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Imaging in neonatal GIT
S. THIYAGARAJAN
Clinical manifestation
The most common clinical findings
ā€¢ Inability to pass RT
ā€¢ Vomiting
ā€¢ Abdominal distension
ā€¢ Failure to pass meconium/imperforate
anus
ā€¢ AN detected
GI Causes of Vomiting
Bilious
ā€¢ Infant/Child
ā€¢ Intussusception
ā€¢ Malrotation w/ volvulus
ā€¢ Incarcerated hernia
ā€¢ Neonate
ā€¢ Congenital Atresia
ā€¢ Meconium Ileus
ā€¢ NEC
ā€¢ Hirschsprungā€™s
Nonbilious
ā€¢ Infant/Child
ā€¢ Gastroenteritis
ā€¢ GERD
ā€¢ Hepatobiliary
ā€¢ Pancreatitis
ā€¢ PUD
ā€¢ Gastroparesis
ā€¢ Appendicitis
ā€¢ Neonate
ā€¢ Pyloric Stenosis
Esophageal Atresia &
Tracheoesophageal Fistula
ā€¢ Developmental disorder
ā€¢ Fault in formation and separation of
the primitive foregut into the trachea
and esophagus
TYPE A
TYPE B
TYPE C
TYPE D
TYPE E
Radiography
ā€¢ Radiographic evaluation should always
include the abdomen to assess the
presence of air in the GI tract
ā€¢ Blind pouch of the proximal esophagus
that is distended with air
ā€¢ Type A and B - Complete absence of gas in
the stomach and intestinal tract
ā€¢ Type C and D - GIT commonly appears
distended with air.
ā€¢ The type of esophageal atresia is
confirmed by advancing a radiopaque
feeding tube through the nose to the level
of the atresia
ā€¢ The tube will curl when it approaches the
blind end
ā€¢ Atelectasis and pneumonia involving the
upper right lobe
ā€¢ Type E (H-shaped TE fistula without
atresia) - Demonstration of the fistula,
which typically courses forward and
upward from the esophagus
Oesophageal
atresia
Esophageal Atresia and
Tracheoesophageal Fistula
ā€¢ 25% associated with other GI
malformations
ā€¢ Imperforate anus
ā€¢ Pyloric stenosis
ā€¢ Duodenal atresia
ā€¢ Annular pancreas
ā€¢ Less frequently, cardiac, genitourinary, and
vertebral alterations
Esophageal Atresia and
Tracheoesophageal Fistula
ā€¢ The VACTERL complex
ā€¢ Vertebral
ā€¢ Anal
ā€¢ Cardiac
ā€¢ Tracheal
ā€¢ Esophageal
ā€¢ Renal
ā€¢ Limb anomalies
ā€¢ The best known grouping of anomalies
associated with tracheoesophageal lesions
VACTERL
Oesophageal
atresia with
absent radius -
thumb
Gastrointestinal duplications
ā€¢ Three defining characteristics
ā€¢ Have well developed coat of smooth
muscle
ā€¢ Epithelial lining represents some part of
the alimentary tract
ā€¢ Attached to some part of the alimentary
tract
ā€¢ Part of the spectrum of mesenteric and
omental cyst
ā€¢ Can occur anywhere along the
alimentary tract
ā€¢ Duplication cysts are most often
associated with the esophagus and
jejunum/ileum
Esophageal duplications
ā€¢ More often seen on the right side
ā€¢ More common in the lower half of the
chest
ā€¢ Contain gastric mucosa in 30%
ā€¢ Often have associated vertebral
anomalies (neurenteric cyst)
Esophageal
duplications
HYPERTROPHIC PYLORIC
STENOSIS
ā€¢ Idiopathic thickening of pyloric muscle
in infancy which creates progressive
gastric outlet obstruction
ā€¢ Typically seen in 2-8 week old infants
with worsening projectile vomiting
ā€¢ Incidence of - 2 per 1,000 live births
Radiographic Findings
ā€¢ Overdistended stomach and minimal
bowel gas distally
ā€¢ Stomach may be collapsed if infant has
recently vomited
UGI findings
ā€¢ Pyloric wall thickness >10 mm
ā€¢ Elongation and narrowing of pyloric canal
(2-4 cm in length)
ā€¢ "Double / triple track sign"
ā€¢ Crowding of mucosal folds in pyloric channel
ā€¢ "String sign"
ā€¢ Passing of small barium streak through pyloric
channel
ā€¢ Twining recess = "diamond sign"
ā€¢ Transient triangular tentlike cleft / niche in
midportion of pyloric canal with apex
pointing inferiorly secondary to mucosal
