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49 Cards in this Set

  • Front
  • Back
Describe the 3 layers of the glomerulus:
1. Endothelial layer - lines inner surface of capillry
2. Basement Membrane - determines permeability
3. Epithelial Layer - surrounds outer surface of bowman's capsule, attaches via foot processes to BM
What passes/does not pass through glom capillary membrane?
Water, electrolytes, glucose, AAs pass easily

Proteins do not pass
What is the first protein to pass when the membrane is damaged? Why?
albumin - because its the smallest
What occurs long beore clinical proteinuria?
microalbuminuria
When might you normally see protein in the urine?
after running alot
List 3 secondary causes of glomerular disease?
1. SLE
2. DM
3. amyloidosis
List the 3 cellular changes that occur in the basement membrane in glomerular disease?
1. Proliferative
2. Sclerotic
3. Membranous
Describe proliferative changes you might see?
increase in cellular components and # of cells (inflammatory or WBC response)
Describe sclerotic changes you might see?
increase in extracellular components - primarily collagen
Describe Membranous changes you might see?
incr in glom capullary wall thickness (IC deposition)
What does "diffuse" mean?
all glomeruli, all parts
What does "focal" mean?
some gomeruli
What does "segmental" mean?
certain segment of each glomeruli
What does "mesangial" mean?
affecting the mesangial cells
What are the 2 types of immune mechanisms implicated by glomerulonephritis?
1. injury from Abs reacting w/ Ags in the glomerulus

2. Circulating Ag-Ab complexes trapped in glomerular membrane
2 origins of antigens?
1. endogenous (ex. abs to self - SLE)
2. exogenous (ex. step membrane Ags in APSGN)
According to Dr. Otruba - what is the second leading cause of renal failure IN THE WORLD?
inflammation of glomerular structures
What are the 2 triggers of glomerulonephritis?
1. immune
2. non-immune (DM, HTN,Toxins)
3. Hereditary (Alport's syndrome)
Which is trigger is most common?
immune
What word should come to mind when you hear "nephrotic syndromes"
subepithelial
What is abnormal in nephrotic syndrome?
the permeability of glomerular membranes (commonly via changes in the foot processes)
What proteins are lost in the urine? What does that loss result in?
Igs --> immune suppression/infnx
coag factors --> thrombosis
proteins that carry blood components --> altered drug doses
What 4 key clinical features are found in nephrotic syndrome?
1. massive proteinuria (>3g/24hr)
2. lipiduria
3. generalized edema
4. hyperlipidemia
5. hypoalbuminemia
Nephrotic syndrome is not a _________, but a _____ of ________ due to ________
not a SPECIFIC DISEASE, but a CONSTELLATION OF CLINICAL FINDINGS due to increased permeability and loss of plasma proteins in urine
3 causes of nephrotic syndrome?
1. minimal change dz?
2. Focal semental glomerulosclerosis
3. Membraneous GN
What to do during workup?
kidney biopsy to determine specific cause of kidney filter dz
What is minimal change disease? What age group is it most prevalent in?
diffuse loss of foot processes in epithelial layers (fuse together into single thin layer) - can't keep protein out of urine

Kids 2-6
What is focal segmental glomerulosclerosis? Who do you see it in?
sclerosis of some of the glomerulus

Seen in hispanic or *AA*
What is membranous GN? who do you see it in?
diffuse thickening of BM from IC deposition (Ab + Ag)

Adults - most common cause of nephrotic syndrome in WHITE ADULTS
What word should come to mind when you hear "nephritic syndrome"?
subENDOthelial
Where do IC deposit in nephritic syndrome?
subendothelial, glom BM, or in mesangium
What is the most important factor in keeping protein and blood out of the urine?
the epithelial cell - podocyte
What two processes are activated by nephritic syndrome?
1. proliferative inflammatory response
2. Inflammatory process damages capillary wall
What clinical findings would you see in nephritic syndrome?
1. HTN
2. variable proteinuria
3. decr GRF --> HTN, oligura, edema
What is acute nephritic syndrome?
acute proliferative damage --> capillary wall damage post-infxn or primary dz (SLE)
Clincal features of Acute Nephritic Syndrome?
1. sudden hematuria*
2. Proteinuria
3. Decreased GFR --> HTN (late = edema)
4. Oliguria
How do medications cause drug related nephropathies?
decr blood flow, obstruction (via crystals), hypersensitivity
What causes acute interstitial nephritis?
drug-induced allergic reaction that promotes interstitial inflammation and tubular damage
What causes acute tubular necrosis?
dose-dependent direct drug toxicity on tubular epithelia
What is the leading cause of renal failure in the US?
nephritis = inflammation/necrosis
What is nephritis characerized by**?
1. hematuria/RBC casts
2. DECR GRF
3. Azotemia
4. Oliguria
5. HTN
What does Acute Proliferative Nephritis follow? by how many days?
follows infxn (group A b-hemolytic strep) by 7-10d
How is acute proliferative nephritis diagnosed? treated?
ASO titer

symptomatic tx
What is the cause of rapidly progressive nephritis? treatment?
no specific cause (poss SLE, vasculitides, goodpastures syndrome)

tx: plasmaphoresis of Abs and immunosuppressive therapy
What is IgA Nephropathy (Buergers Dz)? Who is it seen in?
deposition of IGA complexes in mesangium

Asian men, 10-30yo
What 3 things do all Acute Kidney Injuries have in common?
1. rapid deterioration of renal fxn
2. rapid INCR in BUN and Cr
3. Oliguria
What are casts?
mold of distal nephron lumen
when do casts form?
when urine protein concentration is high (ex. nephrotic syndrome*)
What are hyaline casts?
tamm horsfall mucoprotein (gel-like) w/o cells