Acute nephritis, glomerulonephritis and acute tubular necrosis Flashcards

1
Q

Nephritic syndrome definition

A

Characterised by:
- Haematuria
- Proteinuria
- Leucosuria

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2
Q

Acute interstitial nephritis
- Description
- Causes

A

Inflammation of the renal interstitium (between renal tubules)
- Commonly caused by hypersensitivity to medication

Causes:
- Drug allergy: antibiotics (beta-lactam, fluroquinolones)
- PPIs
- NSAIDs
- Chemo
- AI/ inflammatory disease: Sjorgren, TINU, sarcoid
- Infective: staph, strep, Brucella.

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3
Q

Acute interstitial nephritis
- Presentation

A

Mild renal impairment
- Poor renal function= worse prognosis

If drug reaction, allergy picture
- Rash, fever, peripheral eosinophilia.

Oedema
- if NSAIDs used, presents with nephrotic syndrome

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4
Q

Investigations for acute interstitial nephritis

A

Definite diagnosis= biopsy
- Inflammatory cell infiltrate in interstitium

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5
Q

Nephritic causes of glomerulonephritis

A

IgA nephropathy

Post-infectious GN

Rapidly progressive GN

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6
Q

Rapidly progressive GN
- Description
- Causes

A

Characterised by rapid decrease in eGFR

Causes
- Type 3: ANCA related vasculitis: granulomatosis with polyangitis (Wegner’s), microscopic polyangiitis

  • Type 1: anti-GBM autoantibodies= Goodpasture syndrome,

Type 2: Immune complex deposition: SLE, IgA nephropathy

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7
Q

Treatment of Rapidly progressive GN

A

Rituximab

Corticosteroids

Cyclophosohamide
- azathioprine

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8
Q

Post-infectious GN
- Description
- Histology
- Causes

A

Type 3 hypersensitivity reaction
- Antibodies bind to sites on glomerulus and activates complement

Histology
- Proliferative GN: proliferation of endothelium and mesangium.

Causes
- Streptococcal infection (weeks post-infection)

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9
Q

Pathophysiology of acute tubular necrosis

A

Ischaemia or nephrotoxic injury to the renal tubules leading to death of tubular endothelial cells.

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10
Q

Acute tubular necrosis causes

A

Reduced perfusion
- Dehydration
- Circulatory shock
- Massive haemorrhage

Nephrotoxins
- Aminoglycoside antibiotics
- Contrast dye
- Rhabdomyolysis

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11
Q

The most common pathological cause of an AKI is…

A

Acute tubular necrosis

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12
Q

State the phases of acute tubular necrosis

A

Oliguria/anuric phase
- Damage to tubular cells= less filtration and urine production

Polyuric phase
- Tubular cells are regenerated, leading to increased urine production

Recovery phase
- Urine output returns back to baseline

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13
Q

Urinalysis findings for acute tubular necrosis

A

“Muddy brown casts”

Proteinuria

Urine osmolality <350

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14
Q

Histopathological findings of acute tubular necrosis

A

Necrotic, epithelial tubular cells
- loss of nuceli

Detached tubular cells

Dilated tubules

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15
Q

Chronic interstitial nephritis is most commonly caused by…

A

Prolonged use of NSAIDs

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16
Q

Urine studies findings for interstitial nephritis

A

May show eosinophilia in hypersensitivity reaction

White cell casts

Proteinuria, haematuria

17
Q

Kidney ultrasound in interstitial nephritis will show…

A

Increased cortical echogenicity

18
Q

IgA nephropathy is also known as…

A

Berger’s disease

19
Q

Causes/ associations of IgA nephropathy

A

Upper respiratory tract infection
- Typically occurs within days

Coeliac disease

HIV

Alcoholic liver disease

20
Q

IgA nephropathy presentation

A

Nephritic syndrome

Macroscopic haematuria

AKI

21
Q

Nephrotic syndrome causes of glomerulonephritis

A
  • Minimal change disease
  • Focal segmental glomerulosclerosis
  • Membraneous GN
  • Membranoproliferative GN
22
Q

Nephritic syndrome causes of glomerulonephritis

A

Mesangial proliferative/ IgA nephropathy

Post-infectious/ diffuse proliferative GN

Rapidly progressive/ crescentic GN

23
Q

Focal segmental glomerulosclerosis (FSGS) pathology

A

Segmental glomerular scarring and podocyte damage.

24
Q

Renal biopsy in minimal change disease will show

A

Loss of podocyte processes/ fusion of podocytes

25
Q

What treatment is effective in most cases of minimal change disease?

A

High dose prednisolone

26
Q

Management of post-infectious GN

A

Typically self-limiting disease so management is supportive

27
Q

Renal histology findings in membranous GN

A

Immunofluorescence
- Granular IgG deposits
- C3 deposits