Unit 13: Urinary System Flashcards
Function of Urinary System
-Remove waste products
–from bloodstream (toxic wastes & unused nutrients)
–as urine
-Regulate fluid & electrolyte balance
–acid-base balance, calcium metabolism
Regulate blood pressure – body fluids
Structure of Urinary System
- Kidneys
- Urinary Bladder
- Ureter
- Urethra
Nephrons
Site of urine formation
Glomerulus
Site of blood filtering
Calyces & Pelvis
collect urine from kidneys
Ureters
tubules between kidney & urinary bladder
Urinary bladder
muscular organ storing urine
Urethra
tube between urinary bladder & external opening; longer in males
Normal urine output
1-1.5 liters a day
Oliguria
decrease in urine output, same frequency, less than 0.4L/day
due to infections, scar tissue, stones, neoplasms
Anuria
no urine output
due to renal failure, neoplasm, paralysis
Polyuria
increase in urine output, ~2.5 L/day
due to infection, high blood pressure, alcohol, diabetes, hyposecretion of ADH
Hematuria
blood (red blood cells) in urine
due to stones, infection, neoplasms, poisoning
Hemoglobinuria
- hemoglobin in urine,
due to poisons, increased destruction anemia
Glycosuria
sugar in urine, (absent in normal urine)
due to diabetes
Ketonuria
ketones (from burning fat) in urine, (absent in normal urine)
due to diabetes, starvation
Pyuria (pyoturia)
- pus in urine
due to infection, renal stones, polycystic kidney
Uremia
– urine present in blood
renal insufficiency
Horseshoe kidney
fusion of two kidneys at one pole due to abnormal embryogenesis most common anomaly (1 in 500) usually asymptomatic higher risk of kidney disease
Polycystic kidney disease
-inherited (genetic)
multiple renal cysts covering both kidneys
-Cause massive kidney enlargement (x20)
normal kidney 1 lb
Adult polycystic disease
Caused by autosomal dominant defect
Common in 10% of patients with chronic renal failure; symptomatic after age 30
Complications of Adult Polycystic Disease
- chronic inflammation
- fibrosis
- hematuria, chronic UTI, secondary hypertension
- kidney failure
Childhood polycystic disease
Caused by autosomal recessive defect
May appear at birth or after 1 year of age
Develops rapidly
75% of infants die
Complications of Childhood polycystic disease
often associated with liver cysts & biliary ductal hyperplasia
- cirrhosis-like scars
- large kidneys prevent expansion of lungs
Hypoplasia
underdevelopment, small kidney
clinically symptoms start in infancy with polyuria, polydipsia (excessive thirst) & electrolyte disturbances
renal failure ~age of 20
Dysplasia
abnormal development (kidney)
aka. multicystic dysplasia of kidney (MCDK)
–most common cystic malformation of the kidney in infancy
possible causes of congenital dysplasia of kidneys
–genetic factors
–mother’s exposure to certain drugs (drugs to treat seizures or blood pressure); cocaine
Aplasia
complete failure to form an organ (kidney)
Glomerulonephritis
inflammation of glomeruli of cortex
cause of glomerulonerphritis
bacterial (usually strep) or viral infections resulting in formation of antigen-antibody complexes