DEVELOPMENT OF GIT
AND MALROTATION
MODERATOR: Dr.K.SAMBASIVA RAO MDRD
HOD AND PROFESSOR
PRESENTER:Dr.SNEHA
PGY1
DEVELOPMENT OF GIT
• EMBRYONIC FOLDING
- Development of gut tube
- Development of peritoneum
• FOREGUT , MIDGUT , HINDGUT
-Components
-Vascular supply
-Mesenteries
• RETROPERITONEAL ORGANS
• MALROTATION
FORMATION OF PRIMITIVE GUT TUBE
• The gut tube is formed from endoderm lining the yolk sac
which is enveloped by the developing coelom as the result
of cranial and caudal folding.
• During folding , somatic mesoderm is applied to the body
wall to give rise to the parietal peritoneum.
• Visceral (splanchnic) mesoderm wraps around the gut tube
to form the mesenteries that suspend the gut tube within
the body cavity.
• The mesoderm immediately associated with the
endodermal tube also contributes to most of the gut tube.
DEFINITIVE SUBDIVISIONS OF THE GUT
TUBE
• Within the abdominal cavity, the gut is definitively divided
into foregut, midgut, and hindgut.
• BASED ON THE ARTERIAL SUPPLY:-
• Foregut derivatives in the abdomen are supplied by
branches of the celiac artery.
• Midgut derivatives are supplied by branches of the superior
mesenteric artery.
• Hindgut derivatives are supplied by branches of the inferior
mesenteric artery.
• As the gut tube develops, the endoderm proliferates rapidly
and actually temporarily occludes the lumen of the tube
around the 5th
week.
• Growth and expansion of mesoderm components in the wall
coupled with apoptosis of some of the endoderm at around
the 7th
week causes recanalization of the tube such that by
the 9th
week , the lumen is open again
• This occlusion and recanalization process occurs throughout
the tube (esophagus to anus) and errors in this process can
occur in anywhere along the tube resulting in stenosis
(narrowing of the lumen or even outright occlusion ) in that
region.
DERIVATIVES OF FOREGUT
• Trachea and respiratory tract
• Lungs
• Esophagus
• Stomach
• Liver gall bladder and bile ducts
• Pancreas (dorsal and ventral)
• Upper duodenum
• Mesentery [dorsal and ventral mesogastrium]
ESOPHAGUS AND TRACHEA:-The region of foregut just
caudal to the pharynx develops two longitudinal ridges
called the tracheoesophageal folds that divide the tube
ventrally into trachea (and subsequent lung buds), and
dorsally into the esophagus.
STOMACH :- It appears as a fusiform dilation of the foregut
endoderm which undergoes a 90 rotation such that the left
◦
side moves ventrally and the right moves dorsally [the vagus
nerve follows this rotation which is how the left vagus
becomes anterior and the right vagus becomes posterior].
-differential growth on the left and right side establishes the
greater and lesser curvatures respectively; craniocaudal
rotation tips the pylorus superiorly
-dorsal and ventral mesenteries of the stomach are
retained to become the greater and lesser omentum.
LIVER:- Arises out of the ventral foregut endoderm adjacent
to septum transversum(the mesoderm of the septum
transversum and developing heart send signals that induce
this region of endoderm to become liver)
- The parenchyma of the liver (cords of hepatocytes and
branched tubules of bile ducts) intercalates within the tissue
of the septum transversum and the plexus of vitelline vessels,
accounting for the overall architecture observed in the adult.
PANCREAS:- The endodermal lining of the foregut forms
two outgrowths caudal to the forming liver : the ventral
pancreatic bud and the dorsal pancreatic bud.
- Within each bud , the endoderm developed into branched
tubules attached to the secondary acini (the exocrine
pancreas)
- The endocrine pancreas (islets of Langerhans) arise from the
stem cells at the duct branch points that then develops into
discrete islands of vascularized endocrine tissue.
- Primary rotation of the gut tube , causes the ventral and
dorsal buds to merge together into what is usually a single
organ in the adult.
- Ventral pancreatic bud-uncinate process of the head
- Dorsal pancreatic bud-remaining portion of the head, body
and tail
PROXIMAL DUODENUM:-
Arises from the caudal most
part of the foregut and is
served by anterior and
posterior branches of the
superior
pancreaticoduodenal artery ,
which is a branch of the celiac
artery.
