Development 2 Flashcards

1
Q

What does teh midgut give rise to (twisting - can lead to duodenal obstructing, compression fo blood supple, ishacemia)

A
• Gives rise to:
– Small intestine, including most of duodenum 
– Caecum &  appendix 
– Ascending colon 
– Proximal 2/3 transverse colon
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2
Q

What happens to the primary intestinal loop

A
• The midgut elongates
enormously 
• Runs out of space
– Makes a loop that
• has the SMA as its axis
• is connected to the yolk sac by the vitelline duct (part of same tube)
• has cranial & caudal limbs
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3
Q

What happens to the intestinal loop in the 6th week

A

• During 6th week, growth of the primary intestinal loop is very rapid
– elongation
• Liver is also growing rapidly
– abdominal cavity is too small to accommodate both
• Intestines herniate into the umbilical cord

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4
Q

Give an overview of midgut rotation

A

3x 90 degree turns
Continuing extension in length of small intestine
Cranial alove, then 90 turn, now Uber’s lie side by side. Another turn, and caudal limb at head end. As it returns to the cavity, another 90 degree turn
This meas that
cranial limb returns to abdominal cavity first, moving to the left side
Crackle bud grows. This grows down to create caecum and ascending colon
See slide

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5
Q

Give 2 examples of malrotation

A

• Incomplete rotation
– Midgut loop makes only one
90° rotation
• Left-sided colon bc caudal limb went back in first

• Reversed rotation
– Midgut loop makes one 90°
rotation clockwise
• Transverse colon passes
posterior to the duodenum
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6
Q

What are the risks associated with midgut defects

A

• Most complications present in the neonatal period
• Volvulus
– Strangulation, compression of blood supply,
– Ischaemia

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7
Q

What is volvulus

A

(twisting - can lead to duodenal obstructing, compression fo blood supple, ishacemia)

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8
Q

Describes some abnormalities in terms fo remnants of the yolk stalk

A

The vitelline duct can persist resulting a number of different abnormalities

vitelline cyst - Vitelline duct forms fibrous strands - fluid filled cyst in a fibrous cord
Vitelline fistula - Not lost the intel line duct - havent resolved communication between midgut and umbillicus - direct communication between them
meckels diverticulitis - remnant of yolk stalk - AKA ileal diverticulum, the most common GI anomaly

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9
Q

What is meckels diverticulum

A

AKA ileal diverticulum, the most common GI anomaly
• Rule of 2s
• 2% population
• 2 feet from ileocaecal valve
• Usually detected in under 2s
• 2:1 ration male:female
• Can contain ectopic gastric or pancreatic tissue

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10
Q

Why does recanlisation occur and where

A

• The primitive gut is a simple tube
• In some gut structures, cell growth becomes so rapid that the lumen is
partially or completely obliterated
– oesophagus, bile duct, small intestine • Recanalisation occurs to restore the lumen
• If recanalisation is wholly or partially unsuccessful, atresia or stenosis of the
structure can occur

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11
Q

What are atresia and stenosis

A

• Atresia
– Lumen obliterated
• Stenosis
– Lumen narrowed - limit passage but not completely blocked

• Most occur in duodenum
– Most likely cause is incomplete canalisation
– But “vascular accidents” may also contribute eg olvulus etc

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12
Q

What is pyloric stenosis

A
• Pyloric stenosis
– hypertrophy of the circular smooth muscle in the region of the pyloric sphincter 
– NOT a recanalisation failure
• Common abnormality of the stomach
in infants
– narrowing of the exit from the
stomach causes characteristic
projectile vomiting
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13
Q

What is gastrochisis

A
• Failure of closure of the abdominal
wall during folding of the embryo 
• Leaves gut tube & derivatives outside
the body cavitiy
Relatively easy to correct
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14
Q

What is omplalocoele

A

• a.k.a. exomphalos
– Persistence of physiological herniation
– Differs from umbilical hernia because hernias have covering of skin and subcut. tissue
– i.e. in hernia, gut had completed physiological herniation sequence, but omphalocoele doesnt - major fundamental problem with development
Problem with development - has a spectrum of other structural defects

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15
Q

Wha does the hindgutgive rise to

A
• Gives rise to
– Distal 1/3 transverse colon
– Descending colon
– Rectum
– Superior part of anal canal
– Epithelium of urinary bladder
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16
Q

Describe the development of he anal canal

A
The anal canal is divided by the pectinate line into histologically
distinct superior and inferior parts
– indicates differences in arterial
supply, venous & lymphatic
drainage and innervation
17
Q

What os the proctoderm

A
Junction between two embryonic
germ layers
Junction between two embryonic
germ layers
See slide
18
Q

Compare above and below the pectinate life

A
Above pectinate line - visceral  
– IMA
– S2,3 & 4 pelvic parasympathetics
– Columnar epithelium
– Lymph. drainage = internal iliac 
• Below pectinate line - somatic
– Pudendal A
– S2,3 & 4 pudendal N
– Stratified epithelium
– Lymph. drainage = superficial nodes
inguinal nodes

Contribution of two embryonic tissues to the anal canal means that …..
above the pectinate line the only sensation possible is stretch,
while below the pectinate line the tissue is temperature, touch and pain sensitive

19
Q

Describe visceral pain

A
  • Visceral pain poorly localised
  • The pattern reflects the development of the structure
  • Foregut & its derivatives – epigastrium
  • Midgut – periumbilical
  • Hindgut – suprapubic
20
Q

What are some hindgut abnormalities

A

• Imperforate anus
– Failure of anal membrane to rupture
• Anal / anorectal agenesis
• Hindgut fistulae - abjormal communication eg between hindgut and bladder

21
Q

Which structures retain mesenteries

A
Mesenteries are retained by:
– Jejunum
– Ileum
– Appendix
– Transverse colon
– Sigmoid colon
22
Q

Which structures have used mesenteries

A
Structures of midgut/hindgut with
fused mesenteries:
– Duodenum
– Ascending colon
– Descending colon
– Rectum (no peritoneal covering in
distal 1/3)