Glomerulopathies Flashcards

1
Q

ultrafiltrate

A

not urine yet but it’s the fluid that is generated in these structures

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2
Q

blood flow through kidney

A
  • Very high blood flow through the kidney

* Vasculature is very rich and could be important for pathophys

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3
Q

glomerulpathy

A

pathology related to the glomerulus (Preferred term to use b/c more open than glomerulonephritis)

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4
Q

Glomerulonephritis

A

inflammatory response

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5
Q

types of glomerulopathies

A

• Primary= disease which affects glomerulus first
• Secondary= other systemic diseases that affect glomerulus
○ Ex. SLE= autoimmune
○ Ex. Diabetes= affects primary glomeruli but can also affect other structures

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6
Q

what is one of the most common causes of chronic kidney disease?

A

chronic glomerulonephritis

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7
Q

types of primary glomerulopathies

A

• Acute= lasts few weeks
○ Not really serious consequences
○ Could be caused from infection
• Chronic= always leads to end stage renal disease (ESRD)
○ ESRD= chronic renal failure/ significant insufficiency in kidney function
○ Acute have high potential to progress to chronic
• Crescentic (rapidly progressive)= clinical course is quite fast; may lead to acute kidney failure
• Membranous glomerulopathy= basement memb is affected
•minimal-change disease
•focal-segmental glomerulosclerosis
•IgA nephropathy

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8
Q

systemic diseases with glomerular involvement

A

systemic lupus erythematosus (SLE) and DM

amyloidosis

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9
Q

Bowman’s space

A

surrounded by capillaries

When the filtrate is produced, it accumulates in the bowman space

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10
Q

Bowman’s capsule

A

covered by epithelial cells called parietal layer

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11
Q

filtrate coming into the glomerulus

A

when filtrate comes in, it has to pass through endothelium, basement membrane, and visceral layer of epithelial cells

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12
Q

hematouria

A

presence of RBCs in the urine

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13
Q

where does ultra-filtration occur at?

A

Space b/w podocytes

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14
Q

Which mechanism is most commonly in the pathogenesis of glomerulonephritis?

A

ANTIBODY-MEDIATED INJURY

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15
Q

antibody-mediated injury

A
  • Antibody together with target (immune complex) can deposit in glomerular structures and cause probs
  • Circulating immune complexes= formed somewhere else and get deposited in the kidney
  • Cytotoxic antibodies= go and kill certain cells but not common
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16
Q

activation of compliment in the kidney

A

can lead to cell lysis b/c of TCC (terminal complement complex)

17
Q

what is the best way to diagnose antibody-mediated injury?

A

kidney biopsy
○ Use antibodies to detect immune complexes
○ Important b/c sometimes treatment for glomerular nephritis is very harsh

18
Q

effacement

A

podocytes are becoming flat

Barriers are becoming very leaky and have cells going into the urine

19
Q

C5a

A

very potent inflammatory mediators → causes inflammation and recruits other immune cells to site of injury

20
Q

C5b-9

A

part of complement

bunch of proteins together

21
Q

symptoms of nephritic syndrome

A

HEMATURIA
azotemia (increases in blood nitrogen)
oliguria ( decreased amt of urine produced in 24 hours)
variable proteinuria (but mild), edema, HTN

22
Q

what is the normal amt of urine prod in 24 hours?

A

○ Normal= 1.5 L/day

○ Oliguria= <400 mL/day

23
Q

symptoms of nephrotic syndrome

A

PROTEINURIA >3,5 g/day
hypoalbuminemia
hyperlipidemia, lipiduria, edema

24
Q

symptoms of rapidly progressive glomerulonephritis

A

acute nephritis (like nephritic syndrome), proteinuria, acute renal failure

25
Q

symptoms of chronic renal failure

A

asotemia progressing to uremia

26
Q

what is the most common primary glomerular disease that causes nephritic syndrome?

A

acute proliferative (poststreptococcal-postinfectious) glomerulonephritis

27
Q

what is the most common systemic disease that causes nephritic syndrome?

A

SLE

28
Q

what are the two most common causes of nephritic syndrome?

A

primary glomerular diseases and systemic diseases

29
Q

minimal-change disease

A

most common in children