Glomerulonephritis Flashcards

1
Q

Definition of glomerulonephritis

A

Inflammatory lesions of the glomerulus

Does not include:

  • Non-inflammatory lesions affecting the Glomerulus
  • Hypertension, diabetes, haematological malignancy
  • Rhabdomyolysis
  • AKI associated glomerulonephritis
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2
Q

Nephrotic syndrome definition

A

Preserved renal function

  • Characterised by proteinuria. (>3g/day)
  • Decreased serum albumin and total protein

Features

  • Oedema
  • UPCR> 300mg/mmol
  • ACR> 180mg/mmol
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3
Q

Nephritic syndrome definition

A

Impaired renal function characterised by:

  • Proteinuria
  • Haematouria
  • Leucosuria
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4
Q

Glomerulus anatomy

A

Blood enters the apparatus via the afferent arteriole and undergoes filtration through the glomerulus

Inner lining= endothelial cells
Middle layer= basement membrane
Outer layer=Epithelial foot processes (podocytes). Wraps around capillaries, leaving slits.

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5
Q

Histological categories for glomerular disease

A

Focal or diffuse

Segmental or global

Crescents

Minimal changes

Structures affected: Mesangium, basement membrane, epithelial comma and a video.

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6
Q

Symptoms of glomerulonephritis

A
  • Systemic, flulike symptoms
  • rash
  • arthralgia
  • swelling
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7
Q

Investigations into glomeurulonephritis

A

Urine analysis

Blood tests

  • Serum albumin and protein
  • Renal function tests
  • Autoimmune screen

Renal biopsy analysis

  • Light Microscopy
  • immunohistology
  • electron microscopy
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8
Q

Urine analysis results

  • Nephrotic syndrome
  • Nephritic syndrome
A

Nephrotic

  • Significant proteinuria
  • Blood and leucocytes may be present.
  • No nitrites

Nephritic

  • Haematuria
  • Proteinuria
  • Leucouria
  • No nitrites.
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9
Q

Causes of GN

A

Idiopathic

Infection: HBV, HCV, Strep, HIV

Autoimmune: SLE, Goodpasteurs, Vasculitis

Drugs: penicillamine, gold

Amyloidosis

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10
Q

Minimal change GN

  • Associations
  • Histology
A

Most common cause of nephrotic syndrome in children.

Associations

  • NSAIDs
  • Allergy
  • Lithium, gold
  • Hodgkin’s

Histology

  • Electron microscopy: fusion of podocytes, loss of foot processes
  • Appears normal in light microscopy.
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11
Q

Minimal change GN

  • Presentation
  • Treatment
A

Presentation

  • Nephrotic syndrome: oedema, hypoalbuminaemia, proteinuria
  • Frothy urine
  • Preserved renal function

Treatment

  • Steroids
  • Calcinuerin inhibitors, i.e tacrolimus.
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12
Q

Membranous GN

  • Associations
  • Histology
A

Cause of nephrotic syndrome in 20-30% adults.

Associations

  • Drugs: penicillamine, gold, captopril, mercury
  • Paraneoplastic: colon, breast, lung
  • Autoimmune: Sjorgen’s, SLE, RA, ank spondy
  • Idiopathic
  • Infection: Hep B, C

Histology
- Silver stain–> Sub-epithelial deposits of immune complex

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13
Q

Membranous GN

  • Presentation
  • Treatment
A

Presentation

  • Nephrotic syndrome
  • AKI
  • CKD

Treatment

  • Treat underlying cause
  • Steroids
  • Calcineurin inhibitors
  • Blood pressure control.
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14
Q

Mesangial proliferative GN

  • Pathology
  • Causes
  • Presentation
A

Mesangial proliferation and matrix desposits

  • Due to increased IgA
  • mesangial cells proliferate when IgA increases

Causes

  • Thyphoid
  • malaria
  • IgA nephropathy

Presentation

  • AKI
  • haematuria
  • CKD
  • Hypertensive crisis
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15
Q

Diffuse proliferative nephritis (DPN)

  • Pathology
  • Causes
  • Treatment
A

Commonly affects people with SLE

  • Endothelial and mesangial proliferation
  • Can show crescents filling Bowman’s space
  • IgM, IgG, C3 deposits.

Causes

  • Endocarditis
  • Post-strep GN

Treatment
- Treat underlying infection

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16
Q

Focal segmental glomerulosclerosis (FSGS)

  • Causes
  • Pathology
A

Primary= Idiopathic

Secondary causes:

  • Familial: after transplantation.
  • Viral infection: HIV
  • Drugs: Heroin, pamidronate.
  • Obesity
  • HTN
  • Atheroemboli
  • SCD

Pathology
- Segmental scarring of glomerulus.

17
Q

Rapidly progressing glomerulonephritis (Crescentic GN)

- Pathology

A

Anti-neutrophil cytoplasmic antibodies (ANCA) interact with antigens in neutrophil’s cytoplasm.
-Neutrophils release lytic enzymes, causing glomerular crescents containing parietal epithelial cells (Bowman’s capsule) and sometimes podocytes.

18
Q

Rapidly progressing glomerulonephritis (Crescentic GN)

- Associations

A

ANCA related small vessel vasculitis

  • Granulomatosis with polyangitis (GPA)
  • Microscopic polyangitis

Goodpastuer’s

Agressive IgA nephropathy
- As seen with SLE

Idiopathic

19
Q

Treatment for RPGn

A

Strict blood pressure control

ACEi if proteinuria >1g/day

Immunsuppresions

20
Q

Immunosuppressive drugs used for crescentic GN

A

Steroids

Cyclophosphamide

Azathiprine

Mycophenolate mofetil

Rituximab

21
Q

Membranoproliferative/ Mesangiocapillary GN

  • Causes
  • Pathology
A
Primary= idiopathic
Secondary causes
- Hep C
- Endocarditis
- Viral infections
- Malaria
- SCD

Pathology
- Deposits in intraglomerular mesangium.

22
Q

Membranoproliferative/ Mesangiocapillary GN

- Presentation

A
  • AKI, CKD

- Nephrotic syndrome

23
Q

Membranoproliferative/ Mesangiocapillary GN

- Treatment

A

Strict BP control

ACE inhibitors for proteinuria >1g/day

Immunosuppression. (similar to crescentic)

  • Steroids
  • CNIs
  • Mycophenolate mofetil
  • Rituximab