Nephritic Syndrome (20-3) Flashcards

1
Q

Nephritic Syndrome includes _____ in the glomeruli

A

Inflammation

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2
Q

What are the 4 signs of Nephritic Syndrome?

A
  1. Proteinuria < 3.5 g/day
  2. Hematuria
  3. New onset HTN
  4. Azotemia
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3
Q

What are the 4 signs of Nephritic Syndrome?

A
  1. Proteinuria < 3.5 g/day
  2. Hematuria
  3. New onset HTN
  4. Azotemia
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4
Q

All of the diseases discussed in this deck can cause?

A

Nephritic Syndrome and/or Rapidly Progressive Glomerulonephritis

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5
Q

Post-Infectious Glomerulonephritis is most commonly due to infections with what bacteria and where and in who?

A

Streptococci of the pharynx/skin in children

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6
Q

What types of streptococci are the most common causes of Post-Infectious Glomerulonephritis?

A

Group A beta-hemolytic types 12, 4, 1

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7
Q

Post-Infectious Glomerulonephritis involves the proliferation of glomerular cells with leukocyte influx. Where do these complexes deposit?

A

Subepithelial humps

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8
Q

How does Post-Infectious Glomerulonephritis look on immunofluorescence?

A

Granular

– in situ immune complex formation

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9
Q

What occurs with Rapidly Progressive Glomerulonephritis (RPGN)?

A

Rapid loss of renal function

  • -> oliguria and nephritic syndrome signs
  • -> renal failure
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10
Q

What is a hallmark of RPGN?

A

Crescents in the glomeruli

– epithelial cells + leukocytes

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11
Q

What is 1 Anti-GBM antibody disease that can cause RPGN/Nephritic Syndrome?

A

Goodpasture Syndrome

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12
Q

What are the symptoms of Goodpasture Syndrome and in what patients?

A

Pulmonary hemorrhage + renal failure in young men

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13
Q

How will Goodpasture Syndrome appear on immunofluorescence?

A

Linear

– Anti-GBM antibodies

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14
Q

Goodpasture syndrome involves Anti-GBM antibodies that are specific to what portion?

A

Non-collagenous alpha 3 unit of collagen 4

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15
Q

What are the 3 immune complex deposition diseases that can cause RPGN/Nephritic Syndrome?

A
  1. Lupus Nephritis
  2. Henoch-Schonlein Purpura
  3. IgA Nephropathy
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16
Q

What are the 3 immune complex deposition diseases that can cause RPGN/Nephritic syndrome?

A
  1. Lupus Nephritis
  2. Henoch-schonlein purpura
  3. IgA Nephropathy
17
Q

What antibodies classify Lupus Nephritis type IV?

A

Anti-dsDNA

Anti-smith

18
Q

What is a hallmark of Lupus Nephritis?

A

Wire loop

= subendothelial deposits that cause circumferential thickening of capillary wall

19
Q

What is a hallmark of Lupus Nephritis?

A

Wire loop

= subendothelial deposits that cause circumferential thickening of capillary wall

20
Q

What population of people are usually affected by Henoch-schonlein purpura?

21
Q

What are the symptoms in children with Henoch-Schonlein Purpura?

A

Purpura of the legs, arms, butt
Abdominal pain and GI bleed
Athralgias and renal abnormalities

22
Q

What are the symptoms in children with Henoch-Schonlein Purpura?

A

Purpura of the legs, arm, butt
Abdominal pain with GI bleed
Athralgias and renal abnormalities

23
Q

If Henoch-schonlein purpura presents in adults, what symptoms will be more severe?

A

Renal symptoms

24
Q

With Henoch-Schonlein purpura, what does the child of a background of and a history of?

A

Background of atopy

History of recent URI

25
What is hallmark of Henoch-Schonlein purpuar?
IgA deposits in Mesangium
26
IgA deposits in the mesangium could indicate what 2 immune complex deposition diseases?
Henoch-Schonlein Purpura | IgA Nephropathy
27
IgA nephropathy is the most common cause of Nephritic syndrome/RPGN. Where will IgA be deposited?
Mesangium
28
What is a recurrent symptom of IgA Nephropathy?
Recurrent hematuria
29
What types of diseases can IgA nephropathy present with?
Celiac disease Liver disease Abnormal IgA synthesis
30
Besides IgA deposits in the mesangium with IgA nephropathy, what else will be deposited?
C3 | Properdin
31
What is a Pauci-Immune cause of Nephritic Syndrome/RPGN?
Granulomatosis with Polyangiitis
32
What marker will be (+) with Granulomatosis with Polyangiitis?
PR3 - ANCA
33
What usually causes Granulomatosis with Polyangiitis?
T cell hypersensitivity to an inhaled antigen
34
What are the general symptoms of Granulomatosis with Polyangiitis?
Granulomas and vasculitis of the respiratory tract
35
What is RPGN?
Rapid loss of renal function - -> oliguria and signs of nephritic syndrome - -> renal failure