peds Flashcards

(62 cards)

1
Q

When does pyloric stenosis typically develop?

A

first few weeks of life (2-12 weeks of age)

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2
Q

Gold standard technique to diagnose pyloric stenosis

A

ultrasound

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3
Q

Complications are known to occur to what systems of the body for CDH?

A

GI, pulmonary, neurodevelopmental complications

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4
Q

Most common abnormality associated with gastroschisis

A

intestinal atresia

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5
Q

Findings on ultrasound for pyloric stenosis:

A

pylorus/pyloric channel length usually 16mm or greater

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6
Q

Diagnostic test for Meckel’s diverticulum:

A

99m Tcpertechnetate radioisotope scan

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7
Q

Males with this genetic disorder are known to sometimes have absence of bilateral vas deferens

A

cystic fibrosis

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8
Q

What treatments/interventions are associated with development of necrotizing enterocolitis?

A

antibiotic use and formula feeding

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9
Q

What lateral sacral ratio is considered normal in anorectal malformations that signifies likely fecal continence?

A

sacral ratio >0.7

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10
Q

True or false. Direct hyperbilirubinemia is always found in infants with biliary atresia

A

True

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11
Q

What type of neuroblastoma is associated with subcutaneous metastases and positive bone marrow for small, round blue cells, and massive hepatomegaly from hepatic metastases?

A

4S disease neuroblastoma; usually spontaneously regresses

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12
Q

In esophageal atresia, primary repair can be achieved when the length (gap) is _____

A

2 vertebral bodies or less

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13
Q

procedure used to resect a thyroglossal duct cyst:

A

Sistrunk procedure; involves excising the tract, cyst, and hyoid bone 1 cm to the left and right of midline up to the level of foramen cecum

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14
Q

Which types of neuroblastoma tend to regress over time and do not require operation?

A

infantile cystic and 4S disease neuroblastoma

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15
Q

Which is more common after NEC, small intestinal strictures or large intestinal strictures?

A

large intestinal strictures

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16
Q

True or false. About a quarter of infants with duodenal atresia have congenital heart disease

A

True

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17
Q

Perforation in the intestine in utero resulting in meconium accumulation in the peritoneal cavity:

A

meconium pseudocyst; tx with ex lap and ostomy or peritoneal drains

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18
Q

Appearance of meconium pseudocyst on imaging:

A

calcified walls surrounding meconium (large cyst with air fluid levels and eggshell calcifications)

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19
Q

Study of choice for children suspected of having malrotation or intermittent midgut volvulus

A

upper GI contrast study

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20
Q

Treatment of prepubescent males with undescended testis

A

orchiopexy

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21
Q

Initial cancer risk for undescended testis and long term risk for undescended testis:

A

initial: gonadoblastoma

long term: seminoma

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22
Q

Most common solid organ intraabdominal malignancy in children:

A

neuroblastoma

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23
Q

Histology of neuroblastoma

A

small round blue cells in rosette formations

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24
Q

treatment of duodenal atresia

A

diamond duodenoduodenostomy

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25
treatment of pectus carinatum:
removal of affected costal cartilages and sternal osteostomy with sternal reconstruction (Ravitch procedure)
26
Through what incision are most H type TE fistulas approached?
right neck incision; most are located at the level of the thoracic inlet
27
resuscitation regimen for infants:
5% dextrose in 0.45% saline with 20mEq/L
28
True or false. Gastroschisis defects usually occur to the right of the umbilicus
true
29
True or false. Omphalocele occurs to the right of the umbilicus.
false. occurs through the umbilicus
30
most common incision for repair of CDH
subcostal
31
Management of midgut volvulus is decompression by rotating the bowel ______
counterclockwise
32
Management of violation of duodenal mucosa during pyloromyotomy:
repair mucosal defect and place omental patch; alternatively, close the mucosa and the muscle, rotate pylorus 180 degrees and perform a new pyloromyotomy
33
True or false. R0 resection is not mandatory for neuroblastoma
true
34
Operative principles of Wilm's tumor:
must palpate renal artery for tumor thrombus; tumor rupture should be avoided as it upstages disease and leads to recurrences; requires lymph node staging; acquired von Willebrand disease can lead to intraop bleeding
35
True or false. Recent evidence suggests there is equivalent risk of rebleeding or continued bleeding for either limited segmental resection or simple diverticulectomy in tx of Meckel's diverticulum in children
true
36
True or false. Abnormal intestinal rotation is seen in all patients with gastroschisis or omphalocele
True
37
Electrolyte abnormalities of pyloric stenosis:
hypokalemic, hypochloremic metabolic alkalosis
38
How is the pyloromyotomy made for pyloric stenosis?
longitudinal incision from serosa/extramucosal of pylorus just proximal to the hypertrophied muscle to just proximal to the pyloric vein; extend onto antrum of stomach
39
What abnormality is associated with difficulty in getting ECMO access in CDH patients?
vascular (IJ & carotid) hypoplasia
40
What structure is at risk of injury during high ligation of an inguinal hernia in females?
fallopian tube
41
Primary modality of treatment for 3rd and 4th branchial anomaly fistula that can be visualized
endoscopic cautery or chemical ablation
42
What amplification in neuroblastoma is associated with a good prognosis?
MYCN
43
What amplification in neuroblastoma is associated with a bad prognosis?
TrkA
44
What is secondary to failure of closure of the pleuroperitoneal canal?
congenital diaphragmatic hernia posterolateral - Bochdalek type (most common) anteromedial - Morgagni type; less common
45
Nonfunctional pulmonary tissue fed by an anomalous systemic arterial supply with no connection to the tracheobronchial tree:
bronchopulmonary sequestration
46
Abnormality due to poorly developed alveoli structure resulting in recurrent infections and respiratory compromise:
congenital cystic adenomatoid malformation
47
Failure in development of bronchus cartilage resulting in air trapping with expiration
congenital lobar emphysema
48
True or false. Hirschsprung disease can present in later childhood with chronic constipation after weaning from breastmilk in short segment disease
true
49
treatment of hepatoblastoma:
surgical resection upfront is mainstay followed by chemo; if unresectable/metastatic, give chemo upfront to decrease size
50
Most undescended testes resolve spontaneously in the first ____ of life
6 months
51
where do lymph nodes need to be biopsied for Wilm's tumor:
renal hilum, vena cava, and aorta
52
Drug of choice for PDA
indomethacin
53
Standard operation for biliary atresia:
Roux en Y hepatic portoenterostomy (Kasai procedure)
54
most common location for undescended testes
superficial inguinal ring
55
temporizing measures for infants born with transposition of great vessels:
IV prostaglandin E1 to maintain PDA and then balloon atrial septostomy
56
incomplete recanalization of the duodenum during 8-10 weeks gestation resulting in persistent membranous structure in the lumen of the duodenum that appears like a windsock
duodenal web
57
Diagnosis and tx of duodenal web
UGI with barium; tx with duodenotomy and excision of web
58
complete failure of duodenum to recanalize
duodenal atresia; bilious atresia, double bubble on radiograph
59
True or false. There is no consensus on the indications for lap chole in children with biliary dyskinesia
true
60
True or false. All button battery ingestions should be removed (even gastric)
true
61
True or false. Incidentally discovered malrotation must be surgically managed.
true
62
Steps of Ladd's procedure:
``` untwisting of volvulized bowel release of cecal bands broaden the small bowel mesentery incidental appy place small bowel to right and colon to the left ```