Chapter 27- Pediatric Adrenal Glands and Kidneys Flashcards

1
Q

occurs when the fetus is stressed during a difficult delivery or a hypoxic insult (lack of oxygen)

A

adrenal hemorrhage

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2
Q

lie at the base of the medullary pyramids and appear as echogenic structures

A

arcuate arteries

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3
Q

congenital polycystic kidney disease that usually presents during middle age; sometimes asymptomatic, the severity of the disease varies widely; presents with hypertension, hematuria, and enlarged kidneys; cysts can also form in the liver, spleen, and pancreas

A

autosomal dominant polycystic kidney disease (ADPKD)

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4
Q

rare, congenital polycystic renal disease also known as infantile polycystic disease; typically presents with diffuse enlargement, sacculations, and cystic diverticula of the medullary portions of the kidneys

A

autosomal recessive polycystic kidney disease (ARPKD)

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5
Q

most common benign renal tumor of the neonate and infant

A

congenital mesoblastic nephroma

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6
Q

the outer rim of the kidney; the cortex is thin in the neonate, with an echogenicity similar or slightly greater than that of the normal liver parenchyma

A

cortex

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7
Q

dilatation of any tubular vessel

A

ectasia

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8
Q

occurs more commonly in females (on left side); ectopic insertion and cystic dilation of distal ureter of a duplicated renal collecting system

A

ectopic ureterocele

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9
Q

dilation of the renal collecting system

A

hydronephrosis

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10
Q

large and hypoechoic in the neonate

A

medullary pyramids

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11
Q

most common cause of renal cystic disease in the neonate; multiple cystic masses within the kidney; may have contralateral ureteral pelvic junction obstruction

A

multicystic dysplastic kidney (MCDK)

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12
Q

abnormal persistence of fetal renal blastema (potential to develop into Wilms’ tumor)

A

nephroblastomatosis

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13
Q

malignant adrenal mass seen in pediatric patients; hemorrhaging tumor principally consisting of cells resembling neuroblasts

A

neuroblastoma

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14
Q

poorly functioning enlarged kidneys

A

polycystic renal disease

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15
Q

the presence of a valve in the posterior urethra; occurs only in male fetuses; most common cause of bladder outlet obstruction in the male neonate

A

posterior urethral valve

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16
Q

classification of cystic renal disease

A

Potter facies

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17
Q

dilation of the fetal abdomen secondary to severe bilateral hydronephrosis and fetal ascites; fetus also has oligohydramnios and pulmonary hypoplasia

A

prune belly syndrome

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18
Q

underdevelopment of the lung tissue that occurs in utero secondary to oligohydramnios

A

pulmonary hypoplasia

19
Q

kidney becomes enlarged and edematous as a result of obstruction of the renal vein

A

renal vein thrombosis

20
Q

most common neonatal obstruction of the urinary tract; results from intrinsic narrowing or extrinsic vascular compression

A

uteropelvic junction obstruction

21
Q

most frequent malignant tumor in the neonate and infant

A

Wilm’s tumor ( nephroblastoma)

22
Q

vertebral, anal, tracheoesophageal fistula, and renal anomalies

23
Q

adds cardiac and limb anomalies to the VATER syndrome

24
Q

What is the most common type of obstruction of upper urinary tract?

A

ureteropelvic junction obstruction

25
What is the sonographic appearance of the medullary pyramids?
hypoechoic and arranged around central sinus
26
The surrounding cortex is quite thin; the echogenicity is ______ or slightly _______ than normal liver parenchyma.
similar or slightly greater
27
Renal cortical echogenicity normally decreases less than liver by __ to ___ months of age.
4-6
28
The ______ _____ lie at the base of medullary pyramids and appear as intensely echogenic structures.
Arcuate arteries
29
Each adrenal gland lies immediately ______ to the upper pole of the kidney Superior or Inferior?
Superior
30
The normal urinary bladder in thin-walled and should measure less than ____ mm
3 mm
31
When empty, the wall thickness increases but remains less than ___ mm
5 mm
32
If the child is well hydrated then the ____ ____ can be seen
distal ureters
33
What are the 3 most common causes of dilation of the collecting system (hydronephrosis)
1) Obstruction 2) Reflux 3) Abnormal muscle development
34
What is the most common cause of a bladder outlet obstruction in a male neonate?
Posterior Urethral Valves
35
What should we do to determine the severity of the hydronephrosis?
1) Determine where it is unilateral/bilateral 2) Determine if the ureters and bladder is dilated 3) Determine status of renal parenchyma
36
What are the sonographic findings of hydronephrosis?
Visible renal parenchyma w/ central cystic componenet, small peripheral cysts budding off central cysts and dilated ureter
37
Uteropelvic Junction Obstructions most often result from ??
Intrinsic narrowing or extrinsic vascular compression @ level of uteropelvic junction.
38
What are the sonograhpic findings of uteropelvic junction obstruction.
Pelvocalyceal dilation w/o ureteral dilation. When the obstruction is pronounced, the dilated renal pelvis extends inferiorly and medially
39
Malignant tumor that arises in sympathetic chain ganglia and adrenal medulla.
Neuroblastoma
40
Neuroblastoma occurs between the ages of ___ months to ____ years
2 months- 2years
41
What are the sonographic appearance of a neuroblastoma?
highly echogenic w/ intrinsic calcifications. The smaller tumors are homogenous and hypoechoic whereas the larger ones are more complex.
42
What is a good way to differentiate between tumor and adrenal hemorrhage??
Put on color Doppler Neoplastic growths will have increased vascularity.
43
What is the most common malignant renal tumor in young children and what is the typical age range?
Wilms' Tumor 2-5 years of age
44
What is the 2nd most common abdominal tumor
Neuroblastoma