Renal Pathology Flashcards

1
Q

Compare the 4 cystic diseases of the kidney. (Don’t break down PKD on this one)

A

Simple cyst: thin walled w/ clear fluid, single or multiple, common with age. Benign.
Medullary sponge kidney: many small cysts throughout the kidney medulla. Benign.
PKD: genetic, lots of large cysts, leads to kidney failure.
Chronic dialysis cysts: pts on dialysis, smaller cysts, assoc w/ RCC

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2
Q

Adult vs Childhood PKD

A

Adult: AD, dz develops in adulthood, chronic renal failure in middle age, assoc w/ liver cysts.
Childhood: AR, dz congenital, renal failure early in life, assoc w/ fetal demise.

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3
Q

What are the three histological changes that may occur in glomerular disease?

A
  • Thickening of the glomerular basement membrane
  • Hypercellularity
  • Hyalinosis/sclerosis
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4
Q

What are the clinical characteristics of nephrotic syndrome?

A

Heavy proteinuria, hypoproteinemia, hyperlipidemia, anasarca

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5
Q

What are the clinical characteristics of nephritic syndrome?

A

PHAROH
Proteinuria, hematuria, azotemia, RBC casts, oliguria, hypertension
Immune-mediated!

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6
Q

What three diseases are characterized by nephrotic syndrome?

A

Lipoid nephrosis/minimal change disease
Membranous glomerulopathy
Focal-segmental glomerulosclerosis

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7
Q

Lipoid nephrosis

  • Is the MC…
  • Proteinuria selective/nonselective
  • Micro appearance
A
  • MC cause of nephrotic syndrome in kids (peaks age 2-3)
  • Selective proteinuria
  • Nothing on histo, no immune complexes.
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8
Q

Membranous glomerulopathy

  • Is the MC…
  • Etiology
  • Micro appearance
A
  • MC cause of nephrotic syndrome in adults
  • Immunologically mediated (Ab bind Ag in GBM –> local damage and inc permeability)
  • Thickening of capillary loops, BM may appear spiked
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9
Q

Focal-segmental glomerulosclerosis

  • Is the MC…
  • Micro appearance
A
  • MC cause of nephrotic syndrome in African Americans

- Collagenous fibrous changes leading to loss of function, affects only part (segmental) of some glomeruli (focal)

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10
Q

What is the most common cause of nephritic syndrome in the US?

A

Post-streptococcal glomerulonephritis

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11
Q

What is the most common cause of nephritic syndrome worldwide?

A

IgA Nephropathy (Berger’s disease)

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12
Q

Post-Strep glomerulonephritis

  • Definition
  • Micro appearance
  • Labs
A
  • Deposits of immune complexes trapped along basement membrane following GAS pharyngitis/impetigo
  • Hypercellularity, neutrophils, poorly defined capillary loops
  • High ASO titer
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13
Q

Crescentic glomerulonephritis

  • Definition
  • Micro appearance
A
  • Description of how some extremely acute diseases progress

- Capillary loop thickening, endothelial proliferation, crescentic figures, deposition of IgG along BM

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14
Q

IgA Nephropathy

  • Etiology
  • Micro appearance
A
  • Hypersecretion of IgA in response to infx

- Proliferation of mesangium

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15
Q

MC cause of nephrotic syndrome in kids

A

Lipoid nephrosis/Minimal change disease

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16
Q

MC cause of nephrotic syndrome in adults

A

Membranous glomerulopathy

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17
Q

MC cause of nephrotic syndrome in African Americans

A

Focal-segmntal glomerulosclerosis

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18
Q

MC cause of renal failure in US

A

Diabetic nephropathy

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19
Q

Diabetic nephropathy

  • Etiology
  • Micro appearance
A
  • Glomerular hyperfiltration –> BM & mesangial proliferation
  • nodular glomerulosclerosis
20
Q

Nodular glomerulosclerosis assoc w/ DM (special name)

A

Kimmelstiel-Wilson Disease

21
Q

Amyloidosis nephropathy

  • Etiology
  • Micro appearance
A
  • Amyloid accumulates in mesangium and capillary walls

- Amyloid is acellular, eosinophilic

22
Q

Goodpasture’s syndrome

  • Etiology
  • Micro appearance (late disease)
  • Other organ involvement
A
  • Circulating anti-basement membrane antibody
  • Crescentic figures (RPGN)
  • Respiratory
23
Q

Differentiate toxic vs ischemic acute tubular necrosis.

A

Toxic: proximal, acute, obliterated lumen
Ischemic: distal, mb acute, often dt chronic progressive atherosclerosis, skip lesions throughout tubule

24
Q

Characteristic UA finding of acute tubular necrosis (both toxic and ischemic)

A

Muddy brown casts

25
Characteristic histo finding of malignant nephrosclerosis
Blood vessels that look like onion rings
26
Gross finding of infarction vs histo finding of ischemia
Pale tissue, especially in a wedge | Poor uptake of vital stain
27
Characteristic finding of chronic cystitis
Malakoplakia
28
Characteristic histo finding of malakoplakia
Michaelis-Gutmann bodies
29
Compare AIN and analgesic nephropathy
Both are drug-induced damage to interstitium AIN is an allergic rxn to a single dose (edema, inflammatory infiltrate, thickening of BM) Analgesic nephropathy is the result of analgesic abuse (ischemic injury)
30
Give the types of renal stones. - Which is MC - Which is assoc w/ UTI - Which is assoc low urine pH - Which is MC in kids
``` Calcium oxalate (MC 75%) Triple phosphate/staghorn (2MC 15%, assoc w/ Proteus UTI) Uric acid (3MC, pH ```
31
Common cause of acute renal failure
Toxic ATN
32
MC cause of HUS
E. coli O157:H7
33
MC source of renal artery emboli
Heart
34
MC renal malignancy
RCC
35
MC primary renal tumor in kids
Wilm's tumor
36
MC cell of origin for RCC
Proximal tubule epithelium
37
MC and second MC bladder cancer
Transitional cell carcinoma | Squamous cell carcinoma
38
Very common, small renal tumor with frond-like pattern on histology.
Renal papillary adenoma
39
Renal tumor with uniform, large, polygonal cells and numerous prominent mitochondria with stacked appearance
Oncocytoma
40
Pediatric renal tumor with nests of primitive, basophilic cells and primitive nephrons on histology.
Wilm's tumor
41
Classic triad, major risk factors, and general age for RCC
- flank pain, hematuria, palpable abdominal mass - tobacco, toxic exposure, acquired cystic dz - old age
42
Gross and micro appearance of malakoplakia
Gross: pale, raised mucosal plaques Micro: large, foamy M0 with Michaelis-Gutmann bodies, multinucleated giant cells
43
Eosinophilic infiltrate in bladder
Eosinophilic cystitis
44
Pathognomonic finding in interstitial cystitis
Hunner's ulcers
45
Wegener's Granulomatosis | - Serology
C-ANCA
46
What is the appearance of the crystals in the four main renal stones?
Calcium oxalate: rectangular, like envelopes Triple phosphate: rectangular, like coffin lids Uric acid: square, rhomboid, polygonal Cystine: hexagon