Nephritic Syndrome Flashcards

0
Q

What else does nephritic syndrome pResent with?

A

LAHHOR

Limited protein urea <3.5 g/day

Azotaemia

Hypertension = salt + fluid retention = oedema = at eyes as little bit of oedema that does occur particularly shows itself + loose connective tissue

Hyper cellular - neutrophils

Oliguria

RBC casts - glomerular bleeding + hematuria

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1
Q

What is the hallmark of nephritic syndrome?

A

Glomerular inflammation

Glomerulal bleeding

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2
Q

What is special about the strain that causes poststreptococcal glomerular nephritis?

Where does immune complex deposition start and how does it progress?

A

The nephritogenic strains = carry M protein virulence factor

IC start subendothelial – > Work their way up – >
pile of subepithelially – >
deposit into space + disappear

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3
Q

When and What do patients with poststreptococcal glomerular nephritis present with?

A

HSR3 2-3 wks after infection

Haematuria = cola colour urine
Hypertension,
oliguria,
periorbital oedema

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4
Q

For poststreptococcal glomerular nephritis what do we see on
light microscopy
immunofluorescence and
electronmicroscopy

A

@LM here = hypercellular + inflamed/enlarged glomerulus

@IF = granular IF

@EM = subepithelial hump

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5
Q

What’s the labeork for PSGN?

What is the treatment for Poststreptococcal glomerulal nephritis

A

⬆️anti-DNase B titers + ⬇️ complement levels

Csupportive

@Kids = rarely progressed renal failure
At adults develop renal failure = rapidly progressive glomerular nephritis

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6
Q

What does the biopsy in a rapidly progressive glomerulonephritis show?

A

@LM + IF =

Crescent moon shaped
|
|-> fibrins + plasma protein eg C3b
Macrophages +
Glomerulal parietal cells +
Monocytes

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7
Q

YOUNG ADULT Patient
presents with
LINEAR immunofluorescence , Haemoptysis, hematuria

What does he have and explain the IF

A

Goodpasture’s syndrome

Type 2HSR - anti-basement membrane antibody against basement membrane

Alveolar +
glomerular basement membrane = sharp line

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8
Q

In Lupus what is the most common cause of death?

A

Renal failure - diffuse proliferative glomerulonephritis

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9
Q

If a patient with lupus presents with a nephrotic syndrome which nephrotic syndrome will it be?

A

Membranous nephropathy

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10
Q

Patients has crescent moon shaped Glomerulitis With a GRANULAR immunofluorescence. What’s is the DDX?

A

Post strep glomerular nephritis

Diffuse proliferative glomerulonephritis i.e. deposits immunocomplex underneath endothelial cell = subendothelial = Lupus

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11
Q

Patient has crescent moon shaped glomerulitis

A negative immunofluorescence = PAUCI immune . What test needs to be performed after this

A

ANCA Anti neutrophil cytoplasmic antibody

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12
Q

patient has haemoptysis + haematuria + rapidly progressive glomerulal nephritis .Patient has crescent moon shaped glomerulitis. The patient has a history of sinus problems and has sinusitis. What’s does he have ?

A

Where can I granulomatosis.

It’s not Goodpasture because Goodpasture does not have naso pharynx problems

Patient would also have A negative immunofluorescence = PAUCI immune. Has a c-ANCA…..!!!!! Goodpasture has linear IF

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13
Q

patient has haemoptysis + haematuria + rapidly progressive glomerulal nephritis .Patient has crescent moon shaped glomerulitis. A negative immunofluorescence = PAUCI immune. Has a p-ANCA. What’s the DDX?

A

Microscopic polyangiitis doesn’t have the things mentioned below

Churg Strauss =
Asthma
granulomatous inflammation
eosinophilia

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14
Q

patient has haemoptysis + haematuria + rapidly progressive glomerulal nephritis .Patient has crescent moon shaped glomerulitis. A negative immunofluorescence = PAUCI immune. Has a p-ANCA. Patient has asthma, granulomatous information, eosinophilia. What is it

A

Churg Strauss

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15
Q

What is the most common at nephropathy worldwide

Explain how mucosa infection leads to IgA nephropathy

A

IgA nephropathy

Mucosal infection = produce XS IgA to defend against mucosal infection – >
some IgA goes to mesangium + deposit as immune complex –>
glomerular bleeding = episodic gross/microscopic hematuria

HENLOCH SCHONLEIN PURPURA

16
Q

In Ig a nephropathy where are the immunocomplexes deposited?

A

Mesangium of glomeruli

17
Q

A patient with a type 4 collagen issue comes in and says he cannot see, cannot pee, cannot hear a buzzing bee.
The electromicroscopy revealed a Basketweave appearance.

what problem does he have

A

Alport syndrome = thinning + splitting of basement membrane

18
Q

What causes diffuse proliferative glomerular nephritis?

A

SLE1 membranoproliferative glomerular nephritis

19
Q

What does light microscopy
Electromicroscopy
Immunofluorescence show

In diffuse proliferative glomerulonephritis?

A

LM = wire looping of capillaries

EM =
subendothelial +
intramembranous IgG IC’s +
C3 deposition

IF=granular

20
Q

What Diseases often present is nephrotic and nephritic syndrome concurrently?

A

Diffuse proliferative glomerular nephritis

Membranous proliferative glomerulonephritis

21
Q

Explain pathogenesis of Alport syndrome

A

Inherited type 4 collagen – >
thinning + splitting on BM – >

Isolated hematuria only
+
BM @ ears = damaged = sensory hearing loss
BM @ eye = damaged = ocular disturbance

22
Q

What does electron microscopy reveal for Alport syndrome

A

Basket weave appearance