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WEEK 1:

Embryology of abdominal viscera 1:

QuestionAnswer
when does the primitive gut tube form when dorsal part of yolk sac is incorporated into the embryo due to folding of the embryo
where does the primitive gut tube span oropharyngeal membrane to the cloacal membrane
where are the mucosal lining and glands derived from in the primitive gut endoderm (everything else are mesodermal derivatives)
what happens to the epithelial lining of the gut during early development proliferates rapidly and partly or completely obliterates the lumen and the resultant solid-mass gut tube gets recanalized later
folding of embryo takes place during 4th week
what happens at the 4th week embryo folds turning it from flat disc into three dimensional shape
where does folding of embryo occur all around periphery of embryonic disc (longitudinal and transverse)
flat region of endoderm is modified into deep tube to become the primordial foregut
where does the embryo fold from head (longitudinal/ cephalocaudal folding)
what happens at end of 4th week visceral mesoderm layers are continuous with parietal layers as a double layered membrane (dorsal mesentery)
where does the dorsal mesentery extend from caudal limit of foregut to end of hindgut
internalised yolk sac becomes primitive gut
how are the foregut, midgut, and hindgut made during folding the longitudinal plane, part of the yolk sac is pinched off and remains within the embryo
celiac artery supplies foregut (distal oesophagus, stomach, and superior half of duodenum)
superior mesenteric artery supplies midgut (inferior half of the duodenum, ileum, jejunum, caecum, appendix, ascending colon and 'half transverse colon')
inferior mesenteric artery supplies hindgut (rest of the transverse colon, descending and sigmoid colon, rectum, and upper 2/3 of the anal canal)
where does the stomach lie at week 4 in the midline with a body cavity on either side
how is the stomach joined to the body wall via both a ventral and dorsal mesentery
where does the ventral mesentery end more caudally
what type of mesentery does the midgut/ hindgut have dorsal
another name for the dorsal mesentery of the embryonic foregut dorsal mesogastrium
describe the growth of the liver bud grows as an outpouching from the developing duodenum into the ventral mesentery
what is the liver bud composed of gall bladder, system of bile ducts, and ventral part of the pancreas
describe the growth of the dorsal part of the pancreas grows as a similar outpouching as liver bud into the dorsal mesentery
describe the growth of the ventral part of the pancreas grows as an outpouching from the bile duct
describe the growth of the gall bladder (and cystic duct) another bud coming from the bile duct, with the stalk becoming the cystic duct
describe the growth of the right and left hepatic ducts the bile duct divides into the right and left hepatic ducts and these develop into the lobes of the liver, remainder of duct system, and hepatocytes of the liver
which part is the greater part of the pancreas dorsal pancreas
explain what happens due to the differential growth of the duodenum the ventral pancreas and bile duct are displaced behind (posterior) the duodenum, next to the dorsal pancreas and later fuse together
what does the ventral pancreas become uncinate process of the pancreas
what does the dorsal pancreas become head, neck, body, and tail of pancreas
describe the formation of the main pancreatic duct during fusion, most of the original dorsal pancreatic duct joins the ventral pancreatic duct
describe the formation of the accessory pancreatic duct remaining dorsal pancreatic duct becomes the accessory pancreatic duct
biliary atresia failure of main bile duct to form a lumen which progressively leads to deepening jaundice after birth
function of cystic duct connects the gall bladder to common bile duct to transport bile
what would happen if the gall bladder bud does not form during development gall bladder and cystic duct does not form
congenital abnormalities that could occur with the liver gall bladder bud does not form so gall bladder and cystic duct does not form, congenital absence of only the cystic duct so gall bladder opens directly into common hepatic duct , biliary atresia, and annular pancreas
what is a treatment/ management for biliary atresia early surgery, which is critically important to avoid eventual liver failure
annular pancreas occurs when ventral pancreas grows around both sides of gut (around duodenum) which leads to duodenal stenosis
what happens to the stomach during the 4th to 6th week stomach rotates so that its left side becomes its anterior surface
the rotation of the stomach causes what twists the ventral and dorsal mesenteries so that the liver develops on the right and the spleen on the left, helps to pull the duodenum into a 'C' shape, carries duodenum and pancreas against posterior abdominal wall making them (retroperitoneal)
the bare area of liver (no peritoneum covering it) results from direct contact with septum transversum
development of liver divides the ventral mesentery into falciform ligament in front and lesser omentum behind
development of spleen divides the dorsal mesentery into gastrosplenic ligament and splenorenal ligament
how does the greater omentum form from the elongation of the dorsal mesogastrium, which forms the floor of the lesser sac behind the stomach (and hangs down in front of inestines)
how does the midgut communication with the yolk sac via vitelline duct
where is the midgut development suspended from the dorsal abdominal wall
describe the speed of the midgut development and what it leads to rapid elongation creates the primary intestinal loop
describe the rotation of the midgut loop has a 270* counterclockwise rotation around the superior mesenteric artery and elongation of small intestines loop forms the jejunum and ileum as coiled loops
atresia meaning absence of lumen
stenoses meaning narrowing of lumen
congenital abnormalities of GIT atresias, stenoses, abnormal rotations, anterior abdominal wall defects, malrotation eg situs inversus (organs are a mirror image/ flipped on the other side)
the commonest form of congenital duodenal stenosis is due to failure of duodenum to become recanalized (typically occurring caudal to opening of bile duct and is cause of early persistent bile-stained vomiting in the neonate)
gastroschisis congenital fissure in wall of abdomen which DOES NOT INVOLVE UMBILICUS meaning abdominal contents can spill through this defect
omphalocoele congenital hernia in which the abdominal contents protrude into the umbilical cord and is usually associated with other defects
duplications of GIT** abnormal extra segment of GIT developing alongside normal bowel (usually in ileum) which can cause intestinal obstruction, become infected, bleed, cause abdominal pain etc
Meckel diverticulum** congenital pouch arising from ileum due to persistence of vitelline duct (does not disappear) which could lead to bleeding
malformations of the anus and rectum (ARMs)** occurs when developing terminal intestine and anus do not form or separate normally eg normal anal opening is absent or blocked or rectum develops abnormal connection with urethra/vagina
aganglionosis (Hirschsprung disease)** congenital disorder where segment of bowel lacks enteric ganglion cells leading to no normal enteric nervous system and failure of relaxation so bowel remains contracted creating obstruction and bowel contents accumulate above it (constipation, vomiting)
superior mesenteric artery (SMA) syndrome** results from compression of third part of duodenum between SMA and abdominal aorta (where fat usually separates them, fat pad can be reduced leading to less cushioning) leading to post-meal abdominal pain, nausea, and vomiting etc due to low body weight
Created by: 22tango
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