Digestive System Embryology
Digestive System Embryology
Digestive System Embryology
SYSTEM
The Digestive System
•The primitive gut forms during the 4th week as a
result of head, tail and lateral folding of the embryo.
•The endoderm lined cavity is incorporated into
the embryo, while the yolk sac and the allantois
remain temporarily outside the embryo.
• During folding, somatic mesoderm is attached to
the body wall to give rise to the parietal
peritoneum.
• The mesoderm immediately associated with the
endodermal tube also contributes to most of the
wall of the gut tube.
The Digestive System
• Germ layer contributions:
– endoderm: gives rise to the epithelium and glands of
the digestive tract; mucosal epithelium, mucosal
glands, and submucosal glands.
– mesoderm: gives rise to muscular and fibrous
elements; lamina propria, muscularis mucosae,
submucosa and blood vessels, muscularis externa, and
adventitia/serosa
– neural crest: gives rise to neurons and nerves of the
submucosal plexus and myenteric plexus
• The epithelium at the cranial and caudal ends of the
digestive tract is derived from the ectoderm of the
stomodeum and the proctodeum (anal pit).
The Digestive System
Primitive gut divisions
• Foregut- from oropharyngeal membrane to anterior
intestinal portal
• Midgut – anterior intestinal portal to the posterior
intestinal portal.
• Hindgut: extends from the posterior intestinal
portal to cloacal membrane
• Further folding and growth of the embryo
causes the communication of the gut with the
yolk sac to continue to get smaller and the
foregut, midgut, and hindgut to become
further defined
• Splanchnic mesoderm envelopes
the endodermal lined gut tube and
forms a dorsal mesentery.
• Foregut, midgut and the hind gut
are suspended from the abdominal
wall by the dorsal mesentery.
• The septum transversum forms a
ventral mesentery in the midline
from the diaphragm and anterior
abdominal wall to the umbilicus.
• The ventral mesentry- exists only in
the region of the terminal part of
the esophagus, the stomach, and
upper duodenum.
4th week 5th week
Gall bladder
· Ascending Colon
rectum
· Liver · 2/3 of transverse
colon (variable)
· Pancreas
The Digestive System
10 weeks
11 weeks
Midgut development
caudal limb: terminal part of ileum, caecum,
vermiform appendix, 2/3 transverse colon
Ascending colon develops from the segment of the
midgut loop distal to the caecal bud.
The right 2/3rd of the transverse colon develop
from the postarterial segment of the midgut
loop.
Development of the hindgut
• As the midgut loop returns to the abdominal
cavity, the hindgut swings on its dorsal
mesocolon across to the left.
• The mesocolon fuses with the parietal
peritoneum of the left paravertebral gutter
• At the pelvic brim fusion is incomplete and
part of the dorsal mesocolon remains free as
the sigmoid mesocolon.
Development of the hindgut
• The allantois appears at about 16 days as
a small diverticulum projecting from the
caudal end of the yolk sac into the
connecting stalk
• The urorectal septum, a transverse ridge,
separates the hindgut from the allantois.
It grows towards the cloacal membrane. It
allantois
is derived from mesoderm at the junction
between the connecting stalk and yolk
sac.
• 26 days: After formation of the tail fold,
the allantois and hind gut open into a
common chamber the cloaca.
• The cloacal membrane separates cloaca
from the proctodaeum.
Development of hindgut
• During the 7th week the cloacal
membrane disappears, exposing a
ventral urogenital sinus opening
and a dorsal anal opening.
• The tip of the urorectal septum,
separating the two openings forms
the perineal body.
• The urorectal septum grows
towards the cloacal membrane but
does not fuse with it. It is derived
from mesoderm at the junction Urogenital sinus
Anal opening
between the connecting stalk and
yolk sac. urorectal septum
Development of the hindgut
The Anal Canal
•At the end of the 8th week, after
rupture of the cloacal membrane,
proliferation of ectoderm
occludes the anal opening.
•During the 9th week the opening is
recanalized.
•The terminal part of the anal
canal is ectodermal in origin and
supplied by the inferior rectal
artery.
•The junction between ectoderm
and endoderm is the pectinate
line.
Partition of cloaca
FIXATION OF THE GUT
• At first all parts of the small and large intestines have a
mesentery by which they are suspended from the posterior
abdominal wall.
• After rotation and continued growth of the gut, the
duodenum, the ascending colon, the descending colon and
the rectum become retroperitoneal (by fusion of their
mesenteries with the posterior abdominal wall).
• The original midgut mesentery persists as: the mesentery of
small intestine, and the transverse mesocolon .
• Fixation of the hindgut: when the mesentery fuses with the
peritoneum of the left dorsal abdominal wall and then
disappears posteriorly, the descending colon becomes
retroperitoneal
– THE MESENTERY OF THE SIGMOID COLON, however, persists,
although diminished
CONGENITAL OBSTRUCTION
• This may be due to a variety of causes.
• Atresia (interference with continuity of the lumen;
a segment of the gut may be missing, replaced by
fibrous tissue, or by a septum blocking the lumen
• Stenosis (abnormal narrowing) .
-Abnormal thickening of muscular wall (congenital
pyloric stenosis)
- External pressure by abnormal band or abnormal
blood vessels (bands seen in relation to the
duodenum or compressed by annular pancreas)
• Imperforate anus (caused by stenosis or atresia of
the lower part of the rectum or anal canal).
atresia or stenosis of digestive tract: caused by
failure of recanalization or improper
recanalization, mostly in esophagus and
duodenum
Congenital defects of the stomach
84
congenital malformations of the
digestive tract
• abnormal communication or fistula: Fistula is an
abnormal communication with other cavities or with
the surface of the body. Fistulae are most frequently
seen in relation to the oesophagus and the rectum and
usually associated with atresia of the normal passage.
• duplication
Varying length of the intestinal tract may be
duplicated. The duplication may form only a small cyst,
Or may be of considerable length. It may or may not
communicate with the rest of the intestine.
congenital malformations of the digestive tract
100
---rectal atresia: due to a failure of the anal pit to
develop or deviation of the urorectal septum in
dorsal direction
---rectal fistula: associate with an imperforate anus,
between the rectum and the vagina or urinary
bladder or urethra
imperforate anus, rectal atresia and rectal
fistula:
---imperforate anus: results from failure to
rupture of the anal membrane
肛門會陰瘻管
直腸陰道瘻管
直腸尿道瘻管
THE END