updated glomerulonephritis Flashcards

1
Q

in hematuria associated with glomerulonephritis what is special about the RBCs ?

A

abnormal shape and can show acanthocytes ( RBC budding) due to gglomerular cause

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2
Q

what is seen on macroscopic examination of urine that indicated proteinuria ?

A

frothy urine

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3
Q

if there is injury to the podocytes what is the presentation ?

A

proteinuria ( nephrotic )

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4
Q

if there is injury to the mesangial or endothelial cells what is the presentation ?

A

hematuria - nephritic

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5
Q

if there are breaks in the GBMM what is the presentation ?

A

hematuria - neephritic

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6
Q

what are the glomerular diseases generally divided into ?

A

asymptomatic proteinuria
asymptomatic hematuria
nephritic syndrome
nephrotic syndrome
macroscopic hematuria
rapidly progressive glomerulonephritis
chronic glomerulonephritis

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7
Q

what are the different etiologies for glomerular injury ?

A

antigen antibody complex
complement activation
t-lymphocytes
genetics

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8
Q

what is the difference between nephritic and nephrotic syndrome ?

A

nephritis - associated with hematuria, mild proteinuria
nephrotic - proteinuria above 3.5 mg/dl , hypoalbuminemia , oedema and ascites

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9
Q

hypertension is associated with nephritic or nephrotic ?

A

nephritic more commonly

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10
Q

what are the main characteristics of nephrotic syndrome ?

A

proteinuria above 3.5 mg/dll
hyperlipidemia
lipiduria
hypercoagulability - due. to loss of anticoagulants
ascites
generalized oedema - ascites , pleural effusion

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11
Q

how can nephrotic syndrome cause acute kidney injury ?

A

1- drugs that are used to treat nephrotic can cause AKI
2- renal vein thrombosis
3- no osmotic pressure due to lack of albumin, which causes pre renal AK if left for too long can cause ATN

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12
Q

what is rapidly progressive glomerulonephritis ?

A

similar to nephritic but kidney function loss happens over a week

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13
Q

what is the treatment for glomerular disease from a general supportive aspect ?

A

adequate dietary protein intake
ACE inhibitors or ARBS
loop diuretics
dietary sodium restriction

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14
Q

what is the goal for blood pressure in patients with glomerular disease ?

A

below 130/80

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15
Q

what is rapidly progressive glomerulonephritis characterized by ?

A

formation of crescents and hematuria with red cell casts ( which is also seen in nephritic)

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16
Q

what are the diseases that fall under the band off nephrotic syndrome ?

A

minimal change disease
focal segmental glomerulosclerosis
membranous nephropathy
amyloidosis
diabeticc nephropathy

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17
Q

what are the diseases that fall under the band off nephritic syndrome ?

A

acute diffuse proliferative glomerulonephritis ( Acute post-streptococcal glomerulonephritis
Lupus proliferative glomerulonephritis )
IgA nephropathy
Alport syndrome

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18
Q

what are the types of rapidly progressive glomerulonephritis ?

A

type 1 : goodpasture syndrome
type 2 : immune complex mediated glomerulonephritis
type 3: ANCA associated vasculitis

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19
Q

what disease falls under mixed nephritic and nephrotic syndrome ?

A

membranoproliferative glomerulonephritis

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20
Q

what is the cause of post streptococcal glomerulonephritis ?

A

chest or skin infection ( group b hemolytic streptococcal infection ) , affecting the sub epithelials area

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21
Q

what is the clinical presentation for acute post streptococcal GN ?

A

nephritic syndrome which present 1-4 weeks after a streptococcal infection ( sore throat or skin infection )

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22
Q

what age group is commonly associated with post strep GN ?

A

young children

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23
Q

what are the specific investigations for post strep GN ?

A

antistreptolysin O titre
ASOT

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24
Q

what is the clinical presentation of SLE proliferative GN ?

