Renal patho 1 Flashcards

1
Q

Waxy casts

A

CKD/ESRD

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2
Q

Hyaline casts

A

► via solidification of Tamm–Horsfall mucoprotein

► Reflects concentrated urine

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3
Q

Dipstick test for the presence of ____

Affected by ____

A

►heme
proteins

►urine concentration

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4
Q

Gold standard for protein evaluation in urine

A

24h urine sample

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5
Q

Spot urine test:

Purpose:

A

►Urine protein to Cr ratio
►To find out the presence or absence of protein in the urine. This may be used as a screening test for kidney disease particularly to screen diabetic nephropathy.

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6
Q

Nephritic syndrome etiology:

A

Glomerular inflammation → GBM damage → ↓filtrarion barrier → ↓GFR

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7
Q

Nephrotic syndrome- disruption of

A

Podocyte → impaired charge barrier

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8
Q

Affect of nephrotic syndrome on lymphatics

A

↑ lymphatic drainage → net plasma filtration into the interstitium (↑interstitial pressure → edema) → ↓effective circulatory volume → RAAS activation

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9
Q

MCD- immune dyregulation leads to overproduction of _____

A

glomerular permeability factor (IL-13) that directly damages podocytes

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10
Q

Focal segmental glomerulosclerosis- LM:

A

—segmental sclerosis and hyalinosis

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11
Q

Membranous nephropathy:
LM—
IF
EM

A

►diffuse capillary and GBM thickening

►granular due to immune complex (IC) deposition ►“Spike and dome” appearance of subepithelial deposits

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12
Q

_____ is the most commonly involved organ (systemic amyloidosis).

A

Kidney

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13
Q

Most common cause of death in diabetes with ESRD is

A
  1. Cardiovascular

2. Infection

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14
Q

Acute poststreptococcal glomerulonephritis

ƒ IF—

A

(“starry sky”) granular appearance (“lumpy-bumpy”) due to IgG, IgM, and C3 deposition along GBM and mesangium

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15
Q

In PSGN levels of C4 compliment is normal because compliment activation occurs via ________

A

Alternative pathway

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16
Q

In good pasture syndrome antibodies are formed against _____

A

α3 chain of type IV collagen

17
Q
Rapidly progressive (crescentic) glomerulonephritis 
 ƒ LM—
A

crescent moon shape. Crescents consist of fibrin and plasma proteins (eg, C3b) with glomerular parietal cells, monocytes, macrophages

18
Q

Diffuse proliferative glomerulonephritis

EM-

A

subendothelial, sometimes subepithelial or intramembranous IgG-based ICs often with C3 deposition

19
Q

in membranous nephropathy spikes and domes are seen on LM by?

A

Silver staining

20
Q

Membranoproliferative glomerulonephritis
► Type II is associated with ______
► Deposits

A

► C3 nephritic factor (IgG autoantibody that stabilizes C3 convertase→ persistent complement activation →↓C3 levels).
► Intramembranous deposits, also called dense deposit disease

21
Q

mixed cryoglobinemia presents as __________

A

Membranoproliferative glomerulonephritis

22
Q

D/D of lupus nephritis

How different from lupus nephritis?

A
Anemia, bone pain, kidney damage
Multiple myeloma
Waxy casts, No RBC casts
No oral ulcers
Extremely rare in young age
23
Q

Causes of calcium oxalate stones

A

►ethylene glycol (antifreeze) ingestion (↑Oxalate formation)
►vitamin C abuse (metabolized to oxalate)
►hypocitraturia (associated with ↓urine pH) , ►malabsorption (eg, Crohn disease).
► Gastric bypass surgery
► High oxalate diet green leafy vegetables, chocolates, nuts

24
Q

Lowest pH in which part of nephron

A

DCT and collecting duct

25
Q

Uric acid stone Risk factors

A

►urine volume,
►arid climates,
►acidic pH.

26
Q

Test for cystine stone

A

Sodium cyanide nitroprusside test

27
Q

Cr is elevated in obstruction _______

A

if obstruction is bilateral or if patient has an obstructed solitary kidney

28
Q

Hydronephrosis leads to

A

compression and possible atrophy of renal cortex and medulla