Lecture 3: Development of the Digestive Sytem Flashcards

1
Q

The epithelium of the digestive system is made up of what kind of ‘derm; what are the exceptions?

A

Endoderm

*except mouth (1st arch portion) and anal canal = ECTODERM*

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2
Q

The smooth muscle, vasculature, CT, and any cells arising from monocytes are made up of what kind of ‘derm?

A

Mesoderm: splanchnic mesoderm

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3
Q

The autonomic ganglion, post-ganglionic neurons, in the digestive tract arise from which cell type?

A

Neural Crest

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4
Q

What are the boundaries of the foregut, midgut, and hindgut?

A
  • If above the yolk sac, then it’s foregut
  • Same level as yolksac, is migut
  • Below yolksac, is hindgut
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5
Q

What are the derivatives of the Foregut; arterial suppky?

A
  • Pharynx
  • Respiratory system
  • Esophagus
  • Stomach
  • Liver and Pancreas
  • Biliary apparatus
  • Proximal duodenum

*CELIAC TRUNK*

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6
Q

What are the derivatives of the Midgut; arterial supply?

A
  • Small intestine (duodenum)
  • Cecum and veriform appendix
  • Ascending colon
  • Right 1/2 of transverse colon

*SUPERIOR MESENTERIC ARTERY*

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7
Q

What are the derivative of the hindgut; arterial supply?

A
  • Left 1/2 of transverse colon
  • Descending colon
  • Sigmoid colon
  • Rectum
  • Superior anal canal
  • Epithelium of urinary bladder/urethra

*INFERIOR MESENTERIC ARTERY*

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8
Q

What’s a Tracheoesophageal (TE) Fistula; which week does this occur?

A
  • Abnormal migration of the tracheoesophageal folds and formation of the septum = abnormal passage between trachea and esophagus
  • Commonly associated w/ esophageal atresia.
  • Occurs during WEEK 5
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9
Q

What are the presenting signs and symptoms of TE fistula?

A
  • Prenatally: polyhydramnios
  • Birth: coughing, gagging, cyanosis, vomiting, voluminous oral secretions, possible respiratory distress
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10
Q

What is shown in this picture, and what can this tell you?

A
  • This image shows coiling of a NG tube within the esophagus.
  • This indicates an infant has a TE Fistula
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11
Q

What week does the stomach begin to rotate and explain what occurs.

A
  • Week 4
  • At the start the ventral border is to the right and dorsal border is to the left
  • Dorsal wall grows much faster and forms the greater curvature, while the ventral wall forms the lesser curvature
  • Stomach will rotate 90° clockwise about a longitduinal axis, the left side is now ventral, while the right is now dorsal.
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12
Q

What occurs to the left and right vagal nerves during developmental stomach rotation?

A
  • Left vagal nerve becomes anterior
  • Right vagal nerve becomes posterior
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13
Q

When the stomach does 90° of clockwise rotation about the longitudinal axis, what space forms?

A

The lesser sac (omental bursa)

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14
Q

What is Hypertrophic Pyloric Stenosis; common presenting sx?

A
  • Narrowing of pyloric lumen obstructing food passage due tp hypertrophy of the muscularis externa in this region.
  • Immediate post-feeding vomiting that is nonbilous and forceful (projectile vomiting), fewer and smaller stools, failure to gain weight or weight loss
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15
Q

Explain the formation of the liver and biliary system.

A
  • All form from a single diverticulum of gut endoderm
  • Endoderm differentitates into hepatocytes, bile ducts, and hepatic ducts
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16
Q

What happens as the gallbladder begins to elongate; what forms?

A

Forms the cystic duct and where the cystic and hepatic ducts merge forms the common bile duct.

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17
Q

Explain formation of the pancreas

A
  • Develops from 2 distinct buds, dorsal and ventral primordia
  • Dorsal forms the body and tail
  • Ventral forms the head and uncinate process
  • As duodenum rotates to the right, ventral pancreatic bud is carried dorsally
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18
Q

Where do the 2 pancreatic ducts arise from?

