Renal Flashcards

1
Q

what is mode of inheritance of PKD

A

AD or AR

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2
Q

what is presentation of PKD

A

HTN, flank pain, haematuria

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3
Q

what other risk occurs with PKD

A

risk of BERRY NEURYSM

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4
Q

what is acute renal failure

A

RAPID deterioration in renal funvion

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5
Q

what are causes of. AKI

A

pre renal: failure of perfusion
renal: acute tubular injury, acute glomerulomnephritis, thrombotic micrpoangiopathy
post-renal: obstruction

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6
Q

what is the msot common cause of AKI

A

acute tubular injury

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7
Q

what can cause tubular injury

A

ischaemia
toxins
drugs

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8
Q

what is acute glomerulonephritis q

A

acute inflammaation of the glomeruli

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9
Q

what is the KEY HISTO feature of acute glomerulonephritis

A

CRESCENTS on microscopu

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10
Q

what are causes of acute glomerulonephritis

A

immune complex deposition (IgA)
anti-GBM disease (goodpastures)
Pauci-immune

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11
Q

what is another name of goodpastures disease

A

anti-GBM

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12
Q

what occurs in goodpastures

A

antibodies against C terminal domain of T4 collages

may clross react wiuth albeolar basement membrane, causing pulmonary haemorrhage

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13
Q

what does immunohisto for goodpastures show

A

linear deposition of IgG on glomerular basement membrane

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14
Q

what is thrombotic microangiopathy

A

damaage to endothelium ion glomeruli/arterioles > lead to thrombosis e.g. MAHA, HUS

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15
Q

list causes of nephrotic syndrome

A

minimal change disease
focal segmental glomerulosclerosdis
membramous glomerulonephritis

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16
Q

what occurs histologically in minimal change disease

A

loss of podocytes

17
Q

what occurs histologically in membramous glomerulonephritis

A

thickening of GBM

18
Q

what nodules are pathomnemonic of diabetic nephropathy

A

Kimmelsein-Wilson nodules (stage 3)

19
Q

what is AA amyloidosis associated with

A

chronic inflamm condition

20
Q

What is AL amyloid associated with

A

Ig light chains, so multiple myeloma

21
Q

explain clinical presentation of Alport syndrome

A

X linked dominant

deafness, ocular disease

22
Q

3 primary causes of nephrotic syndrome

A
  1. Minimal change disease
  2. Membranous glomerulonephritis
  3. Focal Segmental glomerulosclerosis
23
Q

Who does minimal change disease occur in

24
Q

What is seen on electron microscopy in Minimal change

A

loss of podocytes

25
WEhat is seen on microscopy of membranous glomerulonephritis
loss of podocytes, spiky subendothelial deposits
26
What is seen on microscopy of Focal Segmental glomerulosclerosis
Focal and segmental glomerulosclerosis and scarring | hyalinosis
27
Give two secondary causes of nephrotic syndrome
Diabetes | Amyllidosis
28
What is seen on histology of nephrotic syndrome with diabetes
Thickened Basement membrane | Kimmelstein wilson nodules aka mesangial matrix
29
list 5 causes of NEPHRITIC syndorme
1. Post strep GN 2. IgA nephropathy (Berger Disease) 3. Crescentic (rapidly rogressive) GN 4. Alport's (hreditary nephritis) 5. Benign familial haematuria (thin basement membrane disease)
30
Explain Alport syndrome
X linked mutation in T4 collagen Nephritic syndrome + sensorineural deafness + eye disorder
31
Explain Benign Familial Haematuria (thin basement membrane disease)
AD mutation for T4 collagen Causes diffuse thinnning of GBM Usually asymptomatic
32
What are the three key causes of asymptomatic haematuria
Thin basememnt membrane diseas e IgA nephropathy Alport
33
How does nephritic syndrome cause HTN
inflammation of glomerular vessels allowing red blood cells to enter the renal tubule; as they enter they are damaged. The body compensates for inflammation by slowing renal blood flow this causes oliguria > water retention >hypertension.
34
what is the timeline for IgA nephropathy after infection
only 1-4 days post resp/GI infectioN!!