bulging between two separated hypertrophied
muscle bundles on the greater curvature side
within pyloric channel
ā€¢ "Pyloric teat"
ā€¢ Outpouching along lesser curvature due to
disruption of antral peristalsis
ā€¢ "Antral beaking"
ā€¢ Mass impression upon antrum with streak of
barium pointing toward pyloric channel
ā€¢ Kirklin sign = "mushroom sign"
ā€¢ Indentation of base of bulb (in 50%)
ā€¢ Gastric distension with fluid
ā€¢ Active gastric hyperperistalsis
ā€¢ "Caterpillar sign"
RADIOLOGICAL SIGNS
beak
caterpillar
mush diamond
teat
track
shoulder
US findings
ā€¢ "Target sign"
ā€¢ Hypoechoic ring of hypertrophied pyloric
muscle around echogenic mucosa centrally
on cross-section
ā€¢ "Cervix sign"
ā€¢ Indentation of muscle mass on fluid-filled
antrum on longitudinal section
ā€¢ "Antral nipple sign"
ā€¢ Redundant pyloric channel mucosa
protruding into gastric antrum
US findings
ā€¢ Thickened pylorus
Commonly accepted threshold values
ā€¢ Single wall thickness of pylorus > 3 mm
ā€¢ Pyloric channel length > 16 mm
ā€¢ Pyloric diameter > 7 mm
ā€¢ Exaggerated peristaltic waves
ā€¢ Delayed gastric emptying of fluid into
duodenum
ā€¢ Complications: Hypochloremic metabolic
alkalosis
US findings
ā€¢ Pyloric volume >1.4 cm3
[maximum pyloric diameter]2 x pyloric length
4
ā€¢ Most criteria independent of contracted or
relaxed state
ā€¢ [Pyloric length (mm) + 3.64] x muscle thickness (mm) > 25
Pyloric stenosis
Target sign
Antral nipple sign
Redundant pyloric cannal mucosa
protruding into gastric antrum
Cervix sign
Indentation of the pylorus
into the fluid-filled antrum
GASTRIC VOLVULUS
ā€¢ Rotation all or part of stomach > 180
degrees, Ā± closed-loop obstruction,
possible strangulation
ā€¢ It is the rotation and not the obstruction
which defines the presence of volvulus
ā€¢ Organoaxial volvulus: Rotation around
longitudinal axis (most common)
ā€¢ Around line extending from cardia to pylorus
ā€¢ Stomach twists anteriorly or posteriorly
ā€¢ Antrum moves inferior to superior
ā€¢ Mesenteroaxial volvulus: Rotation about
mesenteric axis
ā€¢ Axis running across stomach right angles to
lesser & greater curves
ā€¢ Rotation right to left or left to right about
gastrohepatic omentum
ā€¢ Mixed volvulus
ā€¢ Combination of
OAV & MAV
Radiography
ā€¢ Abdominal plain films; patient upright
ā€¢ Double air-fluid level
ā€¢ Large, distended stomach; spheric viscus
displaced upward to left
ā€¢ Elevation of diaphragm
ā€¢ Small bowel collapsed; paucity distal gas
ā€¢ Intramural emphysema gastric wall
ā€¢ Chest X-ray
ā€¢ Intrathoracic up-side down stomach
ā€¢ Retrocardiac fluid level
ā€¢ 2 air-fluid interfaces different heights
ā€¢ Simultaneous fluid levels above & below
diaphragm
Fluoroscopic Findings
ā€¢ Massively distended stomach left upper
quadrant, may extending into chest
ā€¢ Inversion of stomach
ā€¢ Greater curvature above lesser
ā€¢ Cardia & pylorus at same level
ā€¢ Downward pointing pylorus & duodenum
ā€¢ May see "beaking" at point of twist
ā€¢ OAV: 2 points of twist; luminal obstruction
ā€¢ Contrast in stomach may not pass beyond
pylorus
ā€¢ MAV: Antrum & pylorus lie above gastric
fundus
Organoaxial
volvulus
CT Findings
ā€¢ Not generally performed for GV
ā€¢ CT appearance may be variable
ā€¢ Depends on extent of gastric herniation,
points of torsion, position of stomach
ā€¢ May be linear septum within gastric lumen
(area of torsion)
ā€¢ Large hiatal hernia accompanied by
partial GV
ā€¢ "Pseudothrombosis" of inferior vena cava
on CT
Mesenteroaxial
gastric volvulus
DUODENUM
Duodenal Obstruction
ā€¢ Complete duodenal obstruction is seen
much more frequently than congenital
gastric obstruction.
