Approach to Glomerular Disease Flashcards

1
Q

What kind of sediment has RBC casts, RBCs, WBCs, and variable proteinuria in range of 2-6 gms?

A

nephritic urinary sediment

RBC casts are pathognomonic of active glomerulonephritis

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

What kind of sediment has heavy proteinuria, oval fat bodies, fatty casts and free fat droplets?

A

nephrotic urinary sediment

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

What are Palmer’s five clinical syndromes affecting the glomerulus?

A
chronic glomerulonephritis
nephrotic syndrome
acute glomerulonephritis (abrupt onset of nephritic)
RPGN
asymptomatic hematuria and proteinuria
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are key differences between the presentations of nephritic syndrome and nephrotic syndrome?

A

nephritic is primary Na retention, nephrotic is secondary
HTN more common in nephritic
circulatory congestion (CHF) only in nephritic
GFR more severly reduced in nephritic

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

What is chronic glomerulonephritis?

A

progressive renal failure insidious in onset with varying degrees of hematuria, proteinuria and HTN
Difficult to determine what primary cause was

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

What lab and physical findings are present with chronic glomerulonephritis?

A

nonspecific urinalysis

small kidneys

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

What specific organisms are people with nephrotic syndromes more vulnerable to?

A

encapsulated gram positives

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

How can acute glomerulonephritis be distinguished from RPGN?

A

GFR declines more rapidly in RPGN

acute often associated with preceding inf and can spontaneously resolve

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

What creatinine change means a patient has RPGN?

A

rise of over 2 in 3 months

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

What are secondary causes that can cause MCD?

A

NSAIDs - patients usually have acute interstitial nephritis too
Hodgkins

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

If the sample obtained from a patient with FSGS has no areas of sclerosis, what can be the only clue to the diagnosis?

A

areas of tubular atrophy and interstitial fibrosis

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

What genes have been indicated to be involved in the familial form of FSGS?

A
podocin
nephrin
alpha actinin 4
TRPC6 ion channel
CD2AP
formin family of actin regulatory proteins
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What finding is associated with a particularly poor prognosis for FSGS?

A

massive proteinuria (>10/24 hrs)

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

What is HIVAN?

A

more common in black men
nephrotic syndrome, kidney insufficiency, and rapid progression to ESRD
viral inf of visceral epithelial cells
can have collapsing variant of FSGS or not

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

What are big differences with the physical findings present in HIVAN?

A

no edema or HTN
Kidneys are LARGE
tubulocystic lesions and tubuloreticular bodies on EM

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

What is frequently seen in association with dense deposit disease?

A

partial lipodystrophy

17
Q

What is the third type of MPGN?

A

similar to type 1
subepithelial deposits prominent - also has subendothelial
complex disruption of GBM with large lucent areas

18
Q

What finding is common to all types of MPGN?

A

hypocomplementemia
via classic pathway in type 1
via alternate pathway in type 2

19
Q

What is the main cause of AA amyloidosis?

A

develops secondary to chronic inflammatory states

20
Q

What is AF amyloidosis?

A

familial
abnormalities of transthyretin
also fibrinogen A alpha chain

21
Q

What do RF, RPR tests and SPEP, UPEP tests look for in the evaluation of patients with glomerular disease?

A

RF indicates Hep C
RPR tests for syphilis
SPEP, UPEP look for AL amyloid

22
Q

What is the progression of diabetic nephropathy?

A

Stage 1: renal hypertrophy and hyperfunction
Stage 2: clinically silent renal disease - BM thickening, mesangial expansion, GFR still high and no albuminuria
Stage 3: incipient nephropathy - microalbuminuria, nl GFR, no HTN
Stage 4: Overt diabetic nephropathy - decreased GFR and HTN
Stage 5: ESRD

23
Q

How can microalbuminuria be detected?

A

urine spot test
albumin/creatinine ratio between 30-300
over 300 is now macroalbuminemia