Unit 13 Flashcards
Urinary System - Function
Remove waste products-from bloodstream (toxic wastes and unused nutrients)-as urine (e.g.,blood urea nitrogen, creatinine, metabolic end products)Regulate fluid and electrolyte balance-acid/base balance, calcium metabolismRegulate blood pressure-body fluids
Urinary System - Structure
Kidney:-nephrons: site of urine formation-Glomerulus: site of blood filtering-Calyces & pelvis: collect urine from kidneysUreters–tubules between kidney & urinary bladderUrinary bladder-muscular storing urineUrethra-tube between urinary bladder & external opening; longer in males
Normal urine output
1 to 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, +2.5L/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, increase 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
-Congenital Malformation-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
-Congenital Malformation-inherited (genetic)-multiple renal cysts covering both kidneys, filled with clear fluid, few millimeters to few centimeters in diameter-cause massive kidney enlargement (x20), 1lb kidney turns into 20lbs-Adult and Childhood
Adult polycystic disease
caused by autosomal dominant defectcommon in 10% of patients with chronic renal failure; symptomatic after age 30Complications:-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 dieComplications:-often associated with liver cysts & biliary ductal hyperplasia -> cirrhosis like scars-large kidneys prevent expansion of lungs