ā€¢ Vomiting is usually delayed until after
the first feeding but increases
progressively thereafter
Radiographic Appearance of
Duodenal Obstruction
Complete obstruction
ļƒ¼ Gasless abdomen
ļƒ¼ Gas in stomach and prox. duodenum
ļƒ¼ Gas distally if bifid common bile duct
Partial obstruction
ļƒ¼ Gastric distention
ļƒ¼ Distended small bowel
ļƒ¼ ā€œDouble bubbleā€
ļƒ¼ Scattered gas-filled bowel loops distally
ļƒ¼ Normal if vomiting decompressed stomach and
duodenum
DDX Duodenal Obstruction
ā€¢ Intrinsic (Often complete obstruction)
-Duodenal atresia
-Duodenal stenosis
-Duodenal web, diaphragm, or ā€œwind sockā€
ā€¢ Extrinsic (Often partial obstruction)
-Malrotation with midgut volvulus
-Malrotation with Laddā€™s bands
-Annular pancreas
-Preduodenal portal vein
-Hematoma
Duodenal atresia
ā€¢ Most important cause of complete
duodenal obstruction.
ā€¢ Failure of recanalization of the
duodenum between approximately the
9th and 11th weeks of gestation
Jejunal atresia
ā€¢ Normal or near normal size colon
ā€¢ Seen in jejunal and proximal ileal atresias
ā€¢ Colon receives succus entericus from
remaining small bowel
Jejunoileal
atresia
JEJUNOILEAL ATRESIA
Ileal atresia - Contrast enema
ā€¢ Microcolon (small unused colon)
ā€¢ The earlier in gestation the obstruction
occurs
Ileal atresia
Small Bowel
Atresia Ba
enema
Rotation of Gut
Abnormal Gut Rotation
ā€¢ Nonrotation
ā€¢ When both limbs return to abdomen without further
rotation
ā€¢ Small bowel on right and colon on left
ā€¢ Wide mesentery ā€“ less risk of volvulus
ā€¢ Gastroschisis; Omphalocele; Diaphragmatic Hernia
ā€¢ Malrotation
ā€¢ Duodenojejunal limb remains in nonrotation in the
right midabdomen
ā€¢ Cecocolic limb in partial rotation in the midupper
abdomen fixed to abdominal wall by Ladds bands
Malrotation - Radiography
ā€¢ X ray abdomen : less informative
ā€¢ Abnormal configuration of gas in right
hypochondrium, the duodenal triangle suggests
diagnosis
ā€¢ Volvulus :
ā€¢ Corkscrew sign
ā€¢ Tapering of beaking of the bowel in complete obstruction
ā€¢ Malrotated bowel configuration
ā€¢ Distal obstruction
ā€¢ Closed loop syndrome features - thick walled
edematous loops with pneumatosis
ā€¢ Gas less abdomen due to prolonged vomiting
ā€¢ Upper GI series - Modality of choice
ā€¢ Clearly abnormal position of
duodenum (81%)
ļƒ˜Duodenum and Jejunum to right of spine
ļƒ˜Corkscrew duodenum and jejunum
ļƒ˜DJJ low and in midline
ā€¢ Unusual abnormal position of
duedenum (16%)
ļƒ˜ DJJ over right pedicle
ļƒ˜ DJJ left of spine but low
ļƒ˜ Duodenal redundency to right of spine
ļƒ˜ Z shaped configuration of duodenum &
Jejunum
USG - Midgut volvulus
ā€¢ Clockwise whirlpool sign
ā€¢ Abnormal superior mesenteric vessels
ā€¢ Inverted SMA/SMV relationship
ā€¢ Solitary hyperdynamic pulsating SMA
ā€¢ Truncated SMA
ā€¢ Inapparent SMV
ā€¢ Abnormal bowel
ā€¢ Dilated duodenum proximal to obstruction
ā€¢ Thickened wall of small bowel distal to
obstruction
ā€¢ Dilated fluid filled loops of small bowel
ā€¢ Ascites
CT
ā€¢ SMV to the left of SMA in 80%
ā€¢ Aplastic or hypoplastic uncinate process
of pancreas
ā€¢ Chylous mesentric cyst (from interference
of lymphatic drainage)
ā€¢ Midgut volvulus
ā€¢ Whirlpool sign of twisted mesentary
ā€¢ Bowel obstruction
ā€¢ Free fluid / free gas in advanced cases
Whirlpool sign
Whirlpool sign
Angiography
ā€¢ Barber pole sign ā€“ spiralling of SMA
ā€¢ Tapering or abrupt termination of
mesentric vessels
ā€¢ Mesentric vasoconstriction
ā€¢ Prolonged contrast transit time
ā€¢ Absent venous opacification
ā€¢ Dilated tortures superior mesentric
vein.
