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Embryological Anatomy of the Embryological Anatomy of the Gastrointestinal Tract Gastrointestinal Tract Lawrence M. Witmer, PhD Lawrence M. Witmer, PhD Department of Biomedical Sciences College of Osteopathic Medicine Ohio University  Athens, Ohio 45701 [email protected] Handout download: http://www.oucom.ohiou.edu/dbms-witmer/gs-rpac.htm 22 January 2002 Arpon Files 2013

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Embryological Anatomy of theEmbryological Anatomy of theGastrointestinal Tract Gastrointestinal Tract 

Lawrence M. Witmer, PhDLawrence M. Witmer, PhD

Department of Biomedical Sciences

College of Osteopathic MedicineOhio University

 Athens, Ohio 45701

[email protected]

Handout download:

http://www.oucom.ohiou.edu/dbms-witmer/gs-rpac.htm

22 January 2002

Arpon Files 2013

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Overview• Digestive tract divided into segments based on vascular supply

• Foregut (esophagus, stomach, part of duodenum, biliary apparatus): celiac artery

• Midgut (rest of small & large bowel up almost to splenic flexure): superior mesenteric artery

• Hindgut (rest of large bowel to superior part of anal canal): inferior mesenteric artery

• Dorsal and ventral mesenteries and their fates• Ventral mesentery: mostly breaks down, except lesser omentum & falciform ligament

• Dorsal mesentery: mostly retained, forming greater omentum & other named mesenteries

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Case Presentation

Choking and continuous coughing were observed in

a newborn infant. There was an excessive amountof mucous secretion and saliva in the infant’s

mouth, who experienced considerable difficulty in

breathing. The pediatrician was unable to pass acatheter through the esophagus into the stomach.

Radiography demonstrated air in the infant’s

stomach.

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Case Presentation

Choking and continuous coughing were observed in

a newborn infant. There was an excessive amountof mucous secretion and saliva in the infant’s

mouth, who experienced considerable difficulty in

breathing. The pediatrician was unable to pass acatheter through the esophagus into the stomach.

Radiography demonstrated air in the infant’s

stomach.

Esophageal atresia with tracheoesophageal fistula

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Development of Esophagus

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Esophageal Atresiawith Tracheoesophageal (TE) Fistula

most common TE fistula

other varieties of TE fistulae

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Case Presentation

 A female infant was born prematurely at 32

weeks’ gestation to a 39-year-old woman whose

pregnancy was complicated by polyhydramnios.

 Amniocentesis at 16 weeks showed that the

infant had trisomy 21. The baby began to vomit

within a few hours after birth; the vomitus

contained bile. Marked dilation of theepigastrium also was noted. Radiographs of the

stomach showed gas in the stomach and the

superior part of the duodenum, but no other intestinal gas was observed.

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Duodenal atresia

Case Presentation

 A female infant was born prematurely at 32

weeks’ gestation to a 39-year-old woman whose

pregnancy was complicated by polyhydramnios.

 Amniocentesis at 16 weeks showed that the

infant had trisomy 21. The baby began to vomit

within a few hours after birth; the vomitus

contained bile. Marked dilation of theepigastrium also was noted. Radiographs of the

stomach showed gas in the stomach and the

superior part of the duodenum, but no other intestinal gas was observed.

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Development of the Duodenum I

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Development of the Duodenum II: Stenosis & Atresia

• Proliferation of epithelium

• Recanalization of lumen• Defective vacuolization

• Duodenal stenosis

• small lumen

• usually 3rd or 4th part

• Duodenal atresia• occluded lumen

• usually 2nd or 3rd part

• 1/4 also have Down’s

• Familial Duodenal Atresia:

autosomal recessive

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Development of the Pancreas

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Development of the Pancreas: Anular Pancreas• Bifid ventral pancreatic bud

• One part rotates normally with bile duct, the other part remains ventral

• Dorsal and ventral parts fuse, forming a ring around descending (2nd) part of 

duodenum• Can cause obstruction, but can also be asymptomatic

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Case Presentation

 A newborn infant was born with a light gray, shiny

mass measuring the size of an orange and

protruding from the umbilical region. It wascovered with a thin transparent membrane.

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Omphalocele

Case Presentation

 A newborn infant was born with a light gray, shiny

mass measuring the size of an orange and

protruding from the umbilical region. It wascovered with a thin transparent membrane.

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Gut Rotation

• Midgut elongates faster than trunk: herniates into umbilical cord in 6th week• Midgut loop connected to yolk sac via a yolk stalk

• Cranial limb of loop: jejunum and most of ileum

• Caudal limb: distal ileum, cecum, ascending colon, proximal part of transverse colon

• Series of three 90º counterclockwise rotations around the superior mesenteric artery

• Sequential return of the gut to the trunk

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Meckel’s (Ileal) Diverticulum

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Congenital Omphalocele

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 Anomalies Associated with Malrotation

nonrotation mixed rotation w/ volvulus reversed rotation

subhepatic cecum & appendix internal hernia midgut volvulus

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ReferencesReferences

• Moore, K. L. 1988. Clinically Oriented Anatomy, 4th Ed. Lippincott, Williams & Wilkins,

Baltimore.

• Moore, K. L. and A. F. Dalley. 1999. Clinically Oriented Anatomy, 6th Ed. Lippincott,

Williams & Wilkins, Baltimore.