Nephritic/Nephrotic Flashcards

1
Q

RBC Casts show?

A

Glomerulonephritis, Malignant HTN

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2
Q

WBC Casts show?

A

Acute pyelonephritis, transplant rejection

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3
Q

Granular (muddy brown) Casts show?

A

Acute Tubular Necrosis

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4
Q

Waxy Casts show?

A

End-stage renal disease/chronic renal failure

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5
Q

Black Urine shows?

A

Alkaptonuria

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6
Q

Pink/Red Urine shows?

A

Porphyria

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7
Q

Brown/Tea colored urine shows?

A

Hyperbiliruinemia

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8
Q

2 Weeks after infection of pharynx and skin patient presents with periorbital edema and cola-colored urine?

A

A PSGN

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9
Q

PSGN EM?

A

Subepithelial immune complex deposition

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10
Q

PSGN virulence factor? What is its MOA?

A

M protein-Nephritic StrainMOA: prevents Munching/Phagocytosis

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11
Q

PSGN HSR?

A

Type 3 HSR

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12
Q

PSGN Labs?

A

Increased anti-DNase B titers Decreased Complement Levels

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13
Q

PSGN Treatment and Complication?

A

Tx: supportiveComplication: RPGN

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14
Q

RPGN LM and IF?

A

Crescent Moon shaped

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15
Q

RPGN Prognosis?

A

Poor

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16
Q

What is inside the RPGN Crescent Moon shape IF/LM?

A

Fibrin and macrophages

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17
Q

MOA of Nephritic Syndrome?

A

Immune complex deposition that leads to Inflammed glomeruli+release C5a=>attracts neutrophils=>damaged and hypercellular glomeruli

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18
Q

How do should you group Nephritic Syndromes?

A

Linear=> good pasture
Granular=>PSGN, Diffuse
Negative=>WeCener, Churg, Microscopic

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19
Q

Hematuria, Hemoptysis and Sinuitis is unique to?

A

WeCeners

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20
Q

Diffuse proliferative glomerulonephritis (DPGN) MC cause?

A

SLE

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21
Q

DPGN LM?

A

Wire looping

22
Q

IgA nephropathy (Berger disease) Presentation?

A

renal insufficiency or acute gastroenteritis with Episodic hematuria with RBC casts

23
Q

IgA nephropathy is related to what vasculitis?

A

Renal pathology of Henoch-Schönlein purpura.

24
Q

MC nephropathy world wide?

A

IgA nephropathy (Berger disease)

25
What will you see in IF?
IF—IgA-based IC deposits in mesangium.
26
Alport syndrome MOA?
Type 4 (Flip the Al in alport)=> thinning and splitting of glomerular basement membrane
27
Alport Syndrome Genetics?
Most commonly X-linked.
28
Alport Triad?
Can't see, Can't pee and Can't Hear High C
29
EM for Alport?
“Basket-weave” appearance on EM.
30
Any word that has membrano means?
Thickening membrane
31
MPGN type 1 shows?
subendothelial "tram-track” appearance on PAS stain
32
MPGN type 2 shows?
intramembranous IC deposits; “dense deposits"
33
Type 1 is secondary to?
Hep B or C infection
34
Type 2 is associated with?
C3 factor=> stabilizes C3 convertase=>decreases 􏰂􏰁serum C3 levels
35
Nephrotic Syndrome, What are the groupings?
MCD and FSGS=>Effacement of foot process Membranous nephropathy/ MPGN=>1. Thickened membrane 2. Cause: immune deposition DM/Amyloidosis=>amyloid/glucose deposition
36
FSGS is MC nephrotic syndrome in?
AAs, Hispanics, HIV, Sickle Cell and Heroin
37
MCD to describe in one phrase?
Change is so MINIMAL that you only lose ALBUMIN NOT gammaglobin
38
MCD is MC nephrotic Syndrome in?
Kids
39
MCD LM?
Normal Glomeruli
40
MCD and FSGS both have?
=>Effacement of foot process
41
MCD is associated with?
Hodgkins Lymphoma
42
MCD Tx?
STeriods
43
Membranous Nephropathy EM?
Spike and Dome Appearance
44
MCC of Nephrotic Syndrome in SLE?
Membranous Nephropathy
45
Membranous Nephropathy is MCC of nephrotic syndrome in?
Caucasian adults
46
In amyloidosis, what is the LM?
Congo red stain shows apple-green
47
In amyloidosis what is the most commonly involved organ?
Kidney
48
In Diabetic Glomerulonephropathy, MOA?
Nonenzymatic Glycosylation of GBM
49
What nodules will you see?
Kimmelsteil-Wilson Lesions
50
What is the first change you will see in diabetic glomerulonephropathy?
NEG of efferent arterioles=>Increased GFR􏰂=>mesangial expansion.