INTUSSUSCEPTION
ā€¢ Invagination of more proximal bowel
(the intussusceptum) into lumen of
more distal bowel (the intussuscipiens)
in a telescope-like manner
ā€¢ Most common site:
ā€¢ Terminal ileum/ileocecal valve
ā€¢ 90% ileocolic
Radiography
ā€¢ Soft tissue mass surrounded by a crescent
of gas
ā€¢ Evidence of distal small bowel obstruction
ā€¢ Absence of or decreased gas in the colon
ā€¢ Pneumoperitoneum
ā€¢ May be normal
ā€¢ Left-side-down decubitus/prone views can be
helpful in showing lack of air-filled cecum
Intussusception
ā€¢ Meniscus sign
Produced by the rounded apex of the
intussusceptum protruding into the column
of contrast
ā€¢ Coiled spring appearance
Edematous mucosal folds of the returning
limb of the intussusceptum are outlined by
contrast material in the lumen of the colon
Intussusception
Target sign (Doughnut sign)
USG
Pseudokidney
sign / Hay fork
sign
USG
Mesenteric vessels dragged between entering and
returning wall of intussusceptum
Intussusception
DIFFERENTIAL DIAGNOSIS
ā€¢ Normal position of sigmoid colon
ā€¢ Appendicitis
ā€¢ Gastroenteritis
ā€¢ Ovarian pathology
ā€¢ Meckel diverticulum
MECKEL DIVERTICULUM
ā€¢ Remnant of the omphalomesenteric duct
ā€¢ Bleeding (when contain ectopic gastric mucosa)
ā€¢ Intussusception
ā€¢ Bowel obstruction
ā€¢ Perforation
ā€¢ Rule of 2's :
ā€¢ 2% Incidence of general population
ā€¢ 2 feet of ileocecal valve
ā€¢ Before age 2 years
Radiography
ā€¢ Right lower quadrant mass
ā€¢ Displacement of bowel loops,
ā€¢ Obstruction
ā€¢ Enteroliths
ā€¢ May be normal
Fluoroscopic Findings
ā€¢ Barium studies show indirect evidence
of mass and inflammatory changes in
adjacent bowel
Ultrasonographic Findings
ā€¢ Heterogeneous echotexture mass in
RLQ, may mimic appendicitis
ā€¢ Thick walled tubular structure or
hyperemic bowel loops in RLQ
ā€¢ Inflamed Meckel diverticulum may
present as a cyst
CT Findings
ā€¢ Findings very similar to appendicitis
ā€¢ Thick walled blind ending structure near
cecum with surrounding inflammation
ā€¢ If perforated may see abscess and free air
ā€¢ CT is more accurate in diagnosing Meckel
diverticulum than arteriography when
presenting symptom is gastrointestinal
bleeding in pediatric patients
Nuclear Medicine Findings
Tc-99m pertechnetate scan
ā€¢ The most specific test for Meckel diverticulum is the
Tc-99m pertechnetate scan: Accuracy -90%
ā€¢ Pertechnetate accumulates in mucous cells when they
are in an acidic environment, in this case in ectopic
gastric mucosa
ā€¢ The diverticulum typically does not communicate
with the bowel lumen, so the radiotracer does not
appear to move downstream in bowel unless there is
active bleeding
MECONIUM PLUG
SYNDROME
ā€¢ Small left colon syndrome.