- With rotation of the gut tube ,
the duodenum and pancreas
are pushed against the body
wall and become secondarily
retroperitoneal.
DERIVATIVES OF MIDGUT
• Lower duodenum
• Jejunum
• Ileum
• Caecum
• Appendix
• Ascending colon
• Proximal transverse 2/3rd
colon
• Mesentery [small bowel mesentery, mesoappendix ,
transverse mesocolon]
DISTAL DUODENUM:- Distal or lower duodenum arises
from the cranial most portion of the midgut and is served
by anterior and posterior branches of the inferior
pancreaticoduodenal artery, branch of SMA.
JEJUNUM, ILEUM PORTION OF LARGE INTESTINE FROM
MIDGUT:- Midgut elongates rapidly beyond the capacity of
the embryonic abdominal cavity and thus forms a u shaped
loop that herniates into the umbilicus and is oriented
parallel to axis of the embryo such that there is an upper or
cranial loop[jejunum and upper pat of ileum] and a lower or
caudal loop.
DERIVATIVES OF HINDGUT
• Distal 1/3rd
transverse colon
• Descending colon
• Sigmoid colon
• Rectum
• Upper anal canal
• Urogenital sinus
• Mesentery [ transverse mesocolon , sigmoid mesocolon]
• Include the distal 1/3rd
of the transverse colon , descending
colon, sigmoid colon , rectum , and upper anal canal.
• Terminal end of the hindgut ends in an endoderm lined
pouch called cloaca , which is in common with the
developing lower urogenital tract.
• The formation of a urorectal septum divides the cloaca
ventrally into urogenital sinus and dorsally into the
rectoanal canal.
• The portion of the cloaca where the hindgut endoderm is up
against the ectoderm of the skin breaks down to allow the
formation of the anus.
RETROPERITONEAL ORGANS
• PRIMARY
1. Abdominal aorta
2. Ivc
3. Adrenals
4. Kidneys
5. Ureters
6. Bladder
7. Lower rectum
8. Esophagus
• SECONDARY
1. 2,3,4 TH PART OF THE DUODENUM
2. ASCENDING COLON
3. DESCENDING COLON
4. HEAD AND BODY OF PANCREAS
These organs connects to the posterior wall through
adventitia.
ANOMALIES OF
MIDGUT
1]OMPHALOCELE
2]GASTROSCHISIS
3]MECKEL DIVERTICULUM
4]MALROTATION
5]DUODENAL ATRESIA/STENOSIS
1]OMPHALOCELE
• A/K/A EXOMPHALOS , are congenital midline abdominal
wall defects at the base of the umbilical cord insertion, with
herniation of gut [or occasionally other structures ] out of
the fetal abdomen.
• USG:- multiple bowel loops (and on occasion liver) herniate
into a membrane-covered defect (i.e. not free-flowing) and
are usually seen as hyperechogenic content (non-fluid filled
bowel)
• the umbilical cord insertion is directly into the omphalocele
• Plain radiograph
• In neonates, radiographs show herniated bowel loops covered by a
membrane.
• CT
• CT, although not routinely used in neonates, permits direct visualization
of herniation content +/- evidence of any malrotation.
• MRI
• as with CT, allows better direct visualization of the herniation through
the abdominal wall
• the herniated liver is often of low T2 signal and the bowel of high T2
signal
THERE IS A LARGE SOFT TISSUE
MASS PROJECTED OVER THE
RIGHT SIDE OF THE ABDOMEN
MIDLINE ABDOMINAL DEFECT WITH
HERNIATION OF ABDOMINAL
CONTENTS
A LARGE MUSCULAR DEFECT
IS SEEN IN THE ANTERIOR WALL
LIVER, GB, STOMACH AND
SOME OF BOWEL LOOPS ARE
PROTRUDED THROUGH THE
DEFECT ANTERIORLY
2]GASTROSCHISIS
• Extra-abdominal herniation of fetal or neonatal bowel loops (and
occasionally portions of the stomach , liver , and/or gall bladder)
into the amniotic cavity through a para-umbilical anterior
abdominal wall defect.
• USG:-The herniated content is towards the right side of the
umbilical cord in most cases; color Doppler may be useful to locate
the cord in relation to the herniation. This causes the fetal
abdominal circumference to be smaller than expected for
gestation age. The herniated bowel often appears free-floating
rather than contained. The herniated bowel wall can be thickened
due to edema.
