Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
19 Cards in this Set
- Front
- Back
What is the primary disease that causes "Nodular Glomerulosclerosis"?
|
Diabetic Glomerulopathy
|
|
Which form of diabetes is associated w/ Diabetic Glomerulopathy?
|
Both forms;
Type 1 > Type 2 |
|
Diabetic Glomerulopathy is the most common cause of what illness in the US?
|
Chronic Renal Failure
|
|
What are the primary risk factors for diabetic glomerulopathy?
|
Poor Diet/Glycemic Control
Hypertension |
|
What is a physical exam finding that highly correlated with Diabetic Glomerulopathy? (Hint: It doesn't have anything to do directly with your kidneys)
|
Diabetic Retinopathy
|
|
What is the principle mechanism of pathogenesis in Diabetic Glomerulopathy?
|
Non-enzymatic Glycosylation of glomerulus (and even tubule)
Glucose attaches to amino acids Increases permeability to proteins |
|
Which of the renal vessels is affected first by Diabetic Glomerulopathy? What is this process called? What does this do to the GFR?
|
Efferent Arteriole
Hyaline Arteriosclerosis Decreases GFR |
|
What is a diagnostic microscopic finding of Diabetic Glomerlopathy?
|
Kimmelstiel-Wilson Nodules
Proteins and Type IV collagen trapped in the mesangial matrix |
|
What is seen on electron microscopy of Diabetic Glomerulopathy?
|
Fusion of podocytes
|
|
What is the initial laboratory finding that indicates Diabetic Glomerulopathy? When during the course of diabetes does this begin to manifest?
|
Microalbuminuria
~10 years after poor glycemic control |
|
What is the main pharmacologic treatment for Diabetic Glomerulopathy?
|
ACEI - decreases ACE constriction of efferent arterioles
|
|
What is the inheritence pattern of Alport's Disease?
|
Autosomal Dominant (perhaps X-linked?)
|
|
What is the pathogenic mechanism of Alport's Disease?
|
Auto-antibodies developed to type IV collagen in GBM (sounds like Goodpastures?)
|
|
What other defecits are associated with the genetic Alport's Syndrome?
|
Sensorineural hearing loss and abnormal ocular movements
|
|
What are the miscroscopic finding of Alport's Disease?
|
Lipid accumulation in VECs producing foams cells
|
|
What is the inheritance pattern of Thin Basement Membrane Disease?
|
Autosomal Dominant
|
|
What happens to renal function in Thin Basement Membrane Disease?
|
Normal Function - mild proteinuria, constant hematuria
|
|
List from most common to least the causes of Chronic Glomerulonephritis?
|
1. RPGN
2. FSGS 3. Type 1 MPGN 4. Membranous GN 5. Diffuse Prol. GN (SLE) 6. IgA GN |
|
What is the gross appearance of the kidneys in Chronic Glomerulonephritis?
|
Shrunken Kidneys
|