ped git surgery 2 Flashcards

(52 cards)

1
Q
A
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2
Q

What is an omphalocele?

A

A congenital defect of the abdominal wall at the umbilicus, where abdominal contents herniate into a sac covered by peritoneum and amnion.

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3
Q

What are the contents of an omphalocele sac?

A

Usually liver, stomach, intestines, and sometimes other organs.

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4
Q

What is gastroschisis?

A

A congenital full-thickness abdominal wall defect, typically to the right of the umbilicus, through which intestines freely protrude without a covering sac.

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5
Q

What covers the herniated bowel in gastroschisis?

A

Nothing — the bowel is exposed directly to amniotic fluid.

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6
Q

What is the incidence of omphalocele?

A

Approximately 1 in 4000–6000 live births.

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7
Q

What is the incidence of gastroschisis?

A

Approximately 1 in 2000–3000 live births.

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8
Q

Which is more commonly associated with other anomalies: omphalocele or gastroschisis?

A

Omphalocele.

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9
Q

Which abdominal wall defect is more associated with chromosomal anomalies?

A

Omphalocele.

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10
Q

Which abdominal wall defect is more often isolated?

A

Gastroschisis.

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11
Q

What chromosomal anomalies are commonly associated with omphalocele?

A

Trisomy 13, 18, and 21.

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12
Q

What syndromes are associated with omphalocele?

A

Beckwith-Wiedemann syndrome, pentalogy of Cantrell.

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13
Q

What is the embryological basis of omphalocele?

A

Failure of the midgut to return to the abdominal cavity during week 10 of gestation.

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14
Q

What is the embryological cause of gastroschisis?

A

Vascular disruption of the right omphalomesenteric artery leading to abdominal wall disruption.

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15
Q

What maternal serum marker is elevated in both omphalocele and gastroschisis?

A

Alpha-fetoprotein (AFP).

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16
Q

Which defect is more associated with low birth weight and prematurity?

A

Gastroschisis.

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17
Q

How are omphalocele and gastroschisis diagnosed prenatally?

A

Ultrasound.

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18
Q

What does prenatal US show in omphalocele?

A

Midline abdominal wall defect with a membrane-covered sac containing abdominal contents.

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19
Q

What does prenatal US show in gastroschisis?

A

Free-floating loops of bowel outside the abdomen, usually to the right of the umbilicus.

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20
Q

How should an omphalocele be managed at birth?

A

Cover sac with sterile, non-adherent dressing

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21
Q

How should gastroschisis be managed at birth?

A

Cover exposed bowel with warm saline-soaked gauze and plastic wrap

22
Q

What initial investigations are needed in omphalocele?

A

Echocardiography, renal US, karyotyping, assessment for associated anomalies.

23
Q

What anomalies must be excluded in omphalocele?

A

Cardiac, renal, neural tube defects, and chromosomal anomalies.

24
Q

What is the treatment for small omphalocele?

A

Primary closure.

25
How is a giant omphalocele managed?
Staged silo reduction followed by delayed closure or epithelialization with topical therapy.
26
How is gastroschisis typically repaired?
Primary closure if possible
27
Why is staged repair sometimes needed in gastroschisis?
Because the abdominal cavity is small and bowel is often edematous.
28
What complication is common in gastroschisis?
Prolonged ileus, malabsorption, and necrotizing enterocolitis.
29
Why is TPN often required postoperatively in gastroschisis?
Due to bowel dysmotility and feeding intolerance.
30
What is umbilical hernia?
A midline defect at the umbilical ring allowing protrusion of abdominal contents, covered by skin.
31
What is the incidence of umbilical hernia?
Common — occurs in ~10% of infants.
32
What is the usual management of umbilical hernia?
Observation — most close spontaneously by age 2–3 years.
33
When is surgery indicated for umbilical hernia?
If persists beyond 4–5 years or is symptomatic/incarcerated.
34
What is prune belly syndrome?
A syndrome with deficiency of abdominal wall musculature, urinary tract anomalies, and bilateral cryptorchidism.
35
What is the urachus?
A remnant of the allantois that connects the fetal bladder to the umbilicus.
36
What is a patent urachus?
Persistence of the urachal lumen, forming a direct connection between bladder and umbilicus.
37
What is the presentation of a patent urachus?
Urine drainage from the umbilicus.
38
What is an urachal sinus?
Blind-ending tract from the umbilicus — no communication with the bladder.
39
What is the treatment for urachal anomalies?
Surgical excision of the urachal remnant.
40
What is the omphalomesenteric duct?
Embryologic connection between yolk sac and midgut.
41
What is Meckel’s diverticulum?
Remnant of the omphalomesenteric duct on the ileum — may cause bleeding or obstruction.
42
What is an omphalomesenteric fistula?
Complete patency of the duct — fecal drainage from umbilicus.
43
How are omphalomesenteric duct anomalies treated?
Surgical resection.
44
What is bladder exstrophy?
A defect in the lower abdominal wall and bladder resulting in exposed bladder mucosa through the abdominal wall.
45
What is cloacal exstrophy?
Severe defect where bladder, intestines, and genital structures are exposed on the abdominal surface.
46
What anomalies are associated with cloacal exstrophy?
Imperforate anus, spinal defects, ambiguous genitalia.
47
How is bladder exstrophy managed?
Staged surgical reconstruction.
48
What prenatal sign suggests exstrophy?
Non-visualized bladder on ultrasound.
49
What’s the key difference between gastroschisis and omphalocele in terms of sac?
Omphalocele has a sac, gastroschisis does not.
50
What’s the key difference between gastroschisis and omphalocele in location?
Gastroschisis is right of umbilicus
51
Which has higher risk of chromosomal anomalies: omphalocele or gastroschisis?
Omphalocele.
52
Which has a better prognosis: omphalocele or gastroschisis?
Gastroschisis if isolated and repaired successfully.