Nephrotic syndrome
Description
Kidney disorder characterized by marked proteinuria, hypoalbuminemia, hyperlipidemia, increased coagulation, and edema
Results from a glomerular defect that affects permeability, indicating renal damage
Prognosis highly variable, depending on underlying cause
Some forms possibly progressing to end-stage renal failure
In children, 1 in 50,000 new cases per year
In children, peak incidence between ages 2 and 3
Slightly more common in males than in females
Pathophysiology
Glomerular protein permeability increases.
Urinary excretion of protein, especially albumin, increases.
Hypoalbuminemia develops and causes decreased colloidal oncotic pressure.
Leakage of fluid into interstitial spaces leads to acute, generalized edema.
Vascular volume loss leads to increased blood viscosity and coagulation disorders.
Renin-angiotensin system is triggered, causing tubular reabsorption of sodium and water and contributing to edema.
Causes
Certain neoplastic diseases such as multiple myeloma
Circulatory diseases
Collagen-vascular disorders
Focal glomerulosclerosis (developing spontaneously at any age, occurring after kidney transplantation, or resulting from heroin injection; developing in about 10% of childhood cases and up to 20% of adult cases)Stay updated, free articles. Join our Telegram channel
Full access? Get Clinical Tree