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14 Cards in this Set

  • Front
  • Back

Normal gastrointestinal embryology

1- Foregut 1- Esophagus to duodenum at the level of the pancreatic duct and common bile duct (Ampulla of cater)


2- Midgut - Lower duodenum to proximal 2/3 of transverse colon


3- Hindgut - Distal 1/3 of transverse colon to anal canal above pectinate line

Midgut development

1- 6th week - Physiological hernia took of midgut through umbilical ring


2- 10th week - Returngzhfjf to abdominal cavity and rotate around superior mesenteric artery (SMA)


2- Total 270• counterclockwise

Ventral wall defect

Developmental defect due to failure of rostal fold closure (eg sternal defects (ectopic cordis) lateral fold closure (Omphalocele, gastroschisis) and caudal fold closure (eg bladder e trophy)

Gastroschisis

1- Extrusion of abdominal contents through abdominal fold (right of umbilicus)


2- Not covered by peritoneum or amnion


3- Not associated with congenital anomalies, favorable prognosis

Omphalocele

1- Failure of lateral wall to migrate at umbilical ring- persistent midline herniation of abdominal content into umbilical cord


2- Surrounded by peritoneum


3- Associated with congenital anomalies (trisomy 13, 18 and Beckwith- Wiedmann syndrome) and structural abnormalities (cardiac, GU and neural tube)

Congenital umbilical hernia

1- Failure of closure of umbilical ring after physiology herniation of the midgut


2- Small defects close spontaneously

What congenital disorders are associated with a congenital umbilical hernia

Down syndrome


Congenital hypothyroidism

Tracheoesophageal anamolies

1- Esophalgeal atresia (EA) with distal treacheoesophageal fistual (TEF) most common 85% often present with polyhydromnios in utero (due to inability of fetus to swallow amniotic fluid)


2- Features 1- Neonate drool choke or vomit with fist feed


3- TEF allows air to enter stomach (visible on CXR) - burning with vomit


4- Cyanosis 2’ to laryngospasms (to avoid reflux related aspiration)


5- Clinical test 1- Failure to pass NGT


6- In H type (pure TEF), fistual resemble the letter H


7- In pure EA, CXR shoe gassless abdomen

Intestinal atresia

1- Present with bilious vomiting and abdominal distention with 1-2 days of life


2- Duodenal atresia 1- Failure to recanalize


2- Abdominal X ray shows double bubble sign (dilated stomach and proximal duodenum)


2- Associated with Down’s syndrome


3- Jejunal and ileal atresia 1- Disruption of mesenteric vessels (SMA)


2- Ischemic necrosis of fetal intention— segmental resorption- bowl become discontinuous


3- X ray dilated loops of small bowel with air fluid levels (Triple bubble)

Hypertrophic pyloric stenosis

1- Most common cause of gastric outlet obstruction in infants (1:600)


2- Features 1- Palpable olive shaped mass in epigastric region


2- Visible peristalsis wave


3- Non- bilious projectile vomiting at 2-6 weeks old


3- More common in first born males, associated with exposure to macrolide


4- Results in hypokalmeic hypochloremic metabolic alkalosis (2’ to vomiting gastric acid and volume contraction)


5- U/S - thicken and lengthen pylorus


6- Treatment 1- Surgical resection of pylorus muscle ( pylorumyotomy)

Pancreases embryology

1- Derived from foregut


2- Ventral pancreatic bud contributes to uncinate process and main pancreatic duct


3- Dorsal pancreatic bud contributes to body, tail, isthmus and accessory pancreatic duct


4- Both the ventral and dorsal pancreatic bud contributes to the head

Annular pancreas

1- Abnormal rotation of the ventral pancreatic but form a ring of pancreatic tissue


2- Encircles the 2nd part of the duodenum


3- May cause duodenal narrow and vomiting

Pancreases divisum

1- Failure of the ventral and dorsal pancreatic bud to fuse at 8 weeks


2- Common anomaly


3- Asymptomatic but can cause chronic abdominal pain and/pancreatitis

Spleen embryology

1- Arises in mesentery of the stomach (hence is mesodermal)


2- Foregut blood supply (celiac trunk- splenic artery)