Development of GI Flashcards

1
Q

name the yolk sac endoderm derivatives

A
  • epithelial lining and glands
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2
Q

name the splanchnic mesoderm derivatives

A
  • smooth muscle and connective tissue
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3
Q

name the derivatives of the foregut

A
  • pharynx and its derivatives
  • lower respiratory tract
  • esophagus
  • stomach
  • liver
  • billary apparatus
  • pancreas
  • duodenum up to the major duodenal papilla
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4
Q

which artery supplies the foregut structures

A
  • celiac artery
    • also supplies the spleen (not part of foregut dev.)
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5
Q

name the derivatives of the midgut

A
  • duodenum distal to the major duodenal papilla
  • jejunum & ileum
  • cecum and appendix
  • ascending colon
  • right 2/3 of transverse colon
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6
Q

which artery supplies the midgut structures?

A
  • superior mesenteric
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7
Q

name the derivatives of the hindgut

A
  • left 1/3 of transverse colon
  • descending colon
  • sigmoid colon
  • rectum
  • anal canal up to the pectinate line
  • urinary bladder and most of urethra
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8
Q

what artery supplies the hindgut structures

A
  • inferior mesenteric artery
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9
Q

describe congenital hypertrophic pyloric stenosis

A
  • hypertrophy of muscles in the pyloric region -> narrowing (stenosis) of the lumen of pyloric canal
  • stomach becomes distended and its contents are expelled with force aka projective vomiting (no bile though)
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10
Q
A
  1. lesser curvature
  2. greater curvature
  3. region of the pyloric sphincter (pyloric sphincter stenosis seen here)
  4. 1st part of duodenum
  5. 2nd part of duodenum
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11
Q

describe duodenal stenosis vs duodenal atresia

A
  • duodenal stenosis: partial occlusion of lumen due to incomplete recanalization; leads to vomiting which is usually bile stained (if stenosis is distal to bile duct opening)
  • duodenal atresia: complete occlusion of lumen (failure to recanalize), and leads to vomiting immediately after birth
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12
Q
A
  • “double bubble” sign of duodenal atresia
    • 2 bubbles for air in stomach and duodenum
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13
Q

describe the relationship between the duodenum and the pancreas

A
  • the main pancreatic duct traverses the length of the gland to join the common bile duct at the hepatopancreatic ampulla. Together they drain into the duodenum at the major duodenal papilla
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14
Q

describe an annular pancreas

A
  • due to bifid ventral pancreatic bud
    • ring of pancreas encircles the 2nd part of duodenum and causes obstruction
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15
Q

the spleen is derived from ______ between the layers of ______

A

the spleen is derived from mesenchymal cells between the layers of dorsal mesogastrium

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16
Q

contrast nonrotation of the midgut vs reversed rotation

A
  • nonrotation: caudal limb returns first -> small intestine lies to the right; generally asymptomatic
  • reversed rotation: midgut loop rotates clockwise direction. Duodenum lies anterior to the transverse colon & posterior to the superior mesenteric artery
17
Q

describe a subhepatic cecum & appendix

A
  • cecum gets adherent to the liver/doesn’t descend to the iliac fossa
    • may cause difficulty in diagnosis of appendicitis
18
Q

describe mixed rotation and volvulus

A
  • cecum lies inferior the pylorus and is fixed to the posterior abdominal wall by peritoneal bands
    • may cause duodenal obstruction (failure of midgut loop to complete the final 90 degree rotation)
19
Q

describe an omphalocele

A
  • herniation or protrusion of abdominal contents into the base of the umbilical cord
  • embryological defect: persistence of the abdominal herniation
  • in contrast to umbiliac hernia, it is covered by peritoneum
20
Q

describe an umbilical hernia

A
  • embryological defect: incomplete closure of the umbilical ring
  • clinical presentation: soft swelling covered by skin
    • protrudes during crying, coughing and straining and can be easily reduced through the fibrous ring at the umbilicus
    • consists of omentum and small portions of the small intestines
21
Q

describe gastroschisis

A
  • anomaly is due to incomplete closure of lateral folds
  • due to defect near the median plane of the abdominal wall
  • viscera protrudes into the amniotic cavity
22
Q

describe Meckel’s diverticulum

A
  • a fingerlike projection from the ileum, representing retention of the embryonic intestinal stalk
23
Q

describe anal stenosis

A
  • narrowed anal canal
  • the urorecetal septum deviates slightly in a dorsal direction as it grows to fuse with the cloacal membrane, which results in a narrowed anal canal and membrane
24
Q

describe an imperforate anus

A
  • failure of the anal membrane to perforate
25
Q

describe anorectal agenesis

A
  • the most common anorectal anomaly
  • due to incomplete separation of cloaca by urorectal septum
  • there may be a fistula to:
    • the bladder: rectovesical fistula
    • the vagina: rectovaginal fistula
    • the urethra: rectourethral fistula
26
Q

describe rectal atresia

A
  • the anal canal and rectum are present but there is no communication between them
  • may be due to:
    • abnormal recanalization
    • defective blood supply
27
Q

describe Hirschsprung Disease aka congenital megacolon

A
  • absence of autonomic ganglia in the myenteric plexus of the narrowed segment
    • caused by faulty migration of neural crest cells
  • most common cause of neonatal intestinal obstruction
  • aganglionic segment = no peristalsis
28
Q
A

barium swallow; can see dilatation in part of the colon = Hirschsprung disease