19-20 Flashcards

1
Q

What is the most frequent lesion associated with carcinoma? It is also the most common cause of nephrotic syndrome in elderly and adults..

A

Membranous glomerulopathy

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

Membranous glomerulopathy is most common in what populations?

A

Middle aged males

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

Most pts with membranous glomerulopathy present with Cr that is ___

A

Normal to slightly elevated

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

Spontaneous vascular thrombosis is most common with ____. Which 3 kinds of vascular thrombosis are common?

A

Membranous glomerulopathy

  • renal vein thrombosis
  • PE
  • DVT
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Hallmark lab findings for membranous glomerulopathy is ___

*what else can you find

A

Nephrotic proteinuria

*complement levels normal, elevated LDL and VLDL, enhanced hyoercoagulable state

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

Staging of membranous glomerulopathy

A
  1. Subepithelial deposits
  2. Basement membrane starts to project between deposits
  3. Basement membrane envelops deposits
  4. Thickened BM with irregular lucent zones
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Tx for membranous glomerulopathy

A

Alternating courses of steroids and chlorambucil

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

___ is characterized by persistent antigenemia and circulating immune complexes with glomerular depositions.

  • lesions in mesangium and capillary wall
  • widening of capillary loops with double contour
  • in older adults it is associated with hep c
A

Membranoproliferative Glomerulonephritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Type I vs Type II membranoproliferative GN

A

I- hep C

II- dense deposit disease, rare, poor prognosis, C3 NeF

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

___ is a characteristic feature of all types of membranoproliferative GN

A

Low complement levels

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

Tx for membranoproliferative GN

A
  • Type I- treat underlying disease (cytoxan of MMF plus prednisone for 6 months)
  • Type II-good therapy is lacking
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Rapidly progressive GN is also called ___

A

Crescentic GN

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

Tx for Rapidly progressive GN

A

SoluMedrol IV for 3 days
Cytoxan and prednisone
*treat aggressively

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

___ is the most common GN in the world. Common symptoms are hematuria. Much more common in males

A

Berger disease

Aka IgA nephropathy

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

Lab tests for dx of IgA nephropathy

A

None

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

Deposits are where in IgA nephropathy?

A

Mesangium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Tx for IgA nephropathy?

A
  • ACEI and ARB for mild disease
  • steroids or fish oil if at least proteinuria 1g/day
  • cytotoxic agents for progressive disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Chrug Strauss disease:

A

Eosinophils
Resp tract
Necrotizing vasculitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Wegeners disease:

A

Necrotizing vasculitis

Resp. tract

20
Q

Microscopic polyangitis:

A

Necrotizing vasculitis

21
Q

cANCA is most prominent in ___ disease.

22
Q

Treatment for wegeners disease

A

Prednisone
Cytoxan
Plasmapharesis
Rituxan

23
Q

Goodpastures syndrome is associated with ____ GN and ___

A

Crescenteric
Alveolar hemorrhage
Linear IgA deposits

24
Q

Goodpasture syndrome may present like wegeners, but differences include:

A

pANCA instead of cANCA

25
Treatment of goodpasture syndrome
Plasma exchange Steroids Cyclophosphamide
26
Primary vs secondary glomerular disease
1. Involves only kidney | 2. Systemic disorder
27
The more severe the damage to the GBM, the more ___
HMW proteins in the urine (ex IgG)
28
Albumin:Cr ratio (ACR) in mg/mmol 1. Mild increase = 2. Moderate = 3. Severe = Albumin:Cr ratio (ACR) in mg/g 1. Mild increase = 2. Moderate = 3. Severe =
1. <3 2. 3-30 3. >30 1. <30 2. 30-300 3. >300
29
Isolated proteinuria can be caused by: 1. 2. 3.
1. Overflow/overproduction (myeloma, negative dipstick) 2. Tubular dysfunction (Fanconi's syndrome) 3. Glomerular dysfunction
30
Mild isolated proteinuria (<1gm/day) Also called Functional Proteinuria Type of syndrome? Causes?
Glomerular syndromes - Fever - exercise - CHF * benign
31
___ is when proteinuria is absent in recumbent position. It is more common in ___. This is a glomerular syndrome
``` Orthostatic proteinuria (<1gm/day) Children and adolescents ```
32
For fixed non-nephrotic proteinuria, what do you do when: 1. Proteinuria is <1 g/day 2. Proteinuria is 1-2 g/day 3. Proteinuria is >3 g/day
1. Monitor 2. Biopsy or just monitor 3. Def biopsy
33
___ is characterized by microscopic RBCs distorted by osmotic/chemical stress as they pass through the nephron
Glomerular hematuria
34
The most common causes of asymptomatic hematuria are ___
IgA nephropathy and | Thin Basement Membrane Nephropathy
35
Nephrotic syndrome is characterized by ___ | *most common causes?
3.5 g/day protein Hypoalbuminemia *membranous nephropathy and focal segmental glomerulosclerosis
36
Nephritic syndrome
<3 g/day protein Hematuria Oliguria Abrupt onset
37
Most common causes of nephritic syndrome are ___
Crescenteric GN Endocapillary Proliferative GN IgA nephropathy
38
List of primary glomerular diseases
``` Minimal change disease Focal segmental glomerulosclerosis Membranous nephropathy Membranoproliferative GN Rapidly progressive GN IgA nephropathy ```
39
Minimal change disease is most common in ____. It is most likely a consequence of ___. It is a ____, injury leads to changes in actin cytoskeleton that causes effacement of podocytes.
1. Children less than 10 2. T-cell abnormalities which increase glomerular permeability 3. Podocytyopathy
40
___ is the major structural correlate of nephrotic proteinuria.
Minimal change disease | Podocytyopathy
41
Clinical symptoms of minimal change disease
``` Abrupt onset of nephrotic syndrome Avg proteinuria 10g/day HTN in elderly Increased sed rate, lipids Normal renal function ```
42
Treatment for minimal change disease | Also tx for Focal segmental glomerulosclerosis
Prednisone Glucocorticoids Cyclosporin if steroid-resistant
43
What is the most common lesion associated with Nephrotic syndrome?
Focal segmental glomerulosclerosis
44
What is the most common GN leading to ESRD?
Focal segmental glomerulosclerosis
45
Pathogenesis of Focal segmental glomerulosclerosis
Podocytyopathy that is NOT reversible with steroids. Viral-HIV Drugs-interferon
46
Hallmark feature of Focal segmental glomerulosclerosis is ___
Proteinuria Nephrotic syndrome A lot have hematuria