Nephrotic syndrome

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Background

  • Clinical syndrome characterized by massive proteinuria, which results in hypoalbuminema, hyperlipidemia, and edema
  • Can be primary (idiopathic) or secondary

Etiologies

Common

Exhaustive

Epidemiology

  • If < 20 years old
    • Minimal change (70%)
    • Membranous (20%)
    • Focal segmental glomerulosclerosis (10%)
  • If > 20 years old
    • Membranous (70%)
    • Minimal change (20%)
    • Focal segmental glomerulosclerosis (10%)

Clinical Manifestations

  • Edema progressing to anasarca
  • Found to have proteinuria, hyperlipidemia, and hypoalbuminemia on investigations

Investigations

  • Urine protein
  • Lipid panel
  • Albumin levels

Diagnosis

  • Significant proteinuria > 3g/day
  • Hyperlipidemia/lipiduria
  • Anasarca
  • Hypoalbuminemia <35g/L

Management

  • If < 20 years old
    • Treat empirically with steroids, as the majority are primary minimal change disease
  • If > 20 years old
    • Needs kidney biopsy to direct treatment