Development Flashcards

1
Q

Foregut area

A

Anything in the digestive tract before the middle of the duodenum

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2
Q

Midgut area

A

Distal 1/2 of duodenum to last 1/3 of transverse colon

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3
Q

Hindgut area

A

Distal 1/3 of transverse colon to last 1/3 of anal canal

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4
Q

Lateral folding of the embryo

A

2D structure of 3 layers (ectoderm, mesoderm and endoderm) forms a cylinder
The ectoderm and mesoderm fold laterally and ventrally which closes off the endoderm forming a separated gut tube structure
The endoderm forms the epithelial lining of the tube
The mesoderm gives rise to the supporting structures and smooth muscle
The outer mesenchymal ayer gives rise to the outer tissue layer
The space in between the mesoderm is the body cavity

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5
Q

Longitudinal folding

A

3D structure bends over to form the foetal position
At about 17 days the opening of the gut tube closes like a purse string, dividing into foregut and hindgut. The midgut remains open to the yolk sac
Further folding causes communication with yolk sac to get smaller and the 3 gut regions become more refined

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6
Q

2 membranes closing off the tube

A

Oropharyngeal membrane at the cranial end

Anal membrane at the caudal end

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7
Q

Key embryonic event at week 4

A

Oropharyngeal membrane ruptures

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8
Q

Key embryonic event at week 8

A

Anal membrane ruptures

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9
Q

Lumen of the gut tube

A

Initially the gut tube is patent. As epithelium proliferates the lumen of the gut tube is plugged up. During week 8, recanalisation occurs

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10
Q

The foregut receives blood from:

A

The coeliac trunk

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11
Q

The midgut receives blood from:

A

The superior mesenteric artery

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12
Q

The hindgut receives blood from:

A

The inferior mesenteric artery

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13
Q

Tracheoesophageal fistula/atresia

A

Fistula: connection
Atresia: blockage
Both occur as a result of incomplete partitioning

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14
Q

Congenital hiatal hernia

A

Short oesophagus

Displaces stomach cranially and herniates into thorax through oesophageal hiatus

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15
Q

Dilation and rotation of stomach

A

Gut tube starts to dilate and continues through the rotations
Rotation of tube on long axis 90° clockwise. Anterior mesogastrium moves to the right and posterior mesogastrium moves to the left.
Then, rotation of tube on coronal axis 90° clockwise. Right boundary becomes superior (lesser curvature) and left boundary becomes inferior (greater curvature)

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16
Q

Formation of greater omentum

A

As dorsal mesogastrium is dragged round by rotation of stomach it hangs down under the weight of gravity. Both sides of the hanging fold fuse together making a 4 layered peritoneal structure, the greater omentum.

17
Q

Congenital hypertrophic pyloric stenosis

A

Marked thickening of the muscular wall of the pylorus, blocking exit of the stomach into the duodenum

18
Q

Hepatic diverticulum

A

Outgrowth of the duodenum at week 4 of development forming the liver and biliary apparatus

19
Q

Pancreas development

A

Develops between both layers of mesogastrium

Ventral and dorsal bud: eventually anastamose forming a pancreatic duct

20
Q

Midgut herniation

A

Normal process where loop migrates through into umbilical cord. Eventually this herniation retracts and the loop returns to the abdominal cavity

21
Q

Abnormal midgut rotations

A
Non-rotation
Twisting
Reversed rotation
Sub-hepatic caecum and appendix (failure to descend)
Internal hernia
Midgut volvulus (obstructs duodenum)
22
Q

Umbilical herniation or fistula

A

Failure of umbilical cord to close properly. Gut herniates through weak region in the body wall

23
Q

Meckels diverticulum

A

Ileal diverticulum

Remnant of the vitelline duct

24
Q

Cloaca

A

Expanded distal part of hindgut divided into dorsal and ventral parts

25
Q

Mesenchymal urorectal septum

A

As septum grows it separates rectum from urogenital sinus

26
Q

Rectum/anal canal

A

Boundary between outer ectoderm and inner endoderm

Inferior mesenteric artery supplies upper 2/3

27
Q

Anocutaneous line

A

Portion of the anal canal where the lymphatics change. Below this line superficial inguinal nodes are found

28
Q

Hirschsprungs disease

A

Segment of colon is dilated due to absence of ANS ganglion cells in distal gut wall
Peristalsis failure in aganglionic part means the colon can’t relax which prevents movement of intestinal contents

29
Q

Imperforated anus

A

Failure of anal membrane to perforate

30
Q

Rectal atresia

A

Anal canal and rectum are separated

Fistulas may present which can connect intestine to urethra, bladder or vagina