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49 Cards in this Set
- Front
- Back
Describe the 3 layers of the glomerulus:
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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 |
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What passes/does not pass through glom capillary membrane?
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Water, electrolytes, glucose, AAs pass easily
Proteins do not pass |
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What is the first protein to pass when the membrane is damaged? Why?
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albumin - because its the smallest
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What occurs long beore clinical proteinuria?
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microalbuminuria
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When might you normally see protein in the urine?
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after running alot
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List 3 secondary causes of glomerular disease?
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1. SLE
2. DM 3. amyloidosis |
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List the 3 cellular changes that occur in the basement membrane in glomerular disease?
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1. Proliferative
2. Sclerotic 3. Membranous |
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Describe proliferative changes you might see?
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increase in cellular components and # of cells (inflammatory or WBC response)
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Describe sclerotic changes you might see?
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increase in extracellular components - primarily collagen
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Describe Membranous changes you might see?
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incr in glom capullary wall thickness (IC deposition)
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What does "diffuse" mean?
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all glomeruli, all parts
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What does "focal" mean?
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some gomeruli
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What does "segmental" mean?
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certain segment of each glomeruli
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What does "mesangial" mean?
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affecting the mesangial cells
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What are the 2 types of immune mechanisms implicated by glomerulonephritis?
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1. injury from Abs reacting w/ Ags in the glomerulus
2. Circulating Ag-Ab complexes trapped in glomerular membrane |
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2 origins of antigens?
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1. endogenous (ex. abs to self - SLE)
2. exogenous (ex. step membrane Ags in APSGN) |
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According to Dr. Otruba - what is the second leading cause of renal failure IN THE WORLD?
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inflammation of glomerular structures
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What are the 2 triggers of glomerulonephritis?
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1. immune
2. non-immune (DM, HTN,Toxins) 3. Hereditary (Alport's syndrome) |
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Which is trigger is most common?
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immune
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What word should come to mind when you hear "nephrotic syndromes"
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subepithelial
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What is abnormal in nephrotic syndrome?
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the permeability of glomerular membranes (commonly via changes in the foot processes)
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What proteins are lost in the urine? What does that loss result in?
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Igs --> immune suppression/infnx
coag factors --> thrombosis proteins that carry blood components --> altered drug doses |
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What 4 key clinical features are found in nephrotic syndrome?
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1. massive proteinuria (>3g/24hr)
2. lipiduria 3. generalized edema 4. hyperlipidemia 5. hypoalbuminemia |
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Nephrotic syndrome is not a _________, but a _____ of ________ due to ________
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not a SPECIFIC DISEASE, but a CONSTELLATION OF CLINICAL FINDINGS due to increased permeability and loss of plasma proteins in urine
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3 causes of nephrotic syndrome?
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1. minimal change dz?
2. Focal semental glomerulosclerosis 3. Membraneous GN |
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What to do during workup?
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kidney biopsy to determine specific cause of kidney filter dz
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What is minimal change disease? What age group is it most prevalent in?
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diffuse loss of foot processes in epithelial layers (fuse together into single thin layer) - can't keep protein out of urine
Kids 2-6 |
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What is focal segmental glomerulosclerosis? Who do you see it in?
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sclerosis of some of the glomerulus
Seen in hispanic or *AA* |
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What is membranous GN? who do you see it in?
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diffuse thickening of BM from IC deposition (Ab + Ag)
Adults - most common cause of nephrotic syndrome in WHITE ADULTS |
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What word should come to mind when you hear "nephritic syndrome"?
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subENDOthelial
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Where do IC deposit in nephritic syndrome?
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subendothelial, glom BM, or in mesangium
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What is the most important factor in keeping protein and blood out of the urine?
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the epithelial cell - podocyte
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What two processes are activated by nephritic syndrome?
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1. proliferative inflammatory response
2. Inflammatory process damages capillary wall |
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What clinical findings would you see in nephritic syndrome?
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1. HTN
2. variable proteinuria 3. decr GRF --> HTN, oligura, edema |
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What is acute nephritic syndrome?
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acute proliferative damage --> capillary wall damage post-infxn or primary dz (SLE)
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Clincal features of Acute Nephritic Syndrome?
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1. sudden hematuria*
2. Proteinuria 3. Decreased GFR --> HTN (late = edema) 4. Oliguria |
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How do medications cause drug related nephropathies?
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decr blood flow, obstruction (via crystals), hypersensitivity
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What causes acute interstitial nephritis?
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drug-induced allergic reaction that promotes interstitial inflammation and tubular damage
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What causes acute tubular necrosis?
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dose-dependent direct drug toxicity on tubular epithelia
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What is the leading cause of renal failure in the US?
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nephritis = inflammation/necrosis
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What is nephritis characerized by**?
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1. hematuria/RBC casts
2. DECR GRF 3. Azotemia 4. Oliguria 5. HTN |
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What does Acute Proliferative Nephritis follow? by how many days?
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follows infxn (group A b-hemolytic strep) by 7-10d
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How is acute proliferative nephritis diagnosed? treated?
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ASO titer
symptomatic tx |
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What is the cause of rapidly progressive nephritis? treatment?
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no specific cause (poss SLE, vasculitides, goodpastures syndrome)
tx: plasmaphoresis of Abs and immunosuppressive therapy |
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What is IgA Nephropathy (Buergers Dz)? Who is it seen in?
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deposition of IGA complexes in mesangium
Asian men, 10-30yo |
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What 3 things do all Acute Kidney Injuries have in common?
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1. rapid deterioration of renal fxn
2. rapid INCR in BUN and Cr 3. Oliguria |
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What are casts?
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mold of distal nephron lumen
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when do casts form?
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when urine protein concentration is high (ex. nephrotic syndrome*)
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What are hyaline casts?
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tamm horsfall mucoprotein (gel-like) w/o cells
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