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23 Cards in this Set

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Re: the components of the glomerular filtration barrier:
- which is the major size barrier?
- charge barrier?
- podocytes (visceral epithelial cells)
- glomerular basement membrance
What are the two basic mechanisms of glomerular injury?
- Immune complex mediated: deposition of antigen-antibody complexes
- nonimmune complex mediated: DESTRUCTION of the functioning nephrons... scarring--> irreversible damage
Is scarring in the kidney irreversible damage?
yes.
- Nephrotic syndrome
- Asym Hematuira and recurrent gross hematuria
- nephritic syndrome
+ "rapidly progressive glomerulonephritis"
- glomerulonephritis associated with systemic dz

What are theses?
The 4 Glomerular clinico-pathologic syndromes... basically how our pts will present, in spite of whatever dz they actually have.
What is the clinical definition of nephrotic syndrome?
excessive permeability of glomerular capillary wall to plasma proteins
>3.5g protein/24hr urine.
In adults, what is the most common cause of nephrotic syndrome?
- two others?
Membranous Glomerulopathy
- immune mediated
- has primary and 2ndary forms

Focal and Segmental Glomerulosclerosis
- not immune mediated

Kidney dz associated w/ systemic dz (eg diabetes, amyloid, lupus etc.)
In children, what is the most common cause of nephrotic syndrome?
- mechanism?
Minimal change dz (70%)
- nonimmune
- injury to the podocyte (vis epithelial cell)
What are the complications of nephrotic syndrome?
-tendency to thrombosis
-propensity for infection
Only __% of all asymptomatic hematuria is of glomerular origin.

What do we do to dx?
- three possible findings?
10%; most is the bladder, prostate, urethral)

Renal biopsy
- no abnormalities (30%)
- thin basement mem dz (26%)
- IgA nephtropathy (28%)
How do we tell if blood is actually coming from an intra-renal origin?
look for dysmorphic RBCs and RBC casts in urine.
What is nephritic syndrome characterized by clinically?
Hematuria PLUS:
- elevated serum BUN and creatinine
- oliguria (decreased urine output)
- edema
- HTN
- **Proteinuria**
Lost of >50% of renal function w/i days to weeks is termed...

aka...
...Rapidly progressive glomerulonephritis.

"Crescentic glomerulonephritis"
Severe renal failure manifests clinically as...
...nausea, vomiting, hiccups, dyspnes, lethargy, pericarditis, encephalopathy, CHF, PulmEdema
What are the three major categories of RPG?

Basically, when you have Lost of >50% of renal function w/i days to weeks, you have to class it as one of 3 things.

How do you differentiate between the 3?
- immune
- Anti-GBM (glomerula basement mem) dz
- ANCA (anti-neutrophil cytoplasmic antibody) associated dz

Immunohistochem staining
circulating anti-GBM antibodies with linear glomerular IF staining is dx of what?

Glomerular immune complex localization w/ *granular* IF staining?

Little or no glomerular IF Ig staining?
anti GBM RPG.

Immune complex RPG

ANCA RPG
What are the features seen in this slide?
This is a pictures of crescentic Glom nephritis
What the 3 major categories of the tubular dz we should know?

90% of which is caused by e.coli infection?
- drug induced tubulointerstiail nephritis
- acute pyelonephritis
- Acute kidney injury / ATN

acute pyelonephritis
what is the classic triad of clinical manifestations associated with drug induced interstitial nephritis?
- seen in what % of pts with this dz?
low grade fever, skin rash, arthralgias
- 15%
What drug that pts often don't tell us about can cause:
- interstital nephritis
- nephrotic range proteinuria
- minimal change dz
NSAIDs
What are the three mechanisms of injury in drug induced tubulointerstiatial nephritis?
HyperS - synth penicillins
Nephrotoxicity - aminoglycosides
Progressive Cumulative injury - analgesic abuse
Casts of neutrophils in urine sediment is dx of what?
acute pyelonephritis
No matter what the etiology is, all thrombotic microangiopathies all cause what?

Most common etiologies? (2)
Does it matter if we catch these early?
endothelial cell injury

HUS and TTP

yes, because scarring is irreversible. Changes just in the glomeruli are less permenant than those in the vasculature.
The triad of hemolytic anemia, relative thrombocytopenia, and acute renal failure can be clinically suggestive of what?
thrombotic microangiopathies.