Feb 26 M1-Embryology Liver, Pancreas and Portal system Flashcards

1
Q

important thing in gut through development

A

apoptosis cranial t ocaudal (recanalization)

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2
Q

3 main events of gut dev

A
  1. stomach rotation
  2. midgut umb herniation: cecum and appendix counterclockwise rotation
  3. abdominal counterclockwise rotation
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3
Q

2 mechanisms important for recanalization

A
  • genetic

- vascular

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4
Q

fatal failure of apoptosis

A

in biliary tree

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5
Q

main duodenal congenital anomalies

A
  • duodenal atresia (distal to major duod papilla)
  • duodenal stenosis (distal to major duod papilla)
  • intussusception
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6
Q

2 causes for duodenum congenital problems

A

apoptosis failure and bad vascularization (causes failure of apoptosis)

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7
Q

consequence of duod atresia or stenosis

A

polyhyramnios

bilous vomiting in newborn

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8
Q

duod atresia or stenosis on radiograph

A

double bubble sign (air in stomach and in D1 or D2)

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9
Q

main cause for duodenal atresia

A

genetics (associated with trisomy 21) (bad vascularization too leading to failure of apoptosis)

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10
Q

cause for duodenal intussusception

A

poor vascularization.

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11
Q

(IMPORTANT) cause for most anomalies in duodenum vs jejunum and ileum

A

duod: genetics

jejunum + ileum: vascular

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12
Q

ventral and dorsal pancr buds formed where + origin

A

ventral: septum transversum
dorsal: dorsal duodenum
ENDODERMAL in origin

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13
Q

origin of exocrine and endocrine cells of the duodenum

A

endoderm

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14
Q

what distinguishes segments of intestine when it’s forming

A

Hox genes (homeobox genes)

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15
Q

critical hox gene defining whole duodenum AND pancreas later

A

pdx1

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16
Q

where and how pancr buds fuse

A

in clockwise rotation of stomach (foregut rotation). pancreas becomes retroperit

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17
Q

structure that rotates with ventral bud

A

common bile duct (and is placed posterior to D2)

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18
Q

in what bud islets of langerhans form

A

in both

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19
Q

last step of pancreas formation

A

union of the ducts

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20
Q

what dorsal pancreatic bud forms

A

upper head, neck, body tail

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21
Q

what ventral pancreatic bud forms

A

lower head + uncinate process

22
Q

dx sign for duodenum atresia

A

double bubble sign

23
Q

annular pancreas cause

A

ventral bud is a bifid structure and not the whole bifid structure goes around at rotation. some stays with bile system = annular pancreas (ring around duod)

24
Q

annular pancreas dx sign

A

double bubble (+ narrowing on baryum contrast)

25
Q

how portal vein can cause duod obstruction

A

if goes anteriorly instead of posteriorly, pressure on duod bc carries lot of blood

26
Q

(EXAM) what forms the portal system

A

vitelline veins

27
Q

(EXAM) what supplies (vascularization) the gut in embryo

A

vitelline vessels (arteries and veins)

28
Q

(EXAM) what forms drainage of the whole gut

A

vitelline veins

29
Q

structures crossing uncinate process

A

SMA and SMV

30
Q

drainage to the liver before the portal vein was defined (before rotation of ventral bud)

A

2 vitelline veins passing near the 2 pancreatic buds. anastomotic channels between them

31
Q

what determined what formed portal vein

A

vein and anastomotic way that took was the most direct to the liver = portal vein (remained after foregut rotation)

32
Q

problem of anterior portal vein other than duod obstruction

A

get 2 portal veins (quadrate instead of triad) bc splenic vein doesn’t fuse with portal vein

33
Q

midgut position as is in umbilicus

A

proximal midgut to embryo and distal coming back. SMA in between with branches to the 2 parts

34
Q

consequence of umbilical opening too big for midgut

A

anomalies of rotation + anomalies related to lig of treitz and inferior band

35
Q

rotation of midgut

A

in umbilicus. 6-10 wks. 90 counterclockwise

36
Q

2 primitive charact of embryo x section at 8 wks

A
  1. endoderm lining (colonic epith and lumen) with cells apoptosing
  2. walls of colon vs rest of GIT diff in size
37
Q

colon charact at 8 wks + what will form SM

A

has differentiated mesenchyme: will form SM

38
Q

what forms Auerbach’s plexus and Meissner’s plexus

A

NCCs migrating

39
Q

consequence of NCC migration defect

A

megacolon (no Auerbach’s = no peristalsis)

40
Q

cause of umbilica-body wall transitional area

A

lateral folding defects

41
Q

2 types of umbilica-body wall transitional area

A

umb herniation and omphalocele

42
Q

omphalocele def

A

hole too small for grown intestine to reduce back in abdomen. large prominence there at birth

43
Q

umb herniation def

A

intestine reduced but hole too big so went back there

44
Q

lining of umb cord in omphalocele vs umbilical herniation

A

omphalocele = amnion

umb herniation = peritoneum lining

45
Q

omphalocele assoc with what

A

chromosomal abnormalities

46
Q

gastroschisis def

A

intestines go in amniotic cavity (NOT in umb cord) through the body wall on side of umb cord. go through abd wall. split abd wall

47
Q

left and right umb veins in embryo which will be more important

A

left becomes prominent: goes to liver, ductus venosus.

right will regress

48
Q

surface of umbilicus charact

A

surface ectoderm. skin absent (not developed yet). structure is firm

49
Q

region near umb junction to abd wall charact

A

single layer of ectoderm on periphery of that

50
Q

where right umb vein regresses

A

right side of umb junction with abd wall (where single ectoderm layer)

51
Q

gastroschisis cause

A

unknown