• There can be either accompanying oligohydramnios or
polyhydramnios as ancillary sonographic sonographic features.
THERE IS HERNIATION OF SMALL BOWEL LOOPS
THROUGH A RIGHT PARAUMBILICAL ABDOMINAL
WALL DEFECT. AIR IS SEEN IN THE STOMACH. THERE
IS NO SOLID ORGAN HERNIATION EVIDENT
THERE IA AN ANTERIOR ABDOMINAL WALL DEFECT
WITH PROTRUSION OF THE BOWEL LOOPS OUT
THE ABDOMINAL CAVITY WITHOUT ANY COVERING
3]MECKEL DIVERTICULUM
• Remnant of the vitelline duct, which connects the yolk sac to the
midgut through the umbilical cord. This duct is typically
obliterated by the 5th
to 8th
week of gestation.
• Fluoroscopy
• Small bowel enemas have sometimes been used for the diagnosis
in some centers, although a precise technique is required if the
diagnosis is to be excluded with any degree of certainty 4
.
• Ultrasound
• Usually of limited use in the diagnosis of an uncomplicated
Meckel diverticulum. Ultrasound may show a blind-ending
peristaltic loop connected to the small bowel - it may have a
multi-layered appearance of the wall.
• CT
• CT is of limited value in uncomplicated cases, as the
diverticulum may resemble a normal bowel loop. CT may
show a fluid- or air-filled blind-ending pouch that arises
from the antimesenteric side of the distal ileum.
• It is possible for the diverticulum to invert and appear as an
intraluminal polypoid lesion 1
FOCAL OUTPOUCHING OF MILDLY DILATED
FECES-FILLED ILEUM , JUST PROXIMAL TO THE
TRANSITION POINT, LIKELY DIVERTICULUM
THERE IS A BLIND ENDING, AIR-FILLED , DISTENDED
TUBULAR/DIVERTICULAR STRUCTURE ORIGINATING
OFF THE DISTAL ILEAL BOWEL WIT THE BASE OF THE
DIVERTICULUM BEAING NARROWED AT ITS ORIGIN.
4]MALROTATION
• In the developing embryo growth of the bowel requires herniation
into the omphalomesenteric sac.
In the tenth week of gestation the bowel returns to the abdominal
cavity.
• This return is accompanied by a counterclockwise rotation of the
midgut to achieve its final position with the ligament of Treitz in the
left upper quadrant and the caecum in the right lower quadrant,
suspended from a long mesentery.
• Malrotation arises when the rotation is arrested or even reversed.
As a result the bowel has an abnormal position, the mesentery is
short and peritoneal bands, called Ladd's bands, may cross from the
caecum to the liver or to the anterior abdominal wall.
• Left
Normal situation with the duodenum
retroperitoneal.
Treitz ligament is on the left side of the spine.
The small intestine is predominantly on the left.
The cecum is in the right lower quadrant
There is a long mesentery.
• Middle
Displacement of Treitz inferiorly and rightward.
The small intestine is found predominantly on
the right.
Fibrous bands course over the vertical portion
of the duodenum causing obstruction.
• Right
Volvulus due to short mesentery. Ischemic
bowel.
• The malrotation will become symptomatic only when a
volvulus occurs due to the short mesentery or when the
Ladd's band obstruct the duodenum
• Both presentations are most common in the neonatal
period.
• However sometimes it can also present later in life, for
example when the volvulus is intermittent or when the
Ladd's bands create relatively little obstruction.
• Acute volvulus is a life-threatening presentation and
requires prompt surgical intervention.
• The upper GI-study shows
a malrotation
complicated by a volvulus.
• This results in the typical
corkscrew or reversed 3
sign.
• An overfilled stomach
could hide the corkscrew
on the AP projection so
the stomach should first
be aspirated by use of a
nasogastric tube and the
volume of injected
contrast should be small.
• Sometimes a malrotation can be suspected when
on ultrasound the superior mesenteric artery is
seen to lie to the right of the superior mesenteric
vein.
• This sign however is neither specific nor sensitive
and should not be used when asked to investigate
for suspected malrotation without a volvulus.
• An abnormal location of ligament of Treitz on an
upper GI series is the gold standard for malrotation.
