GIT-Anatomy Flashcards
Tongue development?
1. Ant 2/3 = Pharyngeal arch-1st 2. Post 1/3 = Pharyngeal arch -3rd & 4th 3.
Normal GastroIntestinal Embryology ?
Foregut—esophagus to duodenum at level of pancreatic duct and common bile duct insertion (ampulla of Vater). 4th-6th week of development—stomach rotates 90° clockwise. Left vagus becomes anteriorly positioned, and right vagus becomes posteriorly positioned. Midgut—lower duodenum to proximal 2/3 of transverse colon. 6th week of development—physiologic herniation of midgut through umbilical ring. 10th week of development—returns to abdominal cavity rotating around superior mesenteric artery (SMA), 270° counterclockwise (~180° before 10th week, remaining ~90° in 10th week). Hindgut—distal 1/3 of transverse colon to anal canal above pectinate line
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Ventral wall defects
1. Omphalocele 2. Gastroschisis
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Gastroschisis??
1. Paraumbilical herniation of abdominal contents through abdominal wall defect 2.Not covered by peritoneum or amnion A ; “the guts come out of the gap (schism) in the letter G” 3.Not associated with chromosome abnormalities; good prognosis
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Omphalocele ?
1. Herniation of abdominal contents through umbilicus 2.Covered by peritoneum and amnion 3.Associated with congenital “Onomalies” (eg, trisomies 13 and 18, Beckwith-Wiedemann syndrome) and other structural abnormalities (eg, cardiac, GU, neural tube)
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Congenital umbilical
hernia ?
Failure of umbilical ring to close after physiologic herniation of midgut. Covered by skin C . Protrudes with intra-abdominal pressure (eg, crying). May be associated with congenital disorders (eg, Down syndrome, congenital hypothyroidism). Small defects usually close spontaneously
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Tracheoesophageal
anomalies ?
1. Esophageal atresia (EA) 2. distal tracheoesophageal fistula (TEF) 3. polyhydramnios 4. Gasless abdomen in EA 5. TEF-------H type fistula 6. TEF= Allow air in the stomach seen in CXR 7. Cannot pass Nasogastric tube in stomach
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Hypertrophic pyloric
stenosis ?
1. Pyloric sphincter muscle--Hypertrophy + Hyperplasia 2. Palpable olive mass 3. Most common cause of Gastric Outlet Obstruction 4. Projectile vomiting (2-6) weeks 5. Firstborn male + [Macrolide] 6. Hypokalemia Hypochloremic Metabolic alkalosis 7. Thickened and Lengthened pylorus 8. Tx- surgical incision of pyloric muscle / PYLOROMYOTOMY
Intestinal atresia ?
Presents with bilious vomiting and abdominal distension within first 1–2 days of life. Duodenal atresia—failure to recanalize. X-ray A shows “double bubble” (dilated stomach, proximal duodenum). Associated with Down syndrome
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Jejunal and ileal atresia ?
disruption of mesenteric vessels (typically SMA) ischemic necrosis of fetal intestine segmental resorption: bowel becomes discontinuous. X-ray may show “triple bubble” (dilated stomach, duodenum, proximal jejunum) and gasless colon. Associated with cystic fibrosis and gastroschisis. May be caused by tobacco smoking or use of vasoconstrictive drugs (eg, cocaine) during pregnancy.
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Pancreas and spleen
embryology ?
Pancreas—derived from foregut. Ventral pancreatic bud contributes to uncinate process. Both
ventral and dorsal buds contribute to pancreatic head and main pancreatic duct
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Annular pancreas ?
—abnormal rotation of ventral pancreatic bud forms a ring of pancreatic tissue
encircles 2nd part of duodenum; may cause duodenal narrowing (arrows in A ) and vomiting.
Associated with Down syndrome
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Pancreas divisum ?
ventral and dorsal parts fail to fuse at 7 weeks of development. Common
anomaly; mostly asymptomatic, but may cause chronic abdominal pain and/or pancreatitis``
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Spleen Embryology
Spleen—arises in mesentery of the stomach (dorsal mesogastrium, hence, mesodermal), but has
foregut supply (celiac trunk splenic artery).
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Retroperitoneal
structures ?
SAD PUCKER: Suprarenal (adrenal) glands [not shown] Aorta and IVC Duodenum (2nd through 4th parts) Pancreas (except tail) Ureters [not shown] Colon (descending and ascending) Kidneys Esophagus (thoracic portion) [not shown] Rectum (partially) [not shown]
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