Fiser Chapter 43 PEDIATRIC SURGERY Flashcards

1
Q

Pulmonary sequestration diagnosis

A

CTA

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2
Q

Pulmonary sequestration most common location

A

Left lower lobe

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3
Q

Drainage system of extralobar versus intralobar pulm sequestration

A

Extralobar systemic

Inralobar pulmonary vein

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4
Q

Congenital lobar emphysema treatment

A

Lobectomy (no chest tube)

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5
Q

Most common lobation of CLE

A

Left upper lobe

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6
Q

Location of bronchogenic cyst

A

Mediastinum (right posterior to carina)

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7
Q

Treatment of bronchogenic cyst

A

Resection of cyst

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8
Q

Mediastinal masses: anterior, middle, posterior

A

Anterior: T-cell lymphoma, teratoma, germ cell tumors, thyroid cancer
Middle: T-cell lymphoma, teratoma, cysts (cardiogenic or bronchogenic)
Posterior: T-cell lymphoma, neuroblastoma, neurogenic tumor

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9
Q

Choledochal cyst types

A

I: Fusiform of entire CBD, tx resection and hepaticoJ

II: True diverticular cyst off CBD, tx resection

III: Distal dilatation involving sphincter or Oddi, tx resection and choledochoJ via duodenotomy

IV: Intra and extra hepatic cysts, tx resection and lobectomy, maybe transplant

V: Intrahepatic (Caroli’s disease), tx lobectomy versus transplant

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10
Q

Neuroblastoma most common location

A

Adrenals, but can occur anywhere along sympathetic chain

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11
Q

Secretory diarrhea, raccoon eyes, hypertension, unsteady gait (opsomyoclonus), increased catecholamines, VMA, HVA, and metanephrines, in child <2 years old

A

Neuroblastoma

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12
Q

Embryological origin of neurblastoma

A

Neural crest cells

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13
Q

Indicators of worse prognosis in neuroblastoma

A

NSE (neuron specific elastase), LDH, HVA, diploid tumors, and N-myc amplification

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14
Q

Most common malignancies in kids

A

Overall: leukemia (ALL)
Solid: CNS tumors
Gen surg: Neuroblastoma if <2 yo; Wilms if >2 yo

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15
Q

Embryology of Meckel’s

A

Persistent vitelline duct (aka omphalomesenteric duct)

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16
Q

Most common cause of painless lower GIB in kids

A

Meckel’s

17
Q

Pyloric stenosis metabolic abnormalities

A

Hypochloremic hypokalemic metabolic alkalosis

Tx: NS boluses until making urine, then switch to D5-NS with 10 mEq of K

18
Q

Age of presentation for intususception

A

3 months to 3 years

19
Q

Etiology of intestinal atresias

A

Intrauterine vascular accidents

20
Q

Most common site of intestinal atresia

21
Q

Associated abnormalities with duodenal atresias

A

Down’s syndrome; cardiac, renal, and other GI abnormalities

22
Q

TEF types

A

A: complete atresia

B: proximal fistula and distal atresia

C: most common, proximal atresia and distal fistula

D: Double fistula

E: H type just fistula

23
Q

VACTERL Syndrome

A
Vertebral
Anorectal (imperforate anus)
Cardiac
TEF
Esophageal
Radius (thumb) or Renal
Limb
24
Q

Approach to TEF repair

A

Right extrapleural thoracotomy

25
Malrotation diagnosis
Upper GI study: duo does not cross midline, duodenojejunal junction displaced to right
26
Treatment of Malro
Ladd procedure: resect ladd's bands, perform counterclockwise rotation (turn back hands of time), place cecum in left lower quadrant, duodenum in RUQ, appendectomy
27
Treatment of meconium ileus
Gastrograffin enema, test for CF
28
Appearance of abdominal x ray of meconium ileus
Dilated loops of small bowel without air fluid levels; ground glass or soap suds appearance
29
Classic presentation of NEC
Bloody stools after first feeding in premature neonates
30
Risk factors for NEC
prematurity hypoxia sepsis
31
Initial tx of NEC
resuscitation, npo, abx, TPN, orogastric tube
32
gastroschisis versus omphalocele
Gastroschisis: to the R of midline, no peritoneal lining Omphalocele: midline with sac; associated congenital anomalies and Cantrell pentalogy (cardiac defects, pericardial defects, sternal cleft or abscess of sternum, diaphragmatic, omphalocele)
33
Hirschsprung's disease diagnosis
Rectal biopsy, absence of ganglion cells in myenteric plexus