• In case of a volvulus the child is acutely sick and ultrasound
is often the modality of choice.
• This will show a whirlpool sign of the vessels which confirms
the presence of a volvulus.
• The corkscrew sign of the bowel on the upper GI is
equivalent.
Once a volvulus is diagnosed on ultrasound, the child
should go straight to the operating room and no more time
should be lost on further imaging.
USG showing whirlpool sign of vessels which confirms
the presence of volvulus
14 DAYS MALE BABY OF BHAVANI
5] DUODENAL ATRESIA/STENOSIS
• Duodenal atresia results from a congenital malformation of
the duodenum and requires prompt correction in the
neonatal period. It is considered to be one of the
commonest causes of fetal bowel obstruction.
• Plain radiograph
• Abdominal radiographs may classically show a
double bubble sign with gas filled distended stomach and
duodenum with an absence of distal gas. A similar
appearance (either filled with fluid or gas) can be seen in
other modalities.
• Barium study
• Barium contrast can be
administered sometimes via an
orogastric or nasogastric tube
under fluoroscopy to evaluate
the upper gastrointestinal tract.
Only a controlled amount of
barium is placed to confirm
obstruction. It is then removed
by nasogastric tube to prevent
reflux and potential aspiration.
• Ultrasound
• May also show a dilated stomach and duodenum giving a double
bubble type appearance. This, however, may not be
sonographically detectable until the mid to late second trimester.
May also show evidence of polyhydramnios as an ancillary
sonographic feature.
• If a double-bubble sign is seen on antenatal ultrasound, then it is
important to demonstrate a connection between the two fluid-
filled structures because foregut duplication cyst, as well as other
abdominal cysts, may simulate the appearance of a double-bubble
sign.
• Likewise, a "double bubble" may be seen in cases of Ladd's bands,
annular pancreas or volvulus, in which there is no duodenal
atresia.
Gaseous distension of stomach and
proximal duodenum with absence of
bowel gas distally giving the classical
appearance of double bubble sign,
compatible with duodenal atresia.
Antenatal ultrasound showing increased liquor amnii
(polyhydramnios) with two communicating cystic
structures in upper abdomen of the fetus suggestive
of double bubble sign and representing over
distended fetal stomach and proximal duodenum.
THANK
YOU

DEVELOPMENT_OF_GIT_..................pptx

  • 1.
    DEVELOPMENT OF GIT ANDMALROTATION MODERATOR: Dr.K.SAMBASIVA RAO MDRD HOD AND PROFESSOR PRESENTER:Dr.SNEHA PGY1
  • 2.
    DEVELOPMENT OF GIT •EMBRYONIC FOLDING - Development of gut tube - Development of peritoneum • FOREGUT , MIDGUT , HINDGUT -Components -Vascular supply -Mesenteries • RETROPERITONEAL ORGANS • MALROTATION
  • 3.
    FORMATION OF PRIMITIVEGUT TUBE • The gut tube is formed from endoderm lining the yolk sac which is enveloped by the developing coelom as the result of cranial and caudal folding. • During folding , somatic mesoderm is applied to the body wall to give rise to the parietal peritoneum. • Visceral (splanchnic) mesoderm wraps around the gut tube to form the mesenteries that suspend the gut tube within the body cavity. • The mesoderm immediately associated with the endodermal tube also contributes to most of the gut tube.
  • 7.
    DEFINITIVE SUBDIVISIONS OFTHE GUT TUBE • Within the abdominal cavity, the gut is definitively divided into foregut, midgut, and hindgut. • BASED ON THE ARTERIAL SUPPLY:- • Foregut derivatives in the abdomen are supplied by branches of the celiac artery. • Midgut derivatives are supplied by branches of the superior mesenteric artery. • Hindgut derivatives are supplied by branches of the inferior mesenteric artery.
  • 8.
    • As thegut tube develops, the endoderm proliferates rapidly and actually temporarily occludes the lumen of the tube around the 5th week. • Growth and expansion of mesoderm components in the wall coupled with apoptosis of some of the endoderm at around the 7th week causes recanalization of the tube such that by the 9th week , the lumen is open again • This occlusion and recanalization process occurs throughout the tube (esophagus to anus) and errors in this process can occur in anywhere along the tube resulting in stenosis (narrowing of the lumen or even outright occlusion ) in that region.
