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

A

VATOR

23
Q

adds cardiac and limb anomalies to the VATER syndrome

A

VAcTERL

24
Q

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

A

ureteropelvic junction obstruction

25
Q

What is the sonographic appearance of the medullary pyramids?

A

hypoechoic and arranged around central sinus

26
Q

The surrounding cortex is quite thin; the echogenicity is ______ or slightly _______ than normal liver parenchyma.

A

similar or slightly greater

27
Q

Renal cortical echogenicity normally decreases less than liver by __ to ___ months of age.

A

4-6

28
Q

The ______ _____ lie at the base of medullary pyramids and appear as intensely echogenic structures.

A

Arcuate arteries

29
Q

Each adrenal gland lies immediately ______ to the upper pole of the kidney

Superior or Inferior?

A

Superior

30
Q

The normal urinary bladder in thin-walled and should measure less than ____ mm

A

3 mm

31
Q

When empty, the wall thickness increases but remains less than ___ mm

A

5 mm

32
Q

If the child is well hydrated then the ____ ____ can be seen

A

distal ureters

33
Q

What are the 3 most common causes of dilation of the collecting system (hydronephrosis)

A

1) Obstruction
2) Reflux
3) Abnormal muscle development

34
Q

What is the most common cause of a bladder outlet obstruction in a male neonate?

A

Posterior Urethral Valves

35
Q

What should we do to determine the severity of the hydronephrosis?

A

1) Determine where it is unilateral/bilateral
2) Determine if the ureters and bladder is dilated
3) Determine status of renal parenchyma

36
Q

What are the sonographic findings of hydronephrosis?

A

Visible renal parenchyma w/ central cystic componenet, small peripheral cysts budding off central cysts and dilated ureter

37
Q

Uteropelvic Junction Obstructions most often result from ??

A

Intrinsic narrowing or extrinsic vascular compression @ level of uteropelvic junction.

38
Q

What are the sonograhpic findings of uteropelvic junction obstruction.

A

Pelvocalyceal dilation w/o ureteral dilation. When the obstruction is pronounced, the dilated renal pelvis extends inferiorly and medially

39
Q

Malignant tumor that arises in sympathetic chain ganglia and adrenal medulla.

A

Neuroblastoma

40
Q

Neuroblastoma occurs between the ages of ___ months to ____ years

A

2 months- 2years

41
Q

What are the sonographic appearance of a neuroblastoma?

A

highly echogenic w/ intrinsic calcifications.

The smaller tumors are homogenous and hypoechoic whereas the larger ones are more complex.

42
Q

What is a good way to differentiate between tumor and adrenal hemorrhage??

A

Put on color Doppler

Neoplastic growths will have increased vascularity.

43
Q

What is the most common malignant renal tumor in young children and what is the typical age range?

A

Wilms’ Tumor

2-5 years of age

44
Q

What is the 2nd most common abdominal tumor

A

Neuroblastoma