ā€¢ Transient functional obstruction of the
newborn colon
ā€¢ Common cause of distal neonatal bowel
obstruction
Radiography
ā€¢ Multiple dilated loops of bowel
ā€¢ Cannot differentiate dilated large from
small bowel loops in neonates
ā€¢ Findings nonspecific, cannot
differentiate from other causes of distal
bowel
Contrast enema
ā€¢ R/S ratio usually> 1
ā€¢ Descending and sigmoid colon small in
caliber
ā€¢ Abrupt zone of caliber transition in region of
splenic flexure
ā€¢ Filling defects within colon
ā€¢ Ascending and transverse colon increased in
caliber
ā€¢ Difficult to differentiate from long segment
Hirschsprung disease
ā€¢ Enema often therapeutic; passage of
meconium plugs during or just after enema
Small left colon syndrome
ā€¢ Functional immaturity of colon
ā€¢ Narrow caliber of the left colon.
ā€¢ Abrupt transition at the splenic flexure.
ā€¢ Multiple filling defects in the left colon
are due to meconium plugs
ā€¢ These infants present at 1-2 days of age
with failure to pass meconium.
MECONIUM ILEUS
ā€¢ Neonatal obstruction of the distal ileum
due to abnormally thick, tenacious
meconium
ā€¢ Meconium becomes inspissated and
obstructs the distal ileum and is usually
a manifestation of cystic fibrosis
ā€¢ Presenting illness in approximately 15%
of CF patients
Radiography
ā€¢ Difficult to distinguish neonatal large vs. small
bowel
ā€¢ Uncomplicated Type
ā€¢ Multiple dilated bowel loops
ā€¢ Bubbly lucencies right lower quadrant
ā€¢ Few air-fluid levels (sticky meconium)
ā€¢ Complicated Type
ā€¢ Soft tissue mass or gas less abdomen
ā€¢ Ā± Intrauterine perforation and peritonitis
ā€¢ Curvilinear calcifications on peritoneal surface or lining
pseudocyst
ā€œBubbly"
appearance
of the
distended
intestinal
loops
Contrast enema
ā€¢ Smallest of microcolons
ā€¢ Reflux contrast into terminal ileum
ā€¢ Meconium pellets in terminal ileum; not
much in colon
ā€¢ Can be therapeutic in uncomplicated
type
Meconium ileus
MECONIUM PERITONITIS
ā€¢ Chemical peritonitis from in utero
bowel perforation and peritoneal
leakage of sterile meconium
ā€¢ At least four types are recognised:
ā€¢Fibro-adhesive
ā€¢Cystic
ā€¢Generalised
ā€¢Healed
Meconium
peritonitis
Soft tissue mass,
punctate or
curvilinear
calcifications,
ascites, dilated
bowel loops
Meconium peritonitis
AN - USG
ā€¢ Highly echogenic linear or clumped foci
(calcifcation )
ā€¢ Snowstorm appearance
ā€¢ Abdominal circumference may be increased
ā€¢ Associated anomalies such as dilated fetal bowel
and/or meconium pseudocysts
ā€¢ Meconium pseudocyst: Heterogeneous mass
with calcified wall
ā€¢ Fetal ascites and/or polyhydramnios
NECROTIZING
ENTEROCOLITIS
ā€¢ Idiopathic enterocolitis
ā€¢ VLBW premature infants
ā€¢ Combination of infection and ischemia
characterized by coagulative and
hemorrhagic necrosis
ā€¢ Inflammation of portions of the small
and large intestine
Location
ā€¢ Most common right colon and terminal
ileum
ā€¢ Can occur anywhere in gastrointestinal
tract
Radiography
ā€¢ Findings range from normal to suggestive
to diagnostic
ā€¢ Normal
ā€¢ Suggestive findings
ā€¢ Asymmetric bowel dilation
ā€¢ Featureless "unfolded" bowel loops
ā€¢ Separation of bowel loops
ā€¢ Fixed configuration of bowel loops over serial
films
Necrotising
enterocolitis
Definitive finding:
Pneumatosis
Bubble-like
(submucosal)
or curvilinear
(serosal)
lucencies
Pneumatosis
