Gastroenterology 1 Flashcards
What parts of the GI tract are derived from endoderm?
GI tract epithelium, glands, and many organs that bud off: liver, pancreas, trachea.
What 4 parts of the GI tract are derived from mesoderm?
Connective tissue/strome, muscles, peritoneum, spleen.
The foregut forms which parts of the GI tract?
Celiac trunk, mouth to ampulla of Vater (including liver, gallbladder, bile ducts, pancreas).
The midgut forms which parts of the GI tract?
SMA, ampulla of Vater to transverse colon.
The hindgut forms which parts of the GI tract?
IMA, transverse colon to rectum.
What is mesentery?
Double layer of peritoneum that suspends abdominal organs from cavity walls.
What is the mesentery derived from?
Mesoderm.
Dorsal mesentery covers…
Most abdominal structures.
Ventral mesentery covers…
Exists at the bottom of the esophagus, stomach, and upper duodenum.
What does the liver grow into?
This mesentery forms the lesser omentum and falciform ligament.
The ventral mesentery is derived from?
Septum transversum (mesenchyme tissue).
The Greater omentum hangs from the _______ and is formed from the ________.
Greater curvature of the stomach, mesogastrium.
Where is the lesser omentum and what is it formed from?
Between the liver and stomach, formed from ventral mesentery.
The ‘lung bud’ comes off from what structure?
Foregut.
What structure divides the lung bud from the esophagus?
Tracheoesophageal septum.
Esophageal atresia develops due to…
Abnormal tracheoesophageal septum development; septum deviates posteriorly.
What are 3 clinical features of esophageal atresia?
Polyhydramnios (baby cannot swallow fluid), drooling, choking, vomiting (accumulation secretion), cannot pass NG tube into stomach.
Forms of Esophageal atresia?
EA with tracheoesophageal fistula (TEF): most common, pure EA, H-Type: esophagus and trachea connected by a fistula.
What are 2 clinical findings in a patient with tracheoesophageal fistula?
Gastric distension (air in stomach on CXR), reflux → aspiration pneumonia → respiratory distress.
What is the treatment/prognosis for esophageal atresia?
Treatment: Surgical repair. Prognosis: sometimes residual dysmotility, GERD.
The midgut begins development during which week of gestation?
6th.
Describe the development of the midgut.
Abdomen is too small so intestines herniate through umbilical cord (‘physiologic herniation’ visible on ultrasound!) → midgut rotates around SMA, continues to rotate after return to abdomen by 12th week → results in cecum in right lower quadrant.
What is an omphalocele? What are 2 key features?
Persistence of normal midgut herniation through the umbilicus during development (Normally does not contain liver). Key features: Covered by peritoneum, through umbilical cord.
Liver-containing omphalocele occurs when…
Lateral embryonic folds fail.
What is the clinical presentation of Omphalocele?
Normal GI function BUT associated with other conditions i.e. congenital heart defects (50%), neural tube defects.
What 3 genetic defects are associated with Omphalocele?
Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), Trisomy 13.
What is Gastroschisis? What is a key characteristic?
Extrusion of bowel through abdominal wall due to paraumbilical abdominal wall defect (usually on right side). NOT covered by peritoneum.
What is the clinical presentation of Gastroschisis?
Poor GI function, often associated with atresia, stenosis. Few associated defects → good prognosis if GI function is restored.
What is the treatment for Gastroschisis?
Surgical reduction/closure.
What are 3 possible outcomes of midgut malrotation during development?
Obstruction: Cecum can end up in mid-upper abdomen → stretches peritoneum forming Ladd bands → duodenal obstruction. Volvulus: small bowel twists around SMA → Vascular compromise → ischemia → obstruction. Left sided colon: anatomic variant.
What are the symptoms and treatment for Volvulus?
Symptoms: Vomiting, sepsis, abdominal distension. Treatment: urgent surgery.
Omphalocele vs Gastroschisis
Omphalocele: covered by peritoneum, through umbilical cord. Gastroschisis: not covered by peritoneum, extrusion of bowel.
What is the most common congenital GI abnormality?
Meckel’s Diverticulum.
By week 5, the yolk sac begins to ____ and becomes the ____
Narrow, ‘Yolk stalk,’ ‘vitelline duct,’ ‘omphalomesenteric duct.’
Vitelline duct normally disappears by which week of gestation? Persistence can lead to what?
9th week. Persistence can lead to: Meckel’s diverticulum (most common), cysts/polyps, sinus: cavity behind umbilicus, intestinal discharge from umbilicus.
What is a Meckel’s Diverticulum?
Persistent remnant of vitelline duct, diverticulum of the ileum. Involves all layers of the small bowel (mucosa, submucosa, muscular) → ‘true diverticulum.’
Meckel’s Diverticulum often contains what tissue?
‘Ectopic gastric tissue’, sometimes pancreatic tissue also.
What are the symptoms of Meckel’s Diverticulum? What are 3 possible complications?
Usually no symptoms. Complications: Gastric tissue can secrete acid → ulceration, bleeding; obstruction; diverticulitis.
What is the Meckel’s Diverticulum ‘Rule of 2s’?
2 percent of population, male-to-female ratio 2:1, within 2 feet from ileocecal valve, usually 2 inches in size.
What are 2 ways to diagnose Meckel’s diverticulum?
Technetium scan: Tracer taken up by gastric cells in diverticulum. Capsule endoscopy.
When do Meckel’s diverticulum commonly present?
In childhood.
What is the treatment for Meckel’s diverticulum?
Surgery.
Where is the most common and least common site of atresia/stenosis in the GI tract?
Most common: duodenum. Least common: colon.
What are 2 common symptoms seen in GI atresia and stenosis at birth?
Polyhydramnios, bilious vomiting.
Duodenal Atresia occurs probably due to failure of…
‘Recanalization.’
Duodenal Atresia is associated with what condition?
Down syndrome.
What sign on imaging is seen with Duodenal Atresia?
Double bubble sign (Distention of duodenum stump and stomach with tight pylorus in middle).
What is the mechanism of Jejunal-Ileal-Colonic Atresia?
Vascular disruption → ischemic necrosis of intestine → necrotic tissue is reabsorbed and leaves blind ends of bowel.
In Jejunal-Ileal-Colonic Atresia, the bowel distal to the blind end may be…
Curled → ‘Apple tree atresia.’
Newborns with Pyloric stenosis will present with [2]
‘Projectile,’ non-bilious vomiting; palpable mass (Feels like ‘olive’).
Pyloric stenosis is more common in [M/F]. 30% are [1st/2nd] born children.
Males, 1st.