  • 11.
    DERIVATIVES OF FOREGUT •Trachea and respiratory tract • Lungs • Esophagus • Stomach • Liver gall bladder and bile ducts • Pancreas (dorsal and ventral) • Upper duodenum • Mesentery [dorsal and ventral mesogastrium]
  • 12.
    ESOPHAGUS AND TRACHEA:-Theregion of foregut just caudal to the pharynx develops two longitudinal ridges called the tracheoesophageal folds that divide the tube ventrally into trachea (and subsequent lung buds), and dorsally into the esophagus. STOMACH :- It appears as a fusiform dilation of the foregut endoderm which undergoes a 90 rotation such that the left ◦ side moves ventrally and the right moves dorsally [the vagus nerve follows this rotation which is how the left vagus becomes anterior and the right vagus becomes posterior].
  • 13.
    -differential growth onthe left and right side establishes the greater and lesser curvatures respectively; craniocaudal rotation tips the pylorus superiorly -dorsal and ventral mesenteries of the stomach are retained to become the greater and lesser omentum.
  • 15.
    LIVER:- Arises outof the ventral foregut endoderm adjacent to septum transversum(the mesoderm of the septum transversum and developing heart send signals that induce this region of endoderm to become liver) - The parenchyma of the liver (cords of hepatocytes and branched tubules of bile ducts) intercalates within the tissue of the septum transversum and the plexus of vitelline vessels, accounting for the overall architecture observed in the adult.
  • 16.
    PANCREAS:- The endodermallining of the foregut forms two outgrowths caudal to the forming liver : the ventral pancreatic bud and the dorsal pancreatic bud. - Within each bud , the endoderm developed into branched tubules attached to the secondary acini (the exocrine pancreas) - The endocrine pancreas (islets of Langerhans) arise from the stem cells at the duct branch points that then develops into discrete islands of vascularized endocrine tissue. - Primary rotation of the gut tube , causes the ventral and dorsal buds to merge together into what is usually a single organ in the adult. - Ventral pancreatic bud-uncinate process of the head - Dorsal pancreatic bud-remaining portion of the head, body and tail
  • 17.
    PROXIMAL DUODENUM:- Arises fromthe caudal most part of the foregut and is served by anterior and posterior branches of the superior pancreaticoduodenal artery , which is a branch of the celiac artery. - With rotation of the gut tube , the duodenum and pancreas are pushed against the body wall and become secondarily retroperitoneal.
  • 20.
    DERIVATIVES OF MIDGUT •Lower duodenum • Jejunum • Ileum • Caecum • Appendix • Ascending colon • Proximal transverse 2/3rd colon • Mesentery [small bowel mesentery, mesoappendix , transverse mesocolon]
  • 21.
    DISTAL DUODENUM:- Distalor lower duodenum arises from the cranial most portion of the midgut and is served by anterior and posterior branches of the inferior pancreaticoduodenal artery, branch of SMA. JEJUNUM, ILEUM PORTION OF LARGE INTESTINE FROM MIDGUT:- Midgut elongates rapidly beyond the capacity of the embryonic abdominal cavity and thus forms a u shaped loop that herniates into the umbilicus and is oriented parallel to axis of the embryo such that there is an upper or cranial loop[jejunum and upper pat of ileum] and a lower or caudal loop.
  • 24.
    DERIVATIVES OF HINDGUT •Distal 1/3rd transverse colon • Descending colon • Sigmoid colon • Rectum • Upper anal canal • Urogenital sinus • Mesentery [ transverse mesocolon , sigmoid mesocolon]
  • 25.
    • Include thedistal 1/3rd of the transverse colon , descending colon, sigmoid colon , rectum , and upper anal canal. • Terminal end of the hindgut ends in an endoderm lined pouch called cloaca , which is in common with the developing lower urogenital tract. • The formation of a urorectal septum divides the cloaca ventrally into urogenital sinus and dorsally into the rectoanal canal. • The portion of the cloaca where the hindgut endoderm is up against the ectoderm of the skin breaks down to allow the formation of the anus.
  • 27.
    RETROPERITONEAL ORGANS • PRIMARY 1.Abdominal aorta 2. Ivc 3. Adrenals 4. Kidneys 5. Ureters 6. Bladder 7. Lower rectum 8. Esophagus
  • 28.
