Generalised swelling Flashcards

1
Q

List the complications of nephrotic and nephritic syndrome.

A

NEPHROTIC

  • Hypovolaemia
  • Ascites
  • Pleural effusions
  • Peritonitis

NEPHRITIC

  • Acute renal failure
  • Pulmonary oedema due to heart failure
  • Hypertensive encephalopathy
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2
Q

What are the 5 main causes of generalised swelling?

A
  1. Nephritis
  2. Nephrosis
  3. Allergic reactionsincluding urticara, angioedema etc
  4. Cardiac failure
  5. Malnutrition
  6. Other causes of hypoalbuminaemia
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3
Q

Causes of haematuria in children?

A
  • Post strep GN
  • Polycystic kidneys
  • Renal stone
  • Renal tumour
  • Sickle cell disease
  • Renal trauma
  • UTI
  • Orthostatic proteinuria - after exercising/standing
  • Acute renal failure
  • Nephrotic syndrome
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4
Q

Signs of nephrotic vs nephritic syndrome?

A

NEPHROTIC

  • Proteinuria
  • Oedema
  • Hypoalbuminaemia
  • Hyperlipidaemia

NEPHRITIC

  • Haematuria
  • Oedema
  • Hypertension
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5
Q

What is IgA nephropathy?

A
  • Berger’s disease
  • most common form of nephropathy worldwide
    • abnormal IgA forms
    • IgG targets IgA, creating immune complexes
    • immune complexes travel through the blood
    • IgA-IgG immune complexes deposit in the mesangium = activation of the alternate complement pathway = release of proinflammatory cytokines + macrophages into the kidney
    • = glomerular injury = haematuria
  • typically seen in childhood - microscopic or gross haematuria
  • develops during infection of mucosal lining eg. GIT or resp infections
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6
Q

What is PSGN?

A

Post strep glomerulonephritis

  • IgG/IgM antibodies attack group A beta-haemolytic strep = immune complexes form
  • deposits end up in the glomerular basement membrane (GBM)
  • inflammatory reaction in the glomerulus
    • C3 complement
    • cytokines
    • oxidants
    • proteases
    • = damage to the podocytes
    • = RBCs + proteins are able to filter through
  • cola urine, oliguria, proteinuria, peripheral + periorbital oedema
  • typically affects children
    • 6 weeks after skin infection (impetigo)
    • 1-2 weeks after throat infection (pharyngitis)
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7
Q

What is rapidly progressive glomerulonephritis?

A

crescentic glomerulonephritis

  • not a seperate disease - any GN may result in RPGN
  • leads to renal failure within weeks-months
  • some cases are idiopathic
  • type 1 - antiglomerular membrane antibodies (anti-GBM), Goodpasture syndrome
  • type 2 - caused by immune complex, eg. PSGN, SLE, IgA nephropathy, henoch-scholein purpura
  • type 3 - pauli-immune; no anti-GBM or immune complexes
  • proliferation of epithelial cells into a thick crescent moon shape, can undergo sclerosis/scarring
  • low GFR, can quickly lead to acute renal failure
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8
Q

What is MPGN?

A

Membranoproliferative glomerulonephritis

  • presents as nephrotic syndrome, occasionally nephritic
  • type 1 - most common
    • 1) circulating immune complexes - due to chronic infection (eg. Hep B)
    • immune complexes travel to glomerulus
    • activation of complement pathway
    • 2) inappropriate activation of the complement pathway = no immune complexes
  • thickening of basement membrane, proliferation of mesangial cells
    • type 2 - only involves complement deposit
    • IgG auto-antibody - nephritic factor
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9
Q

What is membranous glomerulonephropathy?

A

aka. wire loop nephropathy
* nephrotic syndrome

PRIMARY
Auto-Ab to podocyte Ag (Phospholipase A2)
SECONDARY (more common)
▪ Infections = HBV, Malaria
▪ Autoimmune = SLE
▪ Drugs = NSAIDs, captopril
▪ Inorganic Salts = Gold, Mercury,

Pathogenesis:
→ Ab against podocyte Ag (or planted Ag)
→ Subepithelial Ig deposits
→ Directly activates Complement (C5b-C9 + MAC).
→ Only proteinuria, no inflammation

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