Lecture 7 Glomerular Flashcards

1
Q

what is the main reason to evaluate hematuria?

A

to rule out cancer

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

how many RBC’s per high power field is indicative of the need for further evaluation?

A

3 or more

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

1st choice for ruling out renal mass/evaluate uroepithelium (ie anatomic study)

A

multiphasic CT

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

a ____ should be preformed in all patients with hematuria that are greater than 35 years of age

A

cystoscopy

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

Extraglomerular vs glomerular hematuria on UA:
which can have clots?
which has dysmorphic RBCs?
which has RBC casts?

A

extraglomerular,
glomerular,
glomerular

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

_____ persists as episodic hematuria with RBC casts, especially following a respiratory or GI infection

A

IgA nephropathy (berger disease)

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

What does immunofluorescence show in a patient with IgA nephropathy?

A

IgA deposits in the mesangium

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

what structural disorder can cause idiopathic hematuria, besides IgA nephropathy

A

thin basement membrane disease

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

Alport syndrome is due to a mutation in _____, causing thinning and splitting of the bm. Clinical triad?

A

type 4 collagen;

sensorineural deafness, glomerulonephritis, eye problems (ie retinopathy)

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

3 types of proteinuria by origin:
_____ = increased filtration of macromolecules
____ = increased excretion of LMW proteins
_____ = increased excretion of LMW proteins, typically immunoglobulin light chains in multiple myeloma

A

glomerular, tubular, overflow

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

nephrotic syndrome is characterized by more than _____ grams of ____ per day being excreted

A

3.5, protein

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

normal levels of urinary albumin is less than ____ mg of urine albumin per gm creatinine

A

30

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

____ is often the earliest clinical manifestation of diabetic nephropathy

A

increased albuminuria

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

first thing to be done when proteinuria is detected?

A

repeat UA. if negative, then “transient proteinuria”

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

if repeat UA is positive in an adolescent, consider ____ proteinuria.

A

orthostatic ie when standing

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

first line treatment to slow progression of kidney disease

A

ACE inhibitors

17
Q

Nephrotic syndrome:

hypoalbuminemia causes _____. _____ also occurs due to the liver increasing production.

A

edema, hyperlipidemia

18
Q

Other features of nephrotic syndrome:

_____ which can cause renal vein thrombosis. infection due to loss of ____ and ____ in urine. anemia due to loss of ____

A

hypercoagulation;
Ig, complement;
EPO

19
Q

nephrotic syndrome is due to damage of the ____, affecting the filtration charge barrier

A

podocytes

20
Q

the _____ receptor is the target antigen in 80% of patients with idiopathic membranous GN

A

phospholipase A2

21
Q

Membranous nephropathy:
EM:
IF:
LM: diffuse capillary, GBM thickening

A

spike and dome appearance, subepithelial deposits;

granular pattern

22
Q

membranous nephropathy has a high incidence of ______

A

renal vein thrombosis

23
Q

minimal change disease (MCD) is also called _____

A

lipoid nephrosis

24
Q

MCD is due to ____ of foot processes. it is the most common cause of nephrotic syndrome in ____. treatment is what

A

effacement;
children;
corticosteroids

25
Q

_____ is the most common cause of nephrotic syndrome in blacks and hispanics. thought to be due to a ____ variation at the APOL-1 on chromosome 22

A

focal segmental Glomerular sclerosis(FSGS);

allelic

26
Q

FSGS can occur secondary to ____ infection, ____ disease, or heroin abuse

A

HIV, sickle cell

27
Q

FSGS:
LM: segmental ____ and _____

A

scelrosis, hyalinosis

28
Q

light chain cast nephropathy is a tubular disease that is the most common renal involvement in _____

A

myeloma

29
Q

Amyloidosis:

____ stain shows _____ _____ under polarized light

A

congo red, apple-green birefringence

30
Q

____ amyloid is the most common. 50 percent of the time is is associated with meyloma. it is composed of fragments of monoclonal ____ ____

A

AL, light chain

31
Q

____ amyloid is due to fragments of an acute phase reactant. it is seen in systemic _____ disease such as rheumatoid arthritis

A

AA;

inflammatory

32
Q

diabetic glomerulonephropathy:

LM: _____ expansion, GBM thickening, eiosinophilic nodular glomerular sclerosis (aka ______ lesions)_

A

mesangial; kimmelstiel-wilson