GN Flashcards

(67 cards)

1
Q

The most common cause of chronic kidney injury.

A

glomerular disease

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2
Q

Should always be considered in the differential diagnosis when the urinary protein excretion is elevated or the urine sediment reveals RBCs.

A

glomerular disease

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3
Q

pathognomonic for glomerular disease.

A

Proteinuria (>3.5 g/d) or RBC casts in the urine sediment

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4
Q

Whats the definitive diagnosis of glomerular disease

A

renal biopsy

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5
Q

whats the type of collagen in the glomerular basement membrane

A

type 4

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6
Q

mutations in a345

A

alport syndrome

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7
Q

antibodies to NC1 domain of a3

A

goodpastures

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8
Q

GBM is

A

300nm

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9
Q

state the two immune mechanisms by which pathogenesis of glomerular disorders takes place

A

t cell i.e. MCD , antigen antibody dependent pathways

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10
Q

name two circulating immune complezes that get trapped in the glomeruli

A

sle, POSTSTREPTOCOCCAL

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11
Q

what are the systemic complications of nephron loss (4)

A

hyperlipidemia, hyperphosphatermia, systemic hypertension, hyperparathryoidism

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12
Q

name the adaptive changes that happen in remanant nephrons due to nephron loss

A

glomerular hypertension, proteinuria

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13
Q

name the 5 places where injury to the glomerulus could occur

A

visceral and parietal epi, mesangial , basement membrance, endothelium

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14
Q

injury to the endothelium manifests as ________________, give an example

A

hypercellularity i.e. acute poststreptococcal glomerulonephritis

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15
Q

acummulation of extracellular matrix manifests as injru to the _________________example__________

A

mesangium, diabetic nephropathy

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16
Q

give an example where thinning of the basement membrane with lamellation occurs

A

alport syndrome

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17
Q

thekening of the GBM

A

diabetic nephropathy

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18
Q

proliferation with crescent formation

A

parietal epithelium

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19
Q

detachment of podocytes igive an example

A

focal segmental glomerulosclerosis

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20
Q

foot process effacement

A

minimal change disease

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21
Q

moderate edema is in nephritic or nephrotic syndrome

A

nephritic

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22
Q

hematurica, oliguria, azotemia are all characteritstics of

A

nephritic syndrome

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23
Q

moderate proteiunuria is in nephritic or nephrotic s

A

nephritic

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24
Q

hypercoagulability, lipiduria, hyperlipidemia, hypoalbuminemia are characteristics off

A

nephrotic syndrome

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25
rapidly progressive renal failure with heamaturia w/ RBCs casts
RAPIDLY Progressive glomerulonephritis
26
what is the primary nephrotic syndrome that is the most in children 70%
minimal change disease
27
what is the primary nephrotic syndrome that is the most in adults 35%
focal segmental glomerulosclerosis
28
what is the primary nephrotic syndrome that presents as 30% in adults
membranous nephropathy
29
T or F, minimal change disease prognosis is bad
false, its excellent
30
state secondary causes of minimal change disease
NSAIDs, Hodgkins disease, viral
31
focal segmental glomerulosclerosis is more prevalent among
african americans and hispanics
32
how many cases of FSGsclerosis progress to ESRD
>50%
33
mutations involving vairous slit diaphragm proteins is a hereditary form of
FSGS
34
rule of third applies to which nephropathy?
membranous nephropathy
35
gold and penicillamine can ppt which type of nephropathy?
membranous nephropathy
36
HBV and HCV, syphilis, schistosomiasis, and malaria can ppt which type of glomerular disease
membranous nephropathy
37
state the five causes of membranous nephropathy
drugs, infections, carcionma, autoimmune disorders, idiopathic
38
state another name for membranoproliferative glomerulonephritis
mesangiocapillary glomerulonephritis
39
what is often almost always seen by analysing serum of mambranoproliferativenephritis
hypocomplementemia
40
membranousproliferative glomeruloneprhitis is associated odten with
HCV
41
which disease is both nephritic and nephrotic
membranoproliferative glomerulonephtitis
42
whats the leading cause of ESRD in many countries
diabetic nephropathy
43
what happens in the early stages of diabetic neprhopathy
hyperfileration and microalbuminuria
44
STRUCTURAL CHANGES (Increasing glomerular basement membrane thickening and mesangial expansion), which part of diabtic neprhopathy
preclinical (5y)
45
Hyperfiltration, microalbuminuria, rising blood pressure, which stage of diabetic nephropathy
incipent (15y)
46
before overt nepphropthay what appears in the urine?
proteinuria onset (20y)
47
Rising Scr, Decreasing GFR | , which part of diabetic nephropathy
oveert (10y)
48
whats beyond overt nerphpathy
end stage renal disease (30y)
49
multisystem involvement with poor prognosis
amyloidosis
50
male: female of SLE
1:10
51
Low C3 & positive Ab to ASO & DNAse B
ACUTE PROLIFERATIVE GLOMERULONEPRHITIS
52
THE MOST common cause of glomerulonephropathy isss
IgA neprhopathy aka Berger syndrome
53
describe the course of bergers syndrome
starts off as begnin and then ends with ESRS
54
Henoch-Schonlein purpira is a cause off
Bergers syndrome
55
crescentic GN or might present as simple
rapidly progressive glomerulonephritis
56
cellular cresents in RPGN is found in more than
50% of the glomeruli
57
if left untreated, RPGN _________
>90% progresses into ESRD
58
IgG deposit along GBM (anti-GBM disease)
Type 1 RPGN
59
IC deposition in the subendothelial, subepithelial, and/or mesangial compartment (virtually any IC–mediated GN, although most are idiopathic).
type 2 RPGN
60
absence of immune deposits “pauci- immune GN”. (ANCA vasculitis)
type 3 RPGN
61
Double-antibody positive disease is a unique variant of RPGN characterized by features of
type 1 and type 3 disease (i.e. anti-GBM antibodies and ANCA are both detected).
62
Typically presents with microscopic hematuria and mild proteinuria (<2.0 g/d) • May have: ocular abnormalities (retinopathy and anterior lenticonus), sensorineural hearing loss and rarely, leiomyomatosus.
alport syndrome
63
follows angiographic procedures by days or weeks
renal atheroembolic
64
renal atheroemboli is reported in _____of cases
30%
65
on biopsy, pts with renal atheroembloli have
atherosclerotic aorta, cholesterol emboli
66
blood chemistry of pts with renal artheroemboli
low complements, high esinophils
67
secondary to E. coli (serotype 0157:H7).
HUS