonest inherited nephropathy
PKD1 on chromosome 16

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