Pedia: Renal Flashcards

0
Q

Acute PSGN follows infection which which Streptococcal serotypes

A

12 - throat

49 - skin

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

Sudden onset hematuria and flank mass in an infant of a diabetic mother. Labs reveal hemolytic anemia and thrombocytopenia

A

Renal vein thrombosis

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

Indications for renal biopsy in the evaluation of GN

A
Acute renal failure
Nephrotic syndrome
Absence of evidence of strep infection
Normal complement
Persistently low serum C3 (>3 months)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Most common chronic glomerular disease worldwide

A

IgA nephropathy

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

Treatment for IgA nephropathy

A

Primary treatment is proper BP control.
Fish oil reduces renal disease progression.
Steroids beneficial in some

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

Most common cause of acute renal failure in young children

A

Hemolytic uremic syndrome

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

Upper limit of normal protein excretion in healthy children

A

150 mg/day

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

Non pathologic causes of proteinuria

A

Postural (orthostatic)
Fever
Exercise

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

Causes of false positive proteinuria

A
Highly concentrated urine
Gross hematuria
pH > 8
Contamination with chlorhexidine or benzalkonium
Phenazopyridine therapy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the major complication of nephrotic syndrome?

A

Infection

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

What are the usual causes of spontaneous bacterial peritonitis in nephrotic syndrome?

A

Streptococcus pneumoniae

Escherichia coli

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

Causes of false negative dipstick test for hematuria

A

Formalin

High urine vitamin C

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Components of acute nephritic syndrome

A

Tea or cola-colored urine
Facial or body edema
Hypertension
Oliguria

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

Most common cause of gross hematuria

A

UTi

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

Pathognomonic feature of Alport syndrome

A

Anterior lenticonus

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

Isolated hematuria in multiple family members without renal dysfunction

A

Benign familial hematuria

16
Q

Acute PSGN develops how many weeks after a skin infection? A throat infection?

A

3 - 6 W after pyoderma

1 - 2 W after pharyngitis

17
Q

Best single antibody titer to document cutaneous strep infection

A

Anti-deoxyribonuclease B

18
Q

Classic lesion of HIV-associated nephropathy

A

Focal segmental glomerulosclerosis

19
Q

Most common cause of membranous nephropathy worldwide

A

Malaria

20
Q

Prognosis of kids with membranous nephropathy

A

20% - chronic renal failure
40% - active disease
40% - complete remission

21
Q

Both PSGN and MPGN present with hematuria and low C3. How does one differentiate between the two?

A

PSGN does not have nephrotic features. C3 levels remain low in MPGN, while it returns to normal within 2 months in PSGN.

22
Q

What are renal conditions more likely to present as rapid progressive GN? What is the unifying characteristic in these conditions?

A
  1. Systemic vasculitis
  2. HSP
  3. ANCA-mediated GN
  4. SLE
  5. MPGN

Crescents in glomeruli is the hallmark finding

23
Q

Triad of HUS

A

Microangiopathic hemolytic anemia
Renal insufficiency
Thrombocytopenia

24
Q

Infectious causes of HUS

A

Verotoxin producing E. coli
Shiga toxin prodding Shigella dysenteriae type I
Neuraminidase-producing Streptococcus pneumoniae
HIV

25
Q

Classic features of nephritic syndrome

A

Hypoalbuminemia
Edema
Hyperlipidemia

26
Q

Hallmark of idiopathic nephrotic syndrome

A

Effacement of podocyte foot processes

27
Q

Congenital nephrotic syndrome + bilateral microcoria (fixed narrowing of the pupil)

A

Pierson syndrome

28
Q

Distal and proximal RTA both present with NAGMA and growth failure. How does one differentiate the two conditions?

A

Nephrocalcinosis and hypercalciuria in distal RTA.
Phosphate and massive HCO3 wasting in proximal RTA

Urine pH low in proximal,
High in distal

29
Q

How does one differentiate Bartter from Gitelman’s syndromes?

A
  1. Hypocalciuria in Gitelman;
    Hypercalciuria in Bartter
  2. HypoMg more prominent in Gitelman
  3. Renin and aldosterone elevated in Bartter
30
Q

An adolescent presenting with hypokalemic metabolic alkalosis, with hypomagnesemia and hypocacliuria. Diagnosis?

A

Gitelman’s syndrome

31
Q

Gain of function mutation in the epithelial Na channel

A

Liddle syndrome

32
Q

Excessive NCCT-mediated salt reabsorption

A

Gordon syndrome

33
Q

Renal mass. Histo reveals granulomatous inflammation with giant cells and foamy histiocytes

A

Xanthogranulomatous pyelonephritis

34
Q

Infectious causative agents of acute hemorrhagic cystitis

A

E. coli

Adenovirus type 11 and 21

35
Q

Sterile Pyuria is seen in what conditions

A
Viral infection
Renal TB
Renal abscess
Partially treated bacterial UTI
UTI in the presence of urinary obstruction
Interstitial nephritis
Inflammation near the ureter or bladder
36
Q

Indications for voiding cystorethrogram

A

DMSA (+) scan showing acute pyelonephritis or scarring

Patient with second febrile UTI with previous negative upper tract evaluation