10.27: Renal I Flashcards

1
Q

2 main categories of kidney disease?

A
  1. NephrOTIC: proteinuria > 3-3.5g/day

2. NephrITIC: hematuria

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

Which form of kidney disease is hematuria a hallmark of?

A

Nephritic

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

What is frothy urine characteristic of?

A

Proteinuria (nephrotic syndrome)

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

Some causes of hematuria?

A
  1. Glomerulonephritis
  2. Carcinoma
  3. Trauma
  4. Infarct
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Characteristics of nephritic syndrome?

A
  1. Hematuria w/ dysmorphic cells and RBC casts
  2. Some degree of oliguria and azotemia
  3. Htn.
  4. Active urinary sediment
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What does active urinary sediment mean?

A

Dysmorphic RBCs or RBC casts in urine

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

What is acute postinfectious glomerulonephritis? presentation?

A
- Usually presents in children
"Acute nephritic syndrome"
1. Hematuria
2. Edema
3. Htn. 
4. Renal failure
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Normal cause for acute postinfectious glomerulonephritis? and pathology?

A
  • 1 - 4 weeks post pharyngitis from group A Beta hemolytic strep
  • These bacteria have M protein virulence factor
  • Antigen + IgG immune complexes deposit in renal capillaries activating complement C5a
  • Neutrophils are attracted causing damage
  • Damage to tissue allows RBCs to pass through leading to hematuria
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What characteristic of immune complex is unique to postinfectious glomerulonephritis?

A
  • In situ formation of immune complex leading to subepithelial “humps”
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is subepithelial humps of immune complex characteristic of?

A

Post infectious glomerulonephritis

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

What are trilobed cells?

A

Usually neutrophils

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

Laboratory tests indicative of post infectious glom.?

A
  1. Tea color, smoke, coca cola urine
  2. Hematuria w/ mild proteinuria
  3. Increased ASO titer (antistrep)
  4. Decreased complement levels
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Prognosis in acute postinfectious glomerulonephritis?

A
  1. 95% recover in children
  2. Adults can become chronic glomerulonephritis
  3. Small subset of children with gross hematuria can develop severe acute syndrome with renal failure
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

When is renal biopsy needed in acute post infectious glom.?

A
  • Only if the course is a typical

- Not if the course is typical

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

What is the main Ig in the body?

A
  • IgG

- IgA is main Ig in secretions and mucosal immunity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is Berger Disease?

A

IgA nephropathy

17
Q

Clinical presentation of IgA nephropathy?

A
  • RECURRENT hematuria
  • PAINLESS
  • Sometimes after upper respiratory tract infection
  • Last for days recurring every few months
18
Q

What is recurrent, painless hematuria characteristic of?

A

IgA nephropathy

19
Q

Pathogenisis of IgA nephropathy?

A
  • Mucosal infection leading to IgA production

- IgA immune complex deposits in mesangium

20
Q

How do complement levels present in IgA nephropathy?

A
  • IgA actives complex system at slow rate so we do not see drop
  • Drop in immune complex levels are seen in post infectious
21
Q

What is hematuria with normal complement levels characteristic of?

A

IgA nephropathy

22
Q

What is necessary for definitive diagnosis in IgA Nephropathy?

A

Kidney needle biopsy

23
Q

What is hereditary nephritis?

A
  • Mutations in glomerular basement membrane proteins
  • Often in collagen type IV
  • Alport syndrome is best known type
24
Q

Where is type IV collagen found?

A
  1. Glomerular basement membrane
  2. Eyes
  3. Ears
25
Q

Triad of symptoms in alport syndrome?

A
  1. Nephritis
  2. Nerve deafness: hearing abnormalities
  3. Eye disorders such as early cataracts
26
Q

What is Alport syndrome?

A
  • Most common form of hereditary nephritis
  • X linked
  • Triad of symptoms
27
Q

What is lamina densa splitting and basket weave lamination characteristic of?

A
  • Hereditary nephritis

- Alport syndrome

28
Q

Prognosis of hereditary nephritis?

A
  • Kidney failure at 2 - 50 years of age

- Genetic testing needed for diagnosis

29
Q

What is atypical postinfectious glomerulonephritis?

A
  • Normally we would see pharyngitis 2 weeks before

- In “A typical” this is not the case