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