Pediatric hematuria and proteinuria Flashcards

1
Q

laboratory findings in nephrotic syndrome

A
  • reduced plasma protein
  • increased cholesterol, TGs, lipoproteins
  • decreased serum sodium
  • decreased total calcium
  • positive urine dipstick protein
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what are the three histologic types of primary nephrotic syndrome?

A
  • MCNS
  • FSGS
  • membranous nephropathy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is the most common cause of nephrotic syndrome in children?

A

minimal change

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

LM and EM for MCNS

A
  • LM: normal

- EM: effacement of epithelial foot processes

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

heroin use
sickle cell
diabetes

what subtype of nephrotic syndrome?

A

FSGS

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

membranous nephropathy is characterized by diffuse irregular thickening of the ____________

A

capillary walls

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

subepithelial spike and dome pattern - what subtype of NS?

A

membranous

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

what are the lab findings in membranoproliferative GS?

A
  • hypocomplementemia
  • UA: proteinuria, possible hematuria
  • IF: Ig deposits on BM
  • EM: BM thickening with double layer tram tracks
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are the secondary causes of nephrotic syndrome?**

A
  • infections
  • drugs
  • malignancies
  • other
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are the indications for renal biopsy?

A

at time of diagnosis:

  • age over 10
  • persistent or gross hematuria
  • HTN
  • renal insufficiency
  • low C3

subsequently
- persistent proteinuria

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

what is the overall treatment for nephrotic syndrome?

A
  • loop or thiazide
  • ACEI / ARB
  • statins
  • pneumococcal vaccine
  • vitamin D and calcium supplementation
  • low sodium diet
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what are the lab findings for nephritic syndrome?

A
  • increased BUN
  • increased Cr
  • UA: hematuria and proteinuria
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

glomerular origin of hematuria?

A
  • dysmorphic RBCs

- RBC casts

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

what are latency periods in pharyngitis and skin infections for PSGN?

A
  • pharyngitis: 1-2 weeks

- skin: 3-6 weeks

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

what are the lab findings in PSGN? what is the EM finding?

A
  • positive throat culture group A strep
  • elevated strep Ab titers (ASO)
  • decreased C3**
  • RBC casts
  • EM: bumpy deposits
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what are the lab findings in henoch schonlein purpura nephritis?

A
  • IgA deposition on purpura biopsy
  • increased serum IgA
  • nonspecific blood tests
  • potential normocytic anemia
17
Q

what is the most common of gross hematuria in adolescents?

A

IgA nephropathy (berger)

18
Q

what are the lab findings for IgA nephropathy?

A
  • increased serum IgA

- EM: mesangial cell proliferation

19
Q

what is the inheritance for alport?

A

X linked (incomplete)

20
Q

what are the clinical manifestations of alport syndrome?

A
  • high frequency SN hearing loss
  • anterior lenticonus
  • kidney failure 2nd or 3rd decade of life
21
Q

what are the lab findings of alport syndrome (UA, EM)?

A
  • UA: RBC casts, hematuria, proteinuria, pyuria

- EM: split basement membrane

22
Q

what is the pathology in benign familmial hematuria?

A

diffuse thinning of basement membrane