Chapter 16 Flashcards
(41 cards)
kidney functions
- excrete ________ of food metabolism: ____ and other acids are end products of protein metabolism, that only kidneys can excrete
- regulate _____ and _____ balance - by excreting minerals and water that have been ingested in excess of the bodys requirements and conserving them as required
- endocrine function: a hormone called _________ which regulates red blood cell production in bone marrow
waste products urea mineral water eryhropoietin
diagnostic tst for kidney function
1) BUN: ___________
2) _____ levels in blood/urine
3) GFR: __________
blood urea nitrogen
creatinine
glomerular filtration rate
indicates an increased amount of urine
polyuria
a decreased daily output of urine
oliguria
a state in which no urine is produced
anura
presence of increased protein in the urine
proteinuria
presence of increased glucose in urine
glucosuria
presence of blood in uria
hematuria
presence of pus in urine
pyuria
painful and burning urination
dysuria
developmental disorders
________ (not formed)- bilateral (________: deadly) or unilateral which leads to ______ of existing kidney and _______ increases risk of renal failure later in life
renal agenesis
potter syndrome
hypertrophy
hyperfiltration
fusion of kidneys at the lower pole
horseshoe kidney
unilateral: cysts are embedded in connective tissue. the disorder usually occurs in one kidney
multi cystic renal dysplasia
caused by presence of two abnormal genes. lot of cysts (___ filled) , wieght of kidney close __ kg
- autosomal _____ form presents in young adults as hypertension (due to increased ____), ____ and worsening renal failure
- due to mutation in the ____ or ____ gene; cysts develop over time
- _______, _______ cysts, and ______ prolapse
ADPKD (Autosomal Dominant polycystic kidney disease) water 1 dominant renin hematuria APKD1, APKD2 berry aneurysm, hepatic mitral valve
very rare, slightly enlarged kidney and renal failure in ______
ARPKD (autosomal recessive polycystic disease)
infancy
massive proteinuria is generally characterized by excretion of more than ___ grams of protein per day. unlike disorders with greater distruption of glomerular structure, proteinuria in this syndrome is __________ by increased urinary ___ or ___ cells
- _________ (low alubumin) results from proteinuria and is often marked by a serum concentration of less than __ g/100 mL
- edema results from decreased ___________ pressure
nephrotic syndrome 4 unaccompanied red white hypoalbuminemia 3 plasma colloid oncotic
Caused by deposit of ___ deposition in mesangium
of glomeruli & most common nephropathy
worldwide
• May occur due to severe bacterial or viral infection
pathogenesis- not well known
• Microscopic findings show IgA deposits over the
____ area.
• Symptoms- ____ and _____ in urine.
• Treatment: ___ inhibitors and _____
Berger's disease IgA cortex blood, protein ACE, steroids
Autoimmune disease. Is caused by an antiglomerular
basement membrane (anti-GBN). This
reacts with _____ and GBN leading to ______
hemorrhage and ________ This antibody
is ____
Goodpasture syndrome alveolar pulmonary glomerulonephritis IgG
it is the prototype of nephritic syndrome. it is an immune complex disease with the antigen of streptococcal origin
This disorder most often follows or accompanies
infection with nephritogenic strains of group _____________Unlike rheumatic fever, which
chiefly follows streptococcal tonsillitis, it can also
occur after ____ infections.
• Presents 2-3 weeks after infection as ______
(cola-colored urine), oliguria, hypertension, and
______ edema
• ______ recovery in almost all children and many
adults follows. A very small minority develops rapidly
progressive glomerulonephritis
poststreoptococcal glomerulonephritis AB hemolytic streptococci hematuria perioribital complete
This disease is hereditary nephritis associated
with nerve deafness and ocular disorders, such
as lens _______ and _______.
• Clinical characteristics include the _______
syndrome, often progressing to end-stage renal
disease by ___ years of age.
• The cause is a mutation in the gene for the ___
chain of type __ collagen.
• Results in ____ and _____ of the glomerular
basement membrane
alport syndrome dislocation cataracts nephritic 30 a5 IV thinning splitting
Clinical characteristics include slow progression to
chronic renal disease.
• Histologic characteristics include both basement
membrane ________ and cellular proliferation with a
characteristic ______ appearance best seen with
_____ stains.
• Divided into two types based on location of deposits
• Type I (________deposits): associated with
____ and _____
• Type II (________ disease):associated with
overactivation of _______ system.
• Poor response to ______s; progresses to chronic
renal failure
membrano-proliferative glomerulonephritis thickening tram-track silver subendothelial HBV, HCV dense deposit complement steroids
It is a major cause of nephrotic syndrome and is
clinically similar to minimal change disease,
although it occurs in both _____ and older
_______
• It should be suspected in cases of presumed
minimal change disease which do not respond to
_____
• It is more common in ______ and is
associated with ____
• Poor prognosis to _____ and resulting in chronic
renal failure.
focal segmental glomerulosclerosis children parents steroids African Americans HIV steroids
Nodular and diffuse thickening of glomerular
basement membranes
• Electron microscopy demonstrates a striking increase
in thickness of the ______ basement membrane.
Thickening of ______ basement membranes
observable by electron microscopy is one of the
earliest morphologic changes in _______
• An increase in _____ matrix results in two
characteristic morphologic patterns: a) ______
glomerulosclerosis is marked by a diffusely
distributed increase in mesangial matrix,
b) _________
glomerulosclerosis is marked by nodular
accumulations of mesangial matrix material
_________ nodules).
diabetic nephropathy glomerular vascular diabetes mellitus mesangial diffuse nodular Kimmelstiel-Wilson nodules
calcium phosphate or calcium oxalate stones (75%)-Increase of Ca concentration.
calcium stones