intestinalis
(intramural gas)
Portal venous gas
Definitive finding: Portal venous gas
Branching lucencies over the liver
The football sign / air dome sign
ā€¢ Right upper quadrant
gas
ā€¢ Riglerā€™s (double wall)
sign
ā€¢ Ligament visualization
ā€¢ Inverted V sign
ā€¢ Triangular air
ā€¢ The cupola sign
ā€¢ Football or air dome
ā€¢ Scrotal air
Definitive finding: Free intraperitoneal air
Bell classification
ā€¢ Stage I: Early or suspected NEC
ā€¢ Nonspecific
ā€¢ Scalloping/separation/unfolding bowel loops
ā€¢ Asymmetric bowel distention
ā€¢ Stage II: Definite NEC
ā€¢ Pneumatosis intestinalis: Mucosal, serosal; not always
correlating with clinical symptoms/signs
ā€¢ Stage III:
ā€¢ Advanced disease (perforation or impending
perforation)
ā€¢ PVG, free intraperitoneal air, persistent loop sign,
ascites
Fluoroscopic Findings
ā€¢ Enema contraindicated in presumed
acute NEC
ā€¢ Mucosa permeable to water-soluble
contrast and excreted into kidneys
ā€¢ Stricture:
ā€¢ Single or multiple
ā€¢ Small bowel or colon
ā€¢ Chronic complication of NEC
Ultrasonographic Findings
ā€¢ Thickened bowel wall loops
ā€¢ Increased (inflamed) or decreased
(infarcted) vascularity
ā€¢ Ascites
Differential diagnosis
ā€¢ In the correct clinical scenario the
presence of gas within bowel wall has
little differential.
ā€¢Pneumatosis coli
ā€¢Neonatal appendicitis
ā€¢Meconium ileus
ā€¢Hirschsprung disease
ā€¢Infectious enterocolitis
HIRSCHSPRUNG DISEASE
ā€¢ Functional obstruction of the bowel due to
lack of intrinsic enteric ganglion cells
ā€¢ Morphology
ā€¢ Denervated colon is small, narrow, spasmodic
ā€¢ Innervated more proximal bowel is dilated
ā€¢ Affected portion always includes the anus and
variable length of Rectum
ā€¢ Continuous disease
ā€¢ No proximal without distal involvement
ā€¢ Short segment disease : ~ 75% *
ā€¢ Rectal and distal sigmoid colonic involvement only
ā€¢ Long segment : ~ 15%
ā€¢ Typically extends to splenic flexure / transverse colon
ā€¢ Total colonic aganglionosis : 2 - 13%
ā€¢ Zuezler-Wilson syndrome
ā€¢ Occasional extension of aganglionosis into small
bowel
ā€¢ Ultrashort segment disease
ā€¢ 3 ā€“ 4 cm of internal anal sphincter only
ā€¢ Controversial entity
Associations
ā€¢ Isolated abnormality in 70% of cases
ā€¢ Down syndrome : in ~ 10%
ā€¢ Neurocristopathy syndromes
ā€¢ Waardenburg-Shah syndrome
ā€¢ Haddad syndrome
ā€¢ MEN IIa
ā€¢ other non-neurocristopathy syndromes
ā€¢ Aarskog syndrome
ā€¢ Bardet-Biedl syndrome
ā€¢ Fryns syndrome
ā€¢ Pallister-Hall syndrome
ā€¢ Smith-Lemli-Opitz syndrome
Radiography
ā€¢ Multiple
loops of
dilated
bowel
ā€¢ Paucity of
gas in the
rectum
Contrast enema
ā€¢ Rectum smaller than sigmoid (R/S ratio < 1)
ā€¢ Transition zone from abnormally small distal to
dilated proximal colon
ā€¢ Fasciculations or sawtooth appearance of mucosa of
involved colon: Spasm
ā€¢ Thickened, ulcerated colon in patients with
associated colitis
ā€¢ Microcolon: Total colonic disease
Differential diagnosis
ā€¢ Functional megarectum
ā€¢ Necrotising enterocolitis
ā€¢ Microcolon : appears similar to long
segment / whole colon Hirschsprung
disease
Megacystis-microcolon-intestinal
hypoperistalsis syndrome
ā€¢ The duodenum and proximal jejunum
are mildly dilated.
ā€¢ Small bowel is dilated and shortened,
and the colon is a microcolon
ā€¢ Abundance of ganglion cells in the
entire gastrointestinal tract.