A

if the patient presents with :
nephrotic - membranous nephropathy
nephritic - lupus proliferative GN
mixed - MPGN

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25
what are the specific investigations for SLE proliferative GN ?
detection of autoantibodies : anti-dsDNA Anti-smith ANA
26
what is the cause of IgA nephropathy ?
after a respiratory tract or GIT infection abnormal Ig formation occurs which then acts as the antigen
27
what is the CP of IgA nephropathy ?
recurrent attacks of nephritic syndrome or macroscopic haematuria 1-2 days after thee infection and usually occurs in older patients
28
what disease is IgA nephropathy associated with ?
Celiac disease
29
what is the specific investigation for IgA nephropathy ?
elevated serum IgA
30
what is the cause of Alports syndrome ?
x linked hereditary disease mutation in type 4 collagen of the basement membrane
31
what is the clinical picture of alports syndrome ?
nephritic syndrome recurrent attacks of macroscopic hematuria sensorineural deafness ocular abnormalities
32
what are the different causes of minimal change disease ?
primary : abnormal T lymphocyte activity secondary : respiratory tract infections atopy immunizations hodgkin's lymphoma NSAID therapy in adults
33
what is the clinical presentation of MCD ?
nephrotic syndrome , and primary is more commonly seen in children
34
what is thee treatment for 1ry and 2ry MCD ?
1ry MCD : immunosuppressive drugs , first line corticosteroids 2rry MCD : treat the cause - no immunosuppressive
35
what is the cause of primary focal segmental glomerulosclerosis ?
abnormal T lymphocyte activation may also be hereditary
36
what are the causes of secondary FSGS ?
HIV Heroin pamidronate - drugs for osteoporosis interferon
37
what is the effect of circulating permeability factors ?
damage to the podocytes , causing effacement and hence nephrotic syndrome
38
what are the causes of primary membranous nephropathy ?
immune complex formation
39
what are the causes of secondary membranous nephropathy ?
malignancy HBV , HCV , HIV SLEE drugs : NSAIDs, penicillamine
40
what is the clinical picture of membranous nephropathy ?
nephrotic syndrome
41
what is different about the presentation of membranoproliferative GN ?
present with nephrotic and nephritic proteinuria of more than 3.5 , edeema, hematuria and hypertension
42
what are the secondary causes of secondary membranoproliferative GN ?
HCV, HBV SLE plasma cell dyscrasias - like multiple myelomas
43
what is the cause of goodpasture disease ?
auto antibodies against alpha 3 chain of type 4 collagen off thee GBM and alveolus BM
44
what is the clinical presentation of goodpasture syndrome ?
rapidly progressive GN ( crescent formation ) pulmonary hge and hemoptysis
45
what is the other name for good pasture's disease ?
anti GBM disease
46
what is the treatment for good pastures disease ?
immunosuppressive and plasma exchange
47
what is the specific investigation for goodpasture's disease ?
anti-GBM antibodies
48
what are the three different types of RPGN ?
type I : good pasture type II : immune complex mediated GN type III : ANCA associated vasculitis
49
what is the prognosis for acute post strep GN ?
self-limiting , associated with full renal recovery
50
what is the prognosis of minimal change disease ?
corticosteroids are effective in remission relapse is common
51
what is the prognosis for alport and FSGS ?
almost all cases progress to chronic kidney failure
52
what is the prognosis of RPGN ?
renal function deteriorates rapidly and is often irreversible
53
what is the prognosis for IgA and MPGN ?
50% will progress to CKD over time
54
what is the prognosis for membranous nephropathy ?
25% of cases are resistant to therapy and progress to CKD 75 % off cases enter remission
55
what is the prognosis of lupus diffuse proliferative GN ?
outcomes are variable
56
generally do nephrotoxic drugs cause nephritic or nephrotic ?
nephrotic
57
what is the difference between acute post strep glomerulonephritis and IgA nephropathy ?
post strep - presents with nephritic present 1-4 weeks after infection of the skin or throat and usually occurs in children IgA nephropathy - recurrent attacks of nephritic syndrome or macroscopic hematuria presents 1-2 days after GIT or resp tract infection and is seen in older patients
58
what is the treatment for post strep GN ?
treat with antibiotics
59
what specific investigation can be ordered for a patient with alports ?
genetic testing
60
Is there any role for testing or investigating other family members? If yes, what investigations would you request for patients with alport's ?
family members should be screened for hematuria
61
what is the most common nephrotic disease in children ?
minimal change nephropathy
62
why are patients with nephrotic syndrome more prone for thromboembolic events ?
* Risk of thromboembolic events due to decreased levels of natural anticoagulants (due to urinary losses) such as: a. anti-thrombin III b. Plasminogen c. protein C and S * Avoid thromboembolic events by using prophylactic anticoagulation with heparin, warfarin.