Embryology Flashcards

1
Q

What develops from the foregut?

A

esophagus, stomach, ⅓ of duodenum, liver, gallbladder, biliary ducts, pancreas

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2
Q

What develops from the midgut?

A

⅔ of duodenum, jejunum, ileum, cecum, appendix, ascending colon, ⅔ trans colon

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3
Q

What develops from the hindgut?

A

⅓ trans colon, descending colon, sigmoid colon, rectum, proximal anal canal

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4
Q

What develops from the dorsal mesentery?

A

greater omentum, gastrospenic lig, gastrocolic lig, gastrophrenic lig, splenorenal lig, mesocolon, “the mesentery”

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5
Q

What develops from the ventral mesentery?

A

hepatogastric lig, hepatoduodenal lig, falciform lig, coronary lig

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6
Q

What is different between where the dorsal and ventral mesenteries are found?

A

ventral mesentery only in abdominal foregut

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7
Q

Where is the hepatic diverticulum?

A

ventral mesentery

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8
Q

What does the hepatic diverticulum form?

A

liver, gallbladder, dorsal pancreatic bud

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9
Q

What is an annular pancreas?

A

ventral pancreas is around duodenum; bad only when inflamed

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10
Q

How does the spleen form?

A

spleen forms by aggregation of epithelial and hematopoietic cells within dorsal mesentery

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11
Q

What causes duodenal stenosis? pyloric stenosis?

A
  • duodenal stenosis: failure to recanalize duodenum → bilious vomit
  • pyloric stenosis: hypertrophy of pyloric muscle
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12
Q

What is Meckel’s Diverticulum?

A

partial persistence of the omphalomesenteric duct with proximal patency
common: 2-3% of pop
most commonly 2 ft from ileocecal valve on anti-mesenteric border
30-50% contain gastric mucosa capable of making acid and gastric enzymes
clinical:
rectal bleeding,
vomiting-bowl obstruction,, acute abdominal pain

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13
Q

What is “pyloric stenosis”? What will you see?

A
post-natal “developmental defect” w/ hypertrophy and hyperplasia of muscle layers
clinical:
3-12 wk onset
non-bilious, projectile emesis
weight loss
hyperperistaltic waves
palpable “pyloric olive”
hypoCl-, K-
metabolic alkalosis
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14
Q

What is duodenal atresia/stenosis and what do you see?

A

early embryologic defects so see other anomalies: 30% Down Syndrome
complete (atresia) or incomplete (stenosis, web, diaphragm) obstruction
80% distal to ampulla of vatar → bilious vomiting
AXR: “double bubble sign” - gastric and duodenal w/ absent distal gas

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15
Q

What is Malrotation and Midgut Volvulus - and what do you see/do?

A

failure of normal rotation of intestine → arrest of cecum in abnormal site with formation of adhesions Ladd’s Bands to posterior peritoneal wall → obstruction
symps: bilious emesis, rectal bleeding
if small bowel occlude SMA → EMERGENCY ischemic necrosis
major cause of short bowel

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16
Q

What do you seen in intestinal obstruction in newborn ? Upper vs lower?

A

inc intraluminal P → decreased venous and arterial blood flow
if untreated can lead to necrosis, perforation, peritonitis
complete: early symps (24-48 hrs)
incomplete: variable
history: polyhydramnios, toxemia, bleeding, viral infection diabetes, CF
symps: bilious vomit, distension, delayed/absent meconium passage, increased gastric aspirate (>15 ml)
upper part: early onset, decreased distal
lower: after 24 hrs age, multiple air-filled loops of bowel; “micro colon” on barium enema