glomerulonephritis Flashcards

1
Q

• terms used to describe histologically the number of glomeruli affected in a given condition:

A

diffuse: majority of glomeruli abnormal (>50%)
focal: some glomeruli affected

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2
Q

terms used to describe histologically the extent to which individual glomeruli are affected in a given condition:

A

ƒ global: entire glomerulus abnormal

ƒ segmental: only part of the glomerulus abnormal

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3
Q

proliferation

A

hyperplasia of one of the glomerular cell types (mesangial, endothelial, parietal epithelial), +/- inflammatory cell infiltration

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4
Q

membranous changes

A

capillary wall thickening due to immune deposits or alterations in basement membrane

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5
Q

crescent formation

A

parietal epithelial cell proliferation and mononuclear cell infiltration form crescent-shape in Bowman’s space

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6
Q

gold standard to assess degree of proteinuria

A

24-h urine protein

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7
Q

microalbuminuria defn

A

ACR ≥2.8 mg/mmol (female) or ≥2.0 mg/mmol (male)

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8
Q

screen for diabetic nephropathy

A

urine ACR

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9
Q

normal daily excretion of protein

A

<30g albumin

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10
Q

microalbuminuria, proteinuria, nephrotic syndrome

A

30-300mg albumin, 300mg-3g protein, >3.5g protein with hypoalbuminaemia (<35g/L)

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11
Q

ix for nephrotic syndrome or nephritic syndrome

A
Nephrotic:
Urinalysis
FBE, UEC, LFT, CRP/ESR
Glucose
Serology: ANA, RF, p-ANCA, c-ANCA, HBV, HCV, HIV, ASOT
Immunoglobulins
Urine MCS, 24h urinary protein and creatinine
Renal ultrasound

Nephritic is same, but add 24h urine stone workup if there is a history of stone formation

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12
Q

indications for nephrology referral

A

heavy proteinuria (ACR >30mg/mmol) or nephrotic syndrome

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13
Q

broad categories of proteinuria

A

tubulointerstitial, glomerular, overflow

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14
Q

tubulointerstitial proteinuria

A

impaired resorption

s syndrome

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15
Q

glomerular proteinuria categories

A

primary, secondary

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16
Q

primary glomerular proteinuria

A

minimal change, membranous, FSGS, membrano-proliferative, post-strep, IgA

17
Q

secondary glomerular proteinuria categories

A
systemic disease
hereditary/metabolic
infectious
medications
cancer
others
18
Q

secondary glomerular proteinuria systemic disease

A

diabetes, SLE, vasculitis

19
Q

hereditary/metabolic

A

Alford’s, PCKD, Fabry’s, SCD

20
Q

infectious

A

HBV, HCV, HIV, bacterial endocarditis

21
Q

medications

A

NSAIDs, gold, heavy metals

22
Q

cancer

A

lymphoma, RCC

23
Q

others

A

cryoglobulinaemia, hypertensive nephrosclerosis

24
Q

overflow proteinuria

A

overflow of low molecular weight proteins e.g. multiple myeloma, amyloidosis, Waldenstrom’s macroglobulinaemia

25
urine workup for gross haematuria
Centrifuge. If sediment red - true haematuria (RBC+, dipstick+) If supernatant red (RBC-) - dipstick for haeme If dipstick+, myoglobinuria or haemoglobinuria If dipstick-, pseudohaematuria (beetroot, rifampicin, porphyria)
26
primary nephritic syndrome causes
``` post-strep IgA rapidly progressive membrano-proliferative interstitial nephritis papillary necrosis ```
27
features of nephritic syndrome
``` PHAROH proteinuria haematuria azotemia RBC casts oliguria hypertension ```
28
acute nephritic syndrome defn
a subset of nephritic syndrome in which the clinical course proceeds over days
29
nephritic syndrome pathology types
1. Anti-GBM mediated (15%) 2. Immune complex mediated (24%) 3. Non-immune mediated (60%) 4. Double antibody positive
30
anti-GBM mediated pathology
anti-GBM positive. linear inflammatory pattern due to IgG and C3 deposition along the capillary loops.
31
anti-GBM ddx
with lung haemorrhage: goodpasture's | without lung haemorrhage: anti-GBM
32
type II pathology
granular pattern due to sub endothelial or subepithelial deposits of IgG and C3
33
type II ddx
C3 normal - IgA nephropathy, HSP | C3 decreased - post-strep, membrano-proliferative, SLE, IE, cryoglobulinaemia
34
type III pathology
pauci-immune. no immune staining. ANCA +ve
35
type III ddx
c-ANCA +: granulomatosis with polyangitis | p-ANCA +: microscopic polyangitis, churg-strauss
36
type IV pathology
features of type I and type III. double anti-body positive
37
lab features of RPGN
fibrous crescents on histopathology | RBC casts and/or dysmorphic RBCs in urine