Renal Flashcards
Wilms’ Tumor
most common renal malignancy of young children; proliferation of *metanephric blastema; associated w WT1 mut;
Renal agenesis
Uteric bud fails to develop due to lack of signals to mesenchyme; if unilateral then the remaining kidney compensates (hypertrophy and hyperfiltration), pts are at increased risk for *focal segmental glomerular sclerosis (FSGS)
Multicystic Dysplastic Kidney
abnormal uremic bud-mesenchyme interaction (no interaction = agenesis); this is a form of renal dysplasia where kidney is replaced by cysts; there is no/little functioning renal tissue
Duplex Collecting System
two uteric buds or a bifurcation of a ureteric bud; may lead to poor urine flow, hydronephrosis and UTIs; associated w *vesicoureteral reflux
Vesicoureteral reflux
backward urine flow from bladder to kidneys; leads to recurrent UTIs; primary cause is an abnormal closure of ureterovesical junction (UVJ) and associated w duplex ureters; secondary cause: high bladder pressure - seen in posterior urethral valves
Oligohydramnios
decreased formation in fetal *urine; typically occurs in the 2nd trimester of pregnancy (13-27 weeks)
Posterior urethral valves
only occurs in males; there is tissue (valve) that obstructs the bladder outflow (persistent urogenital membrane); on US you will see dilated bladder and kidneys (both); a cause of Potter syndrome in boys
Horseshoe Kidney
inferior poles fuse; kidneys cannot ascend to pelvis to the retroperotineum; they are trapped by the *IMA; associated w *Turner and Down syndrome
Urachus (allantois)
embryonic structure that connects the dome of the bladder to the umbilicus; should be obliterated at birth to form the *median umbilical ligament; if does not obliterate then can serve as a connection between the bladder and umbilical and can leak urine; can lead to infections and *adenocarcinoma of the dome of the bladder
Special Kidney features
the right kidney is slightly smaller (due to the liver); the left kidney has a longer renal vein and is often taken for transplant
IgA vasculitis
Henoch-Schonlein purpura is a IgA-mediated, leukocytoclastic vasculitis that presents w palpable, arthralgia/arthritis, abdominal pain and/or hematuria; renal involvement is due to mesangial deposition of IgA immune complexes w subsequent mesangial cell proliferation, neutrophilic inflation and glomerular damage
Vitamin D deficiency (rickets)
lack of the vitamin D effect causes hypocalcemia due to inadequate Ca2+ absorption; compensatory rise in PTH leads to increased bone resorption, renal Ca2+ reabsorption and renal phosphorus wasting; PTH also induces 1-alpha-hydroxylase activity leading to elevated 1,25OH
Ototoxicity secondary to loop diuretics
occurs when higher dosages, pre-existing chronic renal disease, rapid IV admin or when used in combination w other ototoxic agents; hearing impairment is usually reversible but may be permanent in some cases
cardiorenal syndrome
decompensated HF involves a vicious cycle of hemodynamic alteration and maladaptive neurohomormal changes resulting from decreased renal perfusion; cardiorenal syndrome is a complication of this cycle, in which back pressure from the failing heart increases renal venous pressure to the point that the glomerular filtration rate drops substantially
primary nocturnal enuresis
bed-wetting at the age >5 w/o prior nighttime urinary continence is caused primarily by a brain maturational delay in the development of bladder control
Carbamazepine induced SIADH
syndrome of inappropriate antidiuretic hormone presents w hypotonic hyponatremia, concentrated urine and envolemia; carbamazepine can cause SIADH by increasing ADH secretion and renal sensitivity to ADH
NSAID-induced acute kidney injury
pts w intravascular volume depletion and CKD depend on renal prostaglandin production to dilate the afferent arteriole and maintain GFR; NSAIDs inhibit PGE synthesis which can cause pre-renal azotemia in at-risk pts
blunt lower abdominal trauma
the dome of the bladder rises into the peritoneal cavity when distended w urine; blunt lower abdominal trauma can abruptly increase intravesical pressure and rupture the bladder dome, spilling urine into the intraperitoneal cavity
Autosomal dominant polycystic kidney disease
AD PKD typically manifests in pts age 40-50 e enlarged kidneys, flank pain and HTN; in newborns the kidneys are normal size and the cysts are too small to be detected; as the cysts enlarge, they compress renal parenchyma and cause symptoms
Minimal change disease (MCD)
MCD is caused by immune dysregulation and overproduction of a glomerular permeability factor, which damages podocytes and decreases the anionic properties of the glomerular basement membrane; resulting in selective loss of albumin in the urine, in contrast to the nonselective proteinuria seen in other forms of nephrotic syndrome
ACEi
ACEi reduce angiotensin II levels and cause efferent arteriole dilation thereby decreasing the GFP and filtration rate; this can precipitate acute renal failure in pts w reduced infrarenal perfusion pressure at baseline (ex: renal artery stenosis, CHF and hypovolemia)
acts on the thick ascending limb of Henle loop
Patiromer MOA
a nonabsorbable cation exchange resin used to tx hyperkalemia; binds colonic K+ in exchange for Ca2+, trapping K+ within the resin where it is then excreted in feces; adverse effects include diarrhea, hypokalemia, hypercalcemia and hypo magnesium
Poststeptococcal glomerulonephritis (PSGN)
presents w edema, HTN and hematuria after a strep infection most children recover completely, but adult pt have a relatively poor prognosis and higher risk for chronic HTN and renal insufficiency
ureter injury
the proximal ureter receives its blood supply from the renal artery whereas the distal ureter is supplied by the superior vesicle artery; circulation to the middle portions of the ureter is variable and anastomotic