A
  • Main pancreatic duct arises from ventral primordia
  • Towards tail pancreatic duct comes from the dorsal primordia
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19
Q

What is Annular pancreas; when would bilious vomit be seen?

A
  • Bifed ventral pancreatic bud will grow out and fuse around the duodenum, causing an obstruction (narrowing).
  • If annulus develops inferior to bile duct, child will have sx’s similar to pyloric stenosis, EXCEPT, the vomit will be bilious

- If obstruction is superior to bile duct, vomit will be non-bilious

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20
Q

Any accessory pancreatic ducts arise from which part?

A

Dorsal pancreatic bud

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21
Q

Explain the rotation of the midgut; how much rotation occurs?

A
  • Due to limited size of the abdomen, lengthening midgut herniates out into umbilicus at 6 weeks, rotating 90°.
  • Comes back in during week 10 and rotates 180°
  • Total of 270° rotation
22
Q

What do the cranial and caudal ends of the gut form at the end of midgut rotation?

A
  • Cranial forms the small intestine
  • Caudal forms the large intestine
23
Q

What is Omphalocele; occurs when?

A
  • Weeks 6-10
  • Herniated bowel does not fully retract back into the abdomen, will be covered w/ an amnion and peritineum membrane
24
Q

What is Gastroschisis; occurs when?

A
  • Week 4
  • Herniation of abdominal contents due to muscular defect in anterior abdominal wall.
25
Q

What is embryologic mechanism of Hirschsprung Disease (aka megacolon)?

A
  • Most common neonatal obstruction
  • Failure of NC to migrate
  • Lack autonomic ganglion cells (from NC) distal to dilated segment: area cannot relax is always constricted
  • Enlarged section is normal
26
Q

What is nonrotation of the midgut?

A
  • Completes first 90° CCW rotation but does not do remaining 180° CCW rotation
  • Ends up with left-sided colon and rightsided small intestines
  • Pt’s may have obstructions
27
Q

What is reversed rotation of the midgut?

A
  • Completes initial 90° CCW but then does a 180° CW rotation

  • Transverse colon ends up posterior to the duodenum, normally the duodenum is posterior to the transverse colon
28
Q

Explain formation of the definitive gut lumen

A
  • Start with hollow gut tube (week 6),
  • Gut tube is then occluded by endodermal proliferation
  • Apoptosis (recanalization) occurs and by week 8 you have now formed the definitive hollow gut.
29
Q

What 2 defects can occur during formation of the definitive gut lumen?

A

1) Duplication - pocket forms in wall of the gut tube
2) Incomplete recanalization = stenosis typically seen in 3rd part of duodenum

30
Q

What is Meckel’s Diverticulum, can lead to?

A
  • Abnormality of the vitelline duct (normally regresses)
  • Projection from the ilium to the abdominal wall
  • Can lead to intestinal obstruction, GI bleeding, bowel sepsis
31
Q

What is the rule of 2’s for Meckel’s Diverticulum?

A
  • 2% of population
  • Found 2 feet from ileocecal junction
  • Usually about 2 inches long
  • 2 types of ectopic tissues: gastric and pancreatic
  • 2:1 ratio of male to female
32
Q

What is a Omphalomesenteric fistula?

A
  • Persistent attachment of vitelline duct to umbilicu, fistula causes poop to leave out of bellybutton
33
Q

What ‘derm layers are the cloacal membrane and urorectal septum composed of?

A

Cloacal membrane = Endoderm and Ectoderm

Urorectal septum = mesoderm

34
Q

What does the urorectal septum do; what happens to the cloacal membrane?

A
  • Migrates down and partitions cloaca into a dorsal anorectal canal and a ventral urogenital sinus.
  • Cloacal membrane ruptures thereby opening both the UG sinus and anal canal to the exterior
35
Q

How do parts of the anal canal differ; what separates the anal canal?

A
  • The anal canal is seprated into 2 distinct parts, one from the hindgut endoderm and the anal pit from ectoderm, separated by the pectineal line
  • Each part has a separate blood and nerve supply
36
Q

What is the neurovasculature of the hindgut endoderm in anal canal?