    • SECONDARY 1. 2,3,4TH PART OF THE DUODENUM 2. ASCENDING COLON 3. DESCENDING COLON 4. HEAD AND BODY OF PANCREAS These organs connects to the posterior wall through adventitia.
  • 29.
  • 30.
    1]OMPHALOCELE • A/K/A EXOMPHALOS, are congenital midline abdominal wall defects at the base of the umbilical cord insertion, with herniation of gut [or occasionally other structures ] out of the fetal abdomen. • USG:- multiple bowel loops (and on occasion liver) herniate into a membrane-covered defect (i.e. not free-flowing) and are usually seen as hyperechogenic content (non-fluid filled bowel) • the umbilical cord insertion is directly into the omphalocele
  • 32.
    • Plain radiograph •In neonates, radiographs show herniated bowel loops covered by a membrane. • CT • CT, although not routinely used in neonates, permits direct visualization of herniation content +/- evidence of any malrotation. • MRI • as with CT, allows better direct visualization of the herniation through the abdominal wall • the herniated liver is often of low T2 signal and the bowel of high T2 signal
  • 33.
    THERE IS ALARGE SOFT TISSUE MASS PROJECTED OVER THE RIGHT SIDE OF THE ABDOMEN MIDLINE ABDOMINAL DEFECT WITH HERNIATION OF ABDOMINAL CONTENTS A LARGE MUSCULAR DEFECT IS SEEN IN THE ANTERIOR WALL LIVER, GB, STOMACH AND SOME OF BOWEL LOOPS ARE PROTRUDED THROUGH THE DEFECT ANTERIORLY
  • 34.
    2]GASTROSCHISIS • Extra-abdominal herniationof fetal or neonatal bowel loops (and occasionally portions of the stomach , liver , and/or gall bladder) into the amniotic cavity through a para-umbilical anterior abdominal wall defect. • USG:-The herniated content is towards the right side of the umbilical cord in most cases; color Doppler may be useful to locate the cord in relation to the herniation. This causes the fetal abdominal circumference to be smaller than expected for gestation age. The herniated bowel often appears free-floating rather than contained. The herniated bowel wall can be thickened due to edema. • There can be either accompanying oligohydramnios or polyhydramnios as ancillary sonographic sonographic features.
  • 36.
    THERE IS HERNIATIONOF SMALL BOWEL LOOPS THROUGH A RIGHT PARAUMBILICAL ABDOMINAL WALL DEFECT. AIR IS SEEN IN THE STOMACH. THERE IS NO SOLID ORGAN HERNIATION EVIDENT THERE IA AN ANTERIOR ABDOMINAL WALL DEFECT WITH PROTRUSION OF THE BOWEL LOOPS OUT THE ABDOMINAL CAVITY WITHOUT ANY COVERING
  • 37.
    3]MECKEL DIVERTICULUM • Remnantof the vitelline duct, which connects the yolk sac to the midgut through the umbilical cord. This duct is typically obliterated by the 5th to 8th week of gestation. • Fluoroscopy • Small bowel enemas have sometimes been used for the diagnosis in some centers, although a precise technique is required if the diagnosis is to be excluded with any degree of certainty 4 . • Ultrasound • Usually of limited use in the diagnosis of an uncomplicated Meckel diverticulum. Ultrasound may show a blind-ending peristaltic loop connected to the small bowel - it may have a multi-layered appearance of the wall.
  • 38.
    • CT • CTis of limited value in uncomplicated cases, as the diverticulum may resemble a normal bowel loop. CT may show a fluid- or air-filled blind-ending pouch that arises from the antimesenteric side of the distal ileum. • It is possible for the diverticulum to invert and appear as an intraluminal polypoid lesion 1
  • 39.
    FOCAL OUTPOUCHING OFMILDLY DILATED FECES-FILLED ILEUM , JUST PROXIMAL TO THE TRANSITION POINT, LIKELY DIVERTICULUM THERE IS A BLIND ENDING, AIR-FILLED , DISTENDED TUBULAR/DIVERTICULAR STRUCTURE ORIGINATING OFF THE DISTAL ILEAL BOWEL WIT THE BASE OF THE DIVERTICULUM BEAING NARROWED AT ITS ORIGIN.
  • 40.
