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Year 3
SPINE
Renal Pathology
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Created by
Jessica Jardine
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Cards (16)
Fill in the blanks
A)
mesangial cells
B)
bowmans capsule
C)
afferent arteriole
D)
capillary loop
4
Fill in the blanks
A)
endothelium
B)
glomerular basement membrane
C)
podocyte foot processes
3
Minimal change disease - under microscope
Effacement/fusion of
podocyte
foot processes
Membranous nephropathy - under microscope
Immune complex deposits
(
subepithelial
)
Appearance of
spikes
Focal segmental glomerulosclerosis - under microscope
Primary disorder of
podocytes
scarring
of some
glomeruli
and
fusion
of
foot processes
Diabetic nephropathy - under microscope
Initial ->
diffuse glomerulosclerosis
(
increased mesangial matrix
)
Later ->
nodule formation
(
Kimmelstiel-Wilson lesion
)
Amyloidosis
Extracellular deposition
of
protein fibrils
with a characteristic
beta-pleated sheet
conformation
Under microscope ->
pale pink deposits
of
amyloids
within
glomeruli
,
Congo Red Stain
Nephrotic
Syndrome
Nephritic syndrome
Haematuria (RBCs &
red cell casts
)
Proteinuria (usually subnephrotic range) -> with or without oedema (ACR
< 300
mgm/mmol)
Uraemia
HTN
Does stage 5 SLE cause nephrotic or nephritic syndrome?
Nephrotic
Nephritic Syndrome causes
Immune-mediated
GN
IgA nephropathy
SLE
Post-infectious
Membranoproliferative glomerulonephritis
Pauci-immune
GN
ANCA associated microscopic vasculitis
Anti-GBM
disease
Most common cause of glomerulonephritis
IgA nephropathy
What is shown in the image?
Red cell casts
What is rapidly progressive glomerulonephritis?
Clinical syndrome
Rapid deterioration
in
renal function
Severe oliguria
& signs of
nephritic syndrome
If untreated ->
death
from
renal failure
within wks to
months
Under microscope ->
crescentic glomerulonephritis
What is shown in the image?
Crescentic glomerulonephritis
Anti-GBM disease
Autoimmune disease
Antibodies against
alpha-3
change of
type 4 collagen
in the
GBM
(
basement membrane
of
glomeruli
&
lung
)