A
  • Nerves: Autonomic
  • Blood vessels: Inferior mesenteric/superior rectal a.
  • Lymphatics: Inferior mesenteric lymph nodes
37
Q

What is the neurovasculature of the hindgut ectoderm of the anal canal?

A
  • Nerves: Somatic nerve –> Pudendal. Painful hemorrhoids
  • Blood vessels: Iliac –> middle and inferior rectal
  • Lymphatics: Meets at pectineal line. Superior inguinal lymph nodes
38
Q

What is underlying cause of these Anorectal Malformations in figures A and B?

A

A) Proctodeum did not form correctly

B) Proctodeum did not migrate at all

39
Q

What is the underlying cause of the Anorectal Malformations seen in figures D and H?

A

Urorectal septum abnormally divided the tract

40
Q

Differentiate between the pleuropericardial membrane, the pleuroperitoneal membrane and the septum transversum.

A
  • Pleuropericardial folds migrate to midline and are separated from pleural canals by the pleuropericardial folds
  • Septum transversum meets with the pleuroperitoneal membranes and fuses.
  • Tissue from the body wall is then pulled into the diaphragm

*left fuses more slowly*

41
Q

How does the diaphragm form?

A
  • Septum transversum with the central tendon
  • Dorsal mesentary becomes the right and left crus of the diaphragm
  • Peripheral musculature gets pulled off body wall
42
Q

What is shown here and how does this occur, what side does it usually occur on?

A
  • Congenital diaphragmatic hernia
  • Defective formation and/or fusion of the pleuroperitoneal membrane, large opening in posterolateral diaphragm (foramen of Bochdalek)
  • 85-90% occur on the left side
43
Q

What is Mesentery?

A
  • Double layer of serous membrane from splanchinc mesoderm
  • Allow BV’s, nerves, and lymphatics to get to an organ and then back to the body wall.
  • Has a parietal and visceral layer
44
Q

In the Abdominal cavity and liver what does the: dorsal mesogastrium, ventral mesogastrium, and ventral mesentery form?

A

Dorsal mesogastrium - greater omentum (around stomach)

Ventral mesogastrium - lesser omentum (stomach to liver)

Ventral mesentery - falciform ligament (liver to abdominal wall)

45
Q

What are the mesenteries of the mid/hindgut; are they from ventral or dorsal?

A
  • Mesoduodenum - mesentery around duodenum
  • Mesentery proper - containing jejunum and ileum
  • Mesocolon - around transverse colon and sigmoid colon
  • Mesorectum - mesentery around the rectum

*ALL from DORSAL*

46
Q

What is the axis of rotation of the midgut?

A

Superior Mesenteric Artery!!!

47
Q

What are the divisions of the Dorsal mesogastrium?

A
  • Splenorenal (leinorenal) ligament
  • Gastrolienal ligament
  • Greater omentum
48
Q

How is the greater omentum formed?

A
  • As the stomach migrates and rotates, the dorsal mesogastrium is pulled down and rotated
  • You now have fusion of 2 double layers (4 total) of splanchic mesoderm, creating the greater omentum
49
Q

What does fusion of mesenteries with body walls result in?

A

Secondary Retroperitoneal structures

50
Q

Which structures become secondary retropeitoneal?

A
  • Mesogastrium dorsal to spleen (part holding pancreas)
  • Mesoduodeum
  • Ascending mesocolon
  • Descending mesocolon
51
Q

What does it mean for a structure to be intraperitoneal; what are the intraperitoneal structures?

A
  • Anything surrounded by mesentery
  • Stomach
  • Tail of pancrea
  • 1st part of duodenum
  • Jejunum, ileum
  • Transverse Colon
  • Sigmoid Colon
52
Q

We have a mneomic for retroperitoneal structures, using it, indicate which structures are primary and secondarily retroperitoneal?

A

SADPUCKER

S - suprarenal glands (primary)

A - aorta and IVC (primary)

D - duodenum 2nd-4th part (secondary)

P - pancreas, except tail (primary)

U - ureters (primary)

C - colon, ascending/descending (secondary)

K - kidneys (primary)

E - esophagus (primary)

R - rectum (primary)