Generalised swelling Flashcards
List the complications of nephrotic and nephritic syndrome.
NEPHROTIC
- Hypovolaemia
- Ascites
- Pleural effusions
- Peritonitis
NEPHRITIC
- Acute renal failure
- Pulmonary oedema due to heart failure
- Hypertensive encephalopathy
What are the 5 main causes of generalised swelling?
- Nephritis
- Nephrosis
- Allergic reactionsincluding urticara, angioedema etc
- Cardiac failure
- Malnutrition
- Other causes of hypoalbuminaemia
Causes of haematuria in children?
- 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
Signs of nephrotic vs nephritic syndrome?
NEPHROTIC
- Proteinuria
- Oedema
- Hypoalbuminaemia
- Hyperlipidaemia
NEPHRITIC
- Haematuria
- Oedema
- Hypertension
What is IgA nephropathy?
- 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
What is PSGN?
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)
What is rapidly progressive glomerulonephritis?
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
What is MPGN?
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
What is membranous glomerulonephropathy?
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