updated GN Flashcards

1
Q

How do you differentiate between glomerulonephritis-associated hematuria and other causes of hematuria?

A

GN hematuria is associated with an abnormally shaped RBC
normal morphology in non-GN hematuria

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2
Q

What are the different presentations associated with glomerular disease?

A

asymptomaticc proteinuria
asymmptommatic hematuria
nephrotic syndrome
nephritic syndrome
RPGN
chronic GN

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3
Q

What type of injury is associated with nephritic vs. nephrotic?

A

nephrotic is associated with podocyte injury
nephritic is associated with sub-endothelial cell injury and GBM injury

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4
Q

What is characteristically found in RPGN?

A

crescent formation

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5
Q

what is the difference in urinary protein levels between nephritic and nephrotic ?

A

more than 3.5g in nephrotic
less than 3g in nephritic

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6
Q

what are the associated presentations/complications of nephrotic syndrome ?

A

hyperlipidemia
lipiduria
negative nitrogen balance ( muscle wasting )
hypercoagulability
infection
AKI

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7
Q

when are oval fat bodies found in the urine ?

A

in nephrotic syndrome

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8
Q

what type of AKI is associated with nephrotic ?

A

pre renal or ATN

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9
Q

what are the diseases that fall under nephrotic syndrome ?

A

MAD MF
Minimal change disease
Amyloidosis
Diabetic nephropathy
Membranous nephropathy
Focal segmental glomerulosclerosis

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10
Q

what are the diseases associated with nephritic syndrome ?

A

1- Acute diffuse proliferative GN :
acute post strept GN
lupus proliferative GN

2- IgA nephropathy
3- Alport Syndrome

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11
Q

which disease may present with both nephritic and nephrotic ?

A

membranoproliferative GN

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12
Q

what are the diseases associated with RPGN ?

A

Type 1 - good pastures syndrome
Type 2 - immune complex mediated GN
Type 3 - ANCA associated vasclitis

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13
Q

what is the other name for good pastures disease ?

A

anti glomerular basement membrane disease

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14
Q

what are the general supportive measures for each of these symptoms :
hypoproteinemia
proteinuria
edema
hypertension
hyperlipidemia
hypercoagulability
infection

A

hypoproteinemia - adequate protein intake

proteinuria - ACE or ARB

edema - loop diuretics and thiazide diuretics

hypertension- dietary salt restriction

hyperlipidemia - statins ezetimibe

hypercoagulability - prophylactic anticoag

infection - parental ab

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15
Q

what is the target blood pressure in patients with glomerular disease ?

A

below 130/80

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16
Q

what is the cause of post streptococcal GN ?

A

a type of acute nephritis
due to group A beta hemolytic streptococcal infection of the pharynx or the skin

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17
Q

which part of the glomeruli is affected in post streptococcal GN ?

A

subendothelial cells hence the hematuria

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18
Q

what is the presentation of acute post streptococcal GN ?

A

nephritic syndrome 1-4 weeks after a throat or skin streptococcal infection
usually occcurs in childhood

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19
Q

what is the specific investigation for post strep GN ?

A

ASOT ( anti streptolysin )

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20
Q

what is the treatment for post strep GN ?

A

general supportive treatment
if there is an ongoing infection give ab

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21
Q

what are the specific investigations associated with systemic lupus GN ?

A

anti dsDNA
anti smith
ANA

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22
Q

what is the treatment for SLE GN ?

A

immunosuppressive treatment

23
Q

what is the presentation of IgA nephropathy ?

A

recurrrent attacks of nephritic syndrome or macroscopicc hematuria 1-2 days after an URT or GIT infection

24
Q

what disease is associated with IgA nephropathy ?

A

celiac disease

25
what is the specific investigation associated with IgA nephropathy ?
elevated serum IgA
26
what is the treatment for IggA nephropathy ?
supportive + immunosuppressive and ab if there is an ongoing infection
27
what is the cause of alport syndrome ?
x linked hereditary glomerular disease
28
what type of collagen is deficient in alports syndrome ?
type 4
29
what is the clinical presentation of alports syndrome ?
nephritic syndrome recurrent attacks of macroscopic hematuria sensorineural deafness ocular abnormalities
30
what is the presentation of minimal change disease ?
nephrotic syndrome more common in children
31
what is the treatment of minimal change disease ?
1ry : corticosteroids 2ry : treat the cause
32
what are the different causes associated with secondary FSGS ?
HIV heroin Obesity
33
what is thee presentation of membranoproliferative GN ?
mixed nephritic and nephrotic
34
what is the other namme for goood pastures disease ?
type 1 RPGN or Anti GBM membrane
35
what is the clinical presentation associated with Goodpasture's disease ?
pulmonary hge and hemoptysis
36
what are the specificc antibodies associated with anti-GBM ?
anti GBM antibodies
37
what is the treatment for goodpasteurs disease ?
immunosuppressive agents plasma exchange
38
what is the prognosis of acute poost streptococcal GN ?
self limmitng associated with full renal recovery
39
what is thee prrognosis of minimal change disease ?
corticosteroids are usually useful in inducing remission but relapse is common
40
what is the prognosis of alports syndrome ?
almost all cases prrogress to CCKD
41
what is the prognosis of FSGS ?
almost all cases progress to CKD
42
what is the prognosis of membranous nephropathy ?
1- 25% of cases are resistant to therapy and progress to CKD 2- 75% of cases enter remission
43
what is the prognosis of lupus diffuse proliferative GN ?
outcomes are variable it depends
44
what are the glomerular diseases associated with SLE ?
1- acute proliferative GN 2- membranous nephropathy 3- MPGN
45
what are the glomerular diseases associated with HBV ?
membranous nephropathy MPGN
46
what aree the glomerular diseases associated with HCV ?
membranous nephropathy MPGN
47
what are the glomerular diseases associated with HIV ?
membranous nephropathy FSGS
48
what are the glomerular diseases associated with malignancy ?
membranous nephropathy
49
what are the systemic diseases associated with minimal change disease ?
respiratory tract infection Atopy Hodgkin's disease
50
what are the drugs associated with causing secondary gloomerrular disease ?
NSAIDs immunizations Penicillamine Pamidronate Interferon Heroin
51
how can you differentiate between acute post streptococcal GN vs IgA nephropathy ?
post strep happens 1-4 weeks after a throat or skin infection whilst IgA nephropathy happens 1-2 days after an URT or GIT infection
52
what are the diseases associated with membranoproliferative ?
HIV HCV HBV SLE plasma cell dyscrasias
53
what is the prognosis of membranoproliferative ?
50% progress to CKD
54
what is the prognosis of RPGN ?
renal function is rapidly lost