renal path Flashcards
elevation of the blood urea nitrogen (BUN) and creatinine levels, due to decreased filtration of blood through the glomeruli (decreased glomerular filtration rate)
azotemia
association of azotemia with clinical signs and symptoms, including gastroenteritis, peripheral neuropathy, pericarditis, dermatitis, hyperkalemia, and metabolic acidosis
uremia
most common feature of acute nephritic syndrome
acute onset of hematuria
most common feature of nephrotic syndrome
heavy proteinuria (> 3.5 g per day)
most common feature of acute renal failure
oliguria (or anuria)
AD (adult) polycystic kidney disease is characterized by _____ in both kidneys
multiple expanding cysts
defective gene for adult polycystic kidney disease is _____ located on chromosome 16; the gene encodes for _____
PKD1; polycystin-1
AR (childhood) polycystic kidney disease is due to mutations in the _____; defective protein is _____
PKHD1; fibrocystin
nephrotic syndrome is caused by increased _____ to plasma proteins
glomerular capillary permeability
4 major causes of nephrotic syndrome
- minimal change disease
- focal and segmental glomerulosclerosis
- membranous nephropathy (glomerulonephritis)
- glomerular disease in diabetes mellitus
nephritic syndrome characterized by acute onset of:
- hematuria
- oliguria and azotemia
- hypertension
causes of nephritic syndrome
- acute postinfectious (poststreptococcal) glomerulonephritis
- IgA nephropathy
renal disease affecting tubules, interstitium, and pelvis and is most often secondary to bacterial infection; includes suppurative inflammation of the kidney and renal pelvis
acute pyelonephritis or tubulointerstitial nephritis
acute pyelonephritis is characterized by sudden onset with pain at ______ and systemic evidence of infection; often there is accompanying ______
costovertebral angle; dysuria, frequency, and urgency
clinical and pathologic condition where renal function declines rapidly with evidence of tubular epithelial damage/necrosis
acute tubular necrosis
acute tubular necrosis causes acute kidney injury that leads to ______
decreased GFR, oliguria (low urine output), and electrolyte abnormalities
causes of acute tubular necrosis
severe trauma, ischemia (shock)/DIC , septicemia, and toxins
kidneys are symmetrically atrophic, with moderate reduction in size; kidney surface has an even fine granularity and the cortex is thin
arterionephrosclerosis
_____ and _____ are contributing factors to arterionephroscerosis
hypertension; diabetes
in arterionephrosclerosis, there is narrowing of the lumens or arterioles and arteries caused by _____ and ______
hyaline type of arteriolosclerosis; fibroelastic hyperplasia of muscular arteries
relatively rapid onset of renal failure with increased intracranial pressure leading to headache, nausea, vomiting, and visual impairment
arterionephrosclerosis assoc with malignant hypertension
in arterionephrosclerosis assoc with malignant hypertension, arterioles show ______, reducing blood flow and causing necrosis of glomeruli
hyperplastic arteriolosclerosis
acquired defect in ADAMTS 13, a plasma protease that degrades vWF multimers
thrombotic thrombocytopenia purpura (TTP)
endothelial cell injury which, in most cases, is due to a Shiga-toxin from E.coli; injury leads to platelet activation
hemolytic-uremic syndrome (HUS)
TTP and HUS are both types of _____
thrombotic microangiopathies
one of the more common cancers in children ages 2-5; characterized by abdominal mass; risk is greatly increased in some inherited syndromes
Wilm’s tumor
major clinical renal syndromes
acute nephritic syndrome, nephrotic syndrome, acute renal failure
acute nephritic syndrome characterized by:
proteinuria (mild/moderate), HEMATURIA, and hypertension
nephrotic syndrome characterized by:
SEVERE PROTEINURIA (> 3.5 g/day), low serum albumin, anasarca, high serum lipid, lipiduria
acute renal failure characterized by:
sudden onset of azotemia with OLIGURIA/ANURIA
congenital cystic renal diseases
autosomal dominant (adult) polycystic kidney disease autosomal recessive (childhood) polycystic kidney disease
most obvious clinical sign of nephrotic syndrome
severe edema
most common cause of nephrotic syndrome in children (2/3 of all cases)
minimal change disease
_____ can be seen in EM with minimal change disease
effacement of epithelial cell foot processes
usually occurs in children and young adults; hematuria is noted 1-2 days after non-specific upper respiratory tract viral infection
IgA nephropathy (cause of nephritic syndrome)
acute clinical syndrome; progressive loss of renal function; lab finding consistent with nephritic syndrome; severe oliguria
crescentic or rapidly progressive glomerulonephritis
interstitial infiltration of mononuclear inflammatory cells, often with neutrophils and many eosinophils
drug-induced interstitial nephritis