KIDNEYS Flashcards
the ______ is the outer renal parenchyma from renal sinus to renal capsule
renal cortex
the ______ is the inner portion of the kidney from the base of pyramids to center of kidney.
renal medulla
the ______ is the inner hyperechoic portion of the kidney which contains fat, calyces, renal pelvis, connective tissue, renal vessels, and lymphatics
renal sinus
the ______ is the anechoic, usually spaced triangles of collecting tubules between cortex and renal sinus. commonly seen in neonatal and pediatric kidneys.
medullary pyramids
the ______ is the funnel-shaped transition from the major calyces to the ureter
renal pelvis
the ______ is the medial opening for entry/exit of artery, vein, and ureter
renal hilum
the ______ is 3 extensions of the renal pelvis
major calyces
the ______ is the extensions of the major calyces that collects urine from the medullary pyramids.
minor calyces
the ______ is the apex of the medullary pyramids.
renal papilla
______ is the fibrous shealth enclosing the kidney and the adrenal glands. this is referred to as the perirenal space.
gerota’s fascia
______ is the functional unit of the kidney consisting of the renal corpuscle, proximal convoluted tubule, descending and ascending limbs of Henle’s loop, distal convoluted tubule, and collecting tubules.
nephron
______ consists of glomerulus and gromerular capsule.
renal corpuscle (malpighian body)
What are the 5 divisions from the main renal artery?
main renal>segmental>interlobar>arcuate>interlobular
the renal variant in which the developing kidneys fuse in the pelvis and one kidney ascends to its normal position, carrying the other one with it across midline.
crossed fused renal ectopia
the renal variant in which the kidneys may fuse to form a round mass in the pelvis.
discoid or pancake kidney
renal variant in which there is cortical thickening on the lateral aspect of the left kidney.
dromedary hump
This defect is also known as fetal lobulation which is partial fusion of the renunculi (embryonic kidney)
junctional parenchymal defect
______ is a renal variant is which the collecting system is duplicated. can be complete (2 ureters) or incomplete (one ureter).
duplex kidney
with complete duplex kidneys, (2 ureters) the upper pole is ureter is inserted ectopically which has a frequent complication of a ______.
ureterocele
a normal variant of prominent renal cortical parenchyma located between two medullary pyramids.
column of bertin (septal cortex)
renal agenesis is associated with ______ and ______.
oligohydramnios
pulmonary hypoplasia
unilateral renal agenesis may be an isolated congenital malformation or may be associated with chromosomal abnormalities. some associations include:
bicornuate or didelphys uteri
seminal vesicle agenesis
congenital cardiac malformations
VACTERL syndrome
VACTERL syndrome
vertebral defects anal atresia cardiovascular anomalies tracheoesophageal fistula renal anomalies limb defects
______ lies outside the renal sinus sonographically appearing as a cystic collection medial to the renal hilum.
extrarenal pelvis
______ is a common cause of urinary obstruction in the male neonatal population.
posterior uretheral valve
______ is an obstruction due to a flap of mucosa that has a slit-like opening in the area of the prostatic urethra.
posterior uretheral valve
posterior uretheral valve sonographic findings include:
large bladder
hydroureter
hydronephrosis
urinoma
most renal cysts are simple cortical cysts that originate from obstructed ______
uniniferous tubules
______ cysts are calyceal diverticula that sonographically appear as simple cysts
pylogenic
______ cysts are cortical cysts that bulge into the central sinus of the kidney
parapelvic
______ cysts are lymphatic in the central sinus.
peripelvic
______ is an inherited renal disease that results in bilateral renal enlargement and microscopic cysts
autosomal recessive polycystic kidney disease (ARPKD)
______ is an inherited disease that results in the development of renal, liver, and pancreatic cysts late in life.
autosomal dominant polycystic kidney disease (ADPKD)
ARPKD may be detected in utero with ______
oligohydramnios
______ refers to the typical physical appearance of a neonate as a direct result of oligohydramnios and compression in utero
potter syndrome
causes of potter syndrome include:
bilat renal agenesis ARPKD ADPKD multicystic renal dysplasia obstructive uropathy (PUV defect) early rupture of membranes
Most common cause of an abdominal mass in newborns is ______
multicystic dysplastic kidney
______ is a form of renal dysplasia resulting in multiple noncommunicating cysts with the absence of renal parenchyma.
MCDK
MCDK is the result of atresia of the ______ during fetal development
ureteropelvic junction
MCDK has been reported in various syndromes such as ______, ______, & ______.
beckwith-wiedemann
trisomy 18
VACTERL
Ureteropelvic junction obstruction is caused by ______, ______, ______
ureteral hypoplasia
high insertion of ureter into renal pelvis
compression by segmental artery
congenital dysplastic cystic dilatation of the medullary pyramids due to tubular ectasia or dysplasia.
medullary sponge kidney
the development of multiple cysts in chronically failed kidneys during long-term hemodialysis
acquired cystic disease
______ presents in the 2nd and 3rd decade of life characterized by retinal and central nervous system hemangioblastomas.
Von Hippel Lindau
______ is a hyperechoic, benign renal tumor, 80% involvement in the rt kidney.
angiomyolipoma
a multi-system genetic disease. classic presentation includes: seizures, mental retardation, and facial angiofibromas
tuberous sclerosis