    4]MALROTATION • In thedeveloping embryo growth of the bowel requires herniation into the omphalomesenteric sac. In the tenth week of gestation the bowel returns to the abdominal cavity. • This return is accompanied by a counterclockwise rotation of the midgut to achieve its final position with the ligament of Treitz in the left upper quadrant and the caecum in the right lower quadrant, suspended from a long mesentery. • Malrotation arises when the rotation is arrested or even reversed. As a result the bowel has an abnormal position, the mesentery is short and peritoneal bands, called Ladd's bands, may cross from the caecum to the liver or to the anterior abdominal wall.
  • 41.
    • Left Normal situationwith the duodenum retroperitoneal. Treitz ligament is on the left side of the spine. The small intestine is predominantly on the left. The cecum is in the right lower quadrant There is a long mesentery. • Middle Displacement of Treitz inferiorly and rightward. The small intestine is found predominantly on the right. Fibrous bands course over the vertical portion of the duodenum causing obstruction. • Right Volvulus due to short mesentery. Ischemic bowel.
  • 42.
    • The malrotationwill become symptomatic only when a volvulus occurs due to the short mesentery or when the Ladd's band obstruct the duodenum • Both presentations are most common in the neonatal period. • However sometimes it can also present later in life, for example when the volvulus is intermittent or when the Ladd's bands create relatively little obstruction. • Acute volvulus is a life-threatening presentation and requires prompt surgical intervention.
  • 43.
    • The upperGI-study shows a malrotation complicated by a volvulus. • This results in the typical corkscrew or reversed 3 sign. • An overfilled stomach could hide the corkscrew on the AP projection so the stomach should first be aspirated by use of a nasogastric tube and the volume of injected contrast should be small.
  • 44.
    • Sometimes amalrotation can be suspected when on ultrasound the superior mesenteric artery is seen to lie to the right of the superior mesenteric vein. • This sign however is neither specific nor sensitive and should not be used when asked to investigate for suspected malrotation without a volvulus. • An abnormal location of ligament of Treitz on an upper GI series is the gold standard for malrotation.
  • 45.
    • In caseof a volvulus the child is acutely sick and ultrasound is often the modality of choice. • This will show a whirlpool sign of the vessels which confirms the presence of a volvulus. • The corkscrew sign of the bowel on the upper GI is equivalent. Once a volvulus is diagnosed on ultrasound, the child should go straight to the operating room and no more time should be lost on further imaging.
  • 46.
    USG showing whirlpoolsign of vessels which confirms the presence of volvulus
  • 47.
    14 DAYS MALEBABY OF BHAVANI
  • 51.
    5] DUODENAL ATRESIA/STENOSIS •Duodenal atresia results from a congenital malformation of the duodenum and requires prompt correction in the neonatal period. It is considered to be one of the commonest causes of fetal bowel obstruction. • Plain radiograph • Abdominal radiographs may classically show a double bubble sign with gas filled distended stomach and duodenum with an absence of distal gas. A similar appearance (either filled with fluid or gas) can be seen in other modalities.
  • 52.
    • Barium study •Barium contrast can be administered sometimes via an orogastric or nasogastric tube under fluoroscopy to evaluate the upper gastrointestinal tract. Only a controlled amount of barium is placed to confirm obstruction. It is then removed by nasogastric tube to prevent reflux and potential aspiration.
  • 53.
    • Ultrasound • Mayalso show a dilated stomach and duodenum giving a double bubble type appearance. This, however, may not be sonographically detectable until the mid to late second trimester. May also show evidence of polyhydramnios as an ancillary sonographic feature. • If a double-bubble sign is seen on antenatal ultrasound, then it is important to demonstrate a connection between the two fluid- filled structures because foregut duplication cyst, as well as other abdominal cysts, may simulate the appearance of a double-bubble sign. • Likewise, a "double bubble" may be seen in cases of Ladd's bands, annular pancreas or volvulus, in which there is no duodenal atresia.
  • 54.
    Gaseous distension ofstomach and proximal duodenum with absence of bowel gas distally giving the classical appearance of double bubble sign, compatible with duodenal atresia. Antenatal ultrasound showing increased liquor amnii (polyhydramnios) with two communicating cystic structures in upper abdomen of the fetus suggestive of double bubble sign and representing over distended fetal stomach and proximal duodenum.
  • 55.