ā€¢ Megacystis and megaureters
ANORECTAL
MALFORMATION
ā€¢ Abnormal separation of genitourinary
system from hindgut
ā€¢ Spectrum; true imperforate anus (thin
membrane) to atresia distal rectum
ā€¢ Classification controversial
ā€¢ Anatomic: Relation of rectal pouch to
pubococcygeal line
ā€¢ Surgical: Prognostic and therapeutic, "Penaā€œ
classification
ā€¢ Low
ā€¢ Usually visible perineal orifice; stenotic or
membrane
ā€¢ No GU tract communication
ā€¢ Intermediate
ā€¢ Usually features of high lesion
ā€¢ High
ā€¢ Usually rectourinary fistula in males
ā€¢ Usually rectovaginal or vestibular in females
ā€¢ Possible vaginal, uterine, or bladder anomalies
PUBOCOCCYGEAL LINE:
ā€¢ Line is drawn between upper and
middle third of pubis to lower border
of S5
ā€¢ Bowel ends just above this line are
termed high malformation and below
one is termed low malformation.
ISCHIAL LINE
ā€¢ Line drawn below parallel to the
pubococcygeal line at the level of the ossified
ischial bone
ā€¢ Corresponds to the most proximal level of
bulbous urethra
ā€¢ Anomalies between this two lines are termed
intermediate
ā€¢ If fistulas occur, they open in the bulbous
urethra in male or in to vestibule or lower part
of vagina in the female.
PIT LINE
ā€¢ This line is parellal to the ischial line but
one to two centimetre caudal to it.
ā€¢ This marks the posteroinferior part of
the bulbocavernous muscle.
ā€¢ If bowel gas ended below this area
Called imperforate anal membrane or
low ARM
Radiography
ā€¢ Distal bowel obstruction, intraluminal
calcification
ā€¢ Ā± Gas in bladder in males, vagina in females
ā€¢ Air in rectal pouch on prone cross table
lateral view: Inaccurate for level
ā€¢ Bony landmark PCL
ā€¢ "M" line: Horizontal to pelvis divides lower 1/3,
upper 2/3 ischium
ā€¢ Low lesions appear high: Meconium-packed
pouch
ā€¢ High lesions appear low: Straining, crying,
excessive distention pouch
ARM
Voiding Cystourethrogram
ā€¢ Catheter into cloaca (single perineal orifice)
ā€¢ Enters bladder, vagina, or colon
ā€¢ Bladder findings
ā€¢ Normal; vesicoureteral reflux (VUR); wall-
thickening; neurogenic bladder; fistula to rectum
ā€¢ Urethral findings
ā€¢ Opens to cloaca, fistula from rectum to posterior>
bulbous> penile urethra
ā€¢ Vaginal findings
ā€¢ Normal; rectovaginal fistula; congenital anomalies
(septate, duplicated, etc.)
High pressure
distalcolostography
ā€¢ Several months after colostomy prior to
repair
ā€¢ Key view is lateral
ā€¢ Document connection to urethra,
bladder, or vagina
Ultrasound
ā€¢ Hypoechoic rectal pouch-perineal
distance
ā€¢ < 10 mm: Low lesion;
ā€¢ > 10-15 mm - high or intermediate
ā€¢ Reliability similar to radiography with
similar inaccuracies
MR Findings
ā€¢ Pelvic musculature, neorectum, and anal
sphincter position/integrity
ā€¢ Normal to absent levator muscle
ā€¢ Normal to absent anal sphincter complex
ā€¢ Muscle complex malpositioned or atrophic
ā€¢ Spine
ā€¢ Tethered cord, spinal dysraphism, sacral
agenesis
Urinary tract anomalies associated with ARM
ā€¢ Renal agenesis
ā€¢ Renal ectopia
ā€¢ Megaureter
ā€¢ HN (PUJ obstruction)
ā€¢ VUR
ā€¢ PUV
ā€¢ Epispadias/Hypo
ā€¢ Prune belly syn
ā€¢ VATER anomaly
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
To summarizeā€¦
Announcement!!!
GUEST LECTURE
On
By
Consultant Radiologist,
Apollo hospitals, Madurai.
Date: 12.11.2011,Saturday

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IMAGING IN NEONATAL GIT

  • 1. