renal pathology 1 Flashcards
mesangial cells
- structural support
- phagocytic activity
- secrete bioactive molecules
macula densa
in distal convuluted tubule
sensory cells responsible for detecting sodium concetration
azotemia
elevated BUN and creatinine ( cr more sensitive to kidney dz)
nitrogen
nephritic syndrom
visible blood in the urine
nephrotic syndrome
protein urea > 3.5 g/day
acute renal failure
oliguria/anuria + azotemia
chronic renal failure + stages
prolonged symptoms of uremia
- diminished renal reserve= 50% GFR
- renal insufficincy= GFR 20-50%. hypertnesion
- GFR 20-25% edema, neuro and cardio problems
- end stage- GFR <5%. temrinal uremia
unilateral agenesis of kidney
beingn. remaining kidney enlarged. may get glomerular sclerosis
kidney hypoplasia
do not develop to normal size
reduced # of lobes and pyramids
cystic renal dysplasia
immature collecting ducts
cysts lined with flattened epithelium
normal and abnormal nephrons
adult onset polycystic kidneys
autosomal dominant large and multicystic liver cysts high rate of proliferation and apoptosis cysts press on glomeruli and arteries= suffocation berry aneurysms chronic renal failure age 40-60 hematuria, flank pain, UTI, htn, renal stones
childhood onset polycystic kidney
recessive.
cysts at right angles to cortical surface
enlarged cystic kidneys at birth
will have kidney liver and pancreas issues (hepatic fibrosis)
will not survive.
kidneys large with smooth surface
cysts of cortex and medulla
medullary sponge kidney
asymptomatic until calcifies Ca salt precipitates due to low pH cysts lined with cuboidal/ transitional epithelium hematuria, UTI, renal stones benign
adult onset medullary cystic disease complx
small kidney with contracted granular surface
cysts in medulla and corticomedullary junction
ocular lesions
salt wasting, polyuria
benign
familial juvenile nephronophthisis
recessive
corticomedullary cysts and shrunken kidney
salt wasting, polyuria, growth retardation, anemia
progressive renal failure from childhood