Clinical - Glomerular Disease Flashcards

(35 cards)

1
Q

What is a urinary albumin excretion of 30-300 mg/1.7m/24 hrs?

A

Microalbuminuria

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2
Q

What is a urinary albumin excretion more than 300 mg/1.7m/24 hrs?

A

Overt proteinuria

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3
Q

What s the urinary protein value of nephrotic syndrome?

A

Urinary protein greater than 3.5g/1.73m/24hrs

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4
Q

What are the findings in nephrotic syndrome?

A

Hypoalbuminemia, peripheral edema, hypercholesterolemia, lipiduria (maltese crosses)

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5
Q

What is the thrombotic complication of nephrotic syndrome?

A

Renal vein thrombosis

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6
Q

How is the urine in nephritic syndrome?

A

Oliguria, proteinuria, urinary sediment with dysmorphic RBC

cola or smoky appearance

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7
Q

How is the urine in nephrotic syndrome?

A

Hypoalbuminemia, hypercholesterolemia, lipiduria (maltese crosses)

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8
Q

What bacteria causes post streptococcal glomerulonephritis

A

Group A beta hemolytic streptococci

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9
Q

What glomerular changes are associated with post streptococcal glomerulonephritis

A

Hypercellularity of the glomerular tufts
Subepithelial humps
Starry sky, mesangial, garland

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10
Q

What are the clinical findings in IgA nephropathy (Berger disease)

A

Microscopic hematuria and proteinuria

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11
Q

What is seen on light microscopy in IgA nephropathy

A

Mesangial expansion

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12
Q

What is seen on immunofluoresence in IgA nephropathy

A

Strong IgA staining with in the mesangium

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13
Q

How does Henock-Shonlein purpura present?

A

Microscopic or gross hematuria

RBC cast, purpura, abdominal pain

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14
Q

How does membranoproliferative glomerulonephritis present

A

Hematuria, proteinuria, nephritic syndrome

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15
Q

What are the lab findings of membranoproliferative glomerulonephritis

A

Proliferation of mesangium and thickening of glomerular capillary wall

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16
Q

How do you treat membranoproliferative glomerulonephritis

A

Long term corticosteroid therapy

17
Q

What is rapidly progressive glomerulonephritis

A

Deterioration of renal function with active urinary sediment

Crescentic glomerulonephritis

18
Q

What is wegeners granulomatosis

A

Granulomatous inflammation involving respiratory tract and vasculitis affecting small and medium sized vessels

19
Q

What is polyarteritis nodosa vasculitis

A

Necrotizing inflammation of medium sized or small arteries without glomerulonephritis or vasculitis

20
Q

What organ system is involved in Goodpastures

A

pulmonary renal

21
Q

What antibodies are involved in Goodpastures

A

Circulating anti-GBM antibodies

22
Q

What is minimal change nephropathy

A

Absence of structural glomerular abnormalities except epithelial cell foot processes seen on electron microscopy

23
Q

What is the treatment of minimal change nephropathy

A

High dose corticosteroids

24
Q

What are the clinical features of membranous nephropathy

A

Autoantibodies to the M-type phospholipase A2 receptor
Proteinuria
Subepithelial deposits along GBM

25
What is the cause of primary membranous nephropathy
Unknown
26
What is the cause of secondary membranous nephropathy
Autoimmune disease
27
What medications can cause membranous nephropathy
NSAIDS, penicillamine
28
How do you treat membranous nephropathy
``` ACEi and ARBs originally Immunosuppresive therapies (corticosteroids and cytotoxic agents) ```
29
What is the common cause of end stage renal disease in the US
Diabetic nephropathy
30
What is the early manifestation of diabetic nephropathy
Microalbuminuria
31
What lesion on renal biopsy is pathognomonic for diabetic nephropathy
Kimmelsteil-WIlson nodules
32
How can you slow diabetic nephropathy
Tight glycemic control | ACEi or ARBs
33
Should diabetic patients with microalbuminuria start ACEi even if they are normotensive
Yes
34
When is renal biopsy necessary for a patient with diabetic nephropathy
Patients with atypical course
35
What is the immune deposit location of SLE nephritis
Glomerular capillary subendothelium and fingerprint like pattern of tubuloreticular inclusions