Major Glomerulonephritides table 20-5 Flashcards

1
Q

Disease: Postinfectious glomerulonephritis

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A
  1. Most Frequent clinical presentation: Nephritic syndrome
  2. Pathogenesis Immune complex mediated: circulating or planted antigen
  3. Glomerular pathology by
    1. light microscopy: Diffuse endocapillary proliferation; leukocytic infiltration
    2. flourescence micropscopy: Granular IgG and C3 in GBM and mesangium; Granular IgA in some cases
    3. electron microscopy: Primarily subepithelial humps; subendothelial deposits in early disease stages.
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2
Q

Disease: Goodpasture syndrome

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A
  1. Most Frequent clinical presentation: Rapidly progressive glomerulonephritis
  2. Pathogenesis : Anti-GBM COL4-A3 antigen
  3. Glomerular pathology by:
    1. light microscopy:
      1. Extracapillary proliferation with crescents
      2. necrosis
    2. flourescence micropscopy:
      1. Linear IgG and C3
      2. fibrin in crescents
    3. electron microscopy :
      1. No deposits
      2. GBM disruptions
      3. fibrin
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3
Q

Disease: Chronic glomerulonephritis

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A
  1. Most Frequent clinical presentation: Chronic renal failure
  2. Pathogenesis; Variable
  3. Glomerular pathology by:
    1. light microscopy: Hyalinized glomeruli
    2. flourescence micropscopy: Granular or negative
    3. electron microscopy: none
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4
Q

Disease: Membranous nephropathy

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A
  1. Most Frequent clinical presentation: Nephrotic syndrome
  2. Pathogenesis : In situ immune complex formation; PLA 2-R antigen in most cases of primary disease mostly unknown
  3. Glomerular pathology by:
    1. light microscopy: Diffuse capillary wall thickening
    2. flourescence micropscopy: Granular IgG and C3; diffuse
    3. electron microscopy : Subepithelial deposits
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5
Q

Disease: Minimal change disease

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A
  1. Most Frequent clinical presentation: Nephrotic syndrome
  2. Pathogenesis : Unknown; loss of glomerular polyanion; podocyte injury
  3. Glomerular pathology by
    1. light microscopy: Normal; lipid in tubules
    2. flourescence micropscopy: Negative
    3. electron microscopy : Loss of foot processes; no deposits
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6
Q

Disease: Focal segmental glomerulosclerosis

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A
  1. Most Frequent clinical presentation: Nephrotic syndrome; nonnephrotic proteinuria
  2. Pathogenesis:
    1. Unknown
    2. Ablation nephropathy
    3. Plasma factor (?); podocyte injury
  3. Glomerular pathology by
    1. light microscopy: Focal and segmental sclerosis and hyalinosis
    2. flourescence micropscopy: Focal; IgM + C3 in many cases
    3. electron microscopy: Loss of foot processes; epithelial denudation
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7
Q

Disease: Membranoproliferative glomerulonephritis (MPGN) type I

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A

Disease

  1. Most Frequent clinical presentation: Nephrotic/nephrotic syndrome
  2. Pathogenesis: immune complex
  3. Glomerular pathology by
    1. light microscopy: Mesangial proliferative or membranoproliferative patterns of proliferation; GBM thickening; splitting
    2. flourescence micropscopy: IgG ++ C3; C1q ++ C4
    3. electron microscopy: Subendothelial deposits
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8
Q

Disease: Dense-deposit disease (MPGN type II)

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A
  1. Most Frequent clinical presentation: Hematuria
    Chronic renal failure
  2. Pathogenesis: Autoantibody; alternative complement pathway
  3. Glomerular pathology by
    1. light microscopy:Mesangial proliferative or membranoproliferative patterns of proliferation; GBM thickening; splitting
    2. flourescence micropscopy: C3; no C1q or C4
    3. electron microscopy: Dense deposits
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9
Q

Disease: IgA nephropathy

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A
  1. Most Frequent clinical presentation: Recurrent hematuria or proteinuria
  2. Pathogenesis: Unknown
  3. Glomerular pathology by
    1. light microscopy: Focal mesangial proliferative glomerulonephritis; mesangial widening
    2. flourescence micropscopy: IgA ± IgG, IgM, and C3 in mesangium
    3. electron microscopy: Mesangial and paramesangial dense deposits
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10
Q

Disease

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
A

Disease

  1. Most Frequent clinical presentation
  2. Pathogenesis
  3. Glomerular pathology by
    1. light microscopy
    2. flourescence micropscopy
    3. electron microscopy
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11
Q

Disease

Most Frequent clinical presentation

Pathogenesis

Glomerular pathology by light microscopy, flourescence micropscopy, electron microscopy

A

Disease

Most Frequent clinical presentation

Pathogenesis

Glomerular pathology by light microscopy, flourescence micropscopy, electron microscopy

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12
Q

Disease

Most Frequent clinical presentation

Pathogenesis

Glomerular pathology by light microscopy, flourescence micropscopy, electron microscopy

A

Disease

Most Frequent clinical presentation

Pathogenesis

Glomerular pathology by light microscopy, flourescence micropscopy, electron microscopy

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13
Q

Disease

Most Frequent clinical presentation

Pathogenesis

Glomerular pathology by light microscopy, flourescence micropscopy, electron microscopy

A

Disease

Most Frequent clinical presentation

Pathogenesis

Glomerular pathology by light microscopy, flourescence micropscopy, electron microscopy

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14
Q
A
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15
Q

light microscopy: Diffuse capillary wall thickening

flourescence micropscopy: Granular IgG and C3; diffuse

electron microscopy : Subepithelial deposits

A

Membranous nephropathy

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