Renal Flashcards

1
Q

How does renal vein thrombosis present? dx?

A

infant who is dehydrated, birth depression, polycythemia, or DM mom

hx oliguria, hematuria, palpable enlarged kidneys

dx = renal US /w renal vein doppler studes

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2
Q

What are signs of lobar nephronia? How do you treat?

A

long fever curve w/ antibitoics

treat: prolonged IV and PO abx

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3
Q

What are signs of urolithiasis? diagnose?

A

obstructive sx w/ dysuria, urgency, frequency

dx: non contrast CT to dx # and location of stones and check for hydronephrosis

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4
Q

What are signs of fanconi syndrome?

A

anorexia, polydipsia, polyuria, vomit, unexplained fevers

have glucosuria w/ normal blood sugar, phosphaturia, aminoaciduria, high urine pH, mild albuminuria

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5
Q

What is next step if you see high protein in kid’s urine?

A

repeat urine dipstick on 2 separate occasions to differentiate transient vs persistent proteinuria

once its persistent –> do 24 hr urine collection for protein + renal US

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6
Q

What is likely to present w/ painless hematuria?

A

renal papillary necrosis

normal appearing RBCs in urine

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7
Q

What are findings in acute glomerulonephritis?

A

hematuria w/ htn, proteinuria, drysmorphic RBCs, RBC casts

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8
Q

What do you see in urine in acute interstitial nephritis?l

A

lots of WBCs w/ eos, not likely to have hematuria

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9
Q

What do you see in urine in acute tubular necrosis?

A

granular casts, hematuria, renal tubular epithelial cells

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10
Q

What are sx of goodpasture? how do you dx?

A

pulmonary hemorrhage, progressive renal impairment

dx: hemosiderin laden macrophages on sputum or pulm secretions, antibodies to glomerular basement membrane

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11
Q

What are sx/signs of HUS? treat?

A

bloody diarrhea + anemia (RBC hemolysis) + thrombocytopenia (activated coagulation cascade) + renal failure (high creatinine, hematuria, proteinuria, casts)

treat: supportive w/ controlling htn, fluid/electrolyte/nutrition

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12
Q

What is treatment for post strep glomerulonephitis?

A

treat underlying infection if still present, monitor BP nd fluid restrict

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13
Q

What is type 1 (distal) RTA?

A

poor k secretion into urine due to genetic, med, autoimmune

urine pH > 5.5, low-normal K
low serum HCO3, high Cl
chronic met acidosis

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14
Q

What is treatment for rental tubular acidosis?

A

oral bicarb replacement

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15
Q

What is type 2 (proximal) RTA?

A

due to poor bicarb resorption, seen in fanconi syndrome

urine pH

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16
Q

What is type 4 RA?

A

aldosterone resistance, due to obstructive uropathy or CAH

urine pH

17
Q

What risk factor, histo finding in membranous nephropathy?

A

risks: Hep B
histo: thick BM, subepithelial spikes

18
Q

What risk factor, histo finding in FSGS nephropathy?

A

risks: HIV
histo: crescent formation

19
Q

What histo finding in minimal change nephropathy? dx? next step?

A

T cell mediated injruy to podocytes –> effacement of foot processes on EM

Dx: proteinuria, hypoalbuminuria, renal biopsy w/o microscopic change

Tx: steroids

20
Q

What does it suggest if hum/bruit at CVA and hypertension? What test/finding to dx?

A

fibromuscular dysplasia

on angiography have string of beads in renal artery

21
Q

What is next step for working up UTI in kid? who gets this?

A

US bladder/renal

-

22
Q

Who gets CVUG?

A

if abnormal renal US or

- pts

23
Q

What is most common cause of recurrent UTI?

A

vesicoureteral refleux –> can lead to hydroureter + hydronephrosis

24
Q

What is complication of VUR?

A

recurrent pyelo –> blunting calices and focal parenchymal scarring

more prone to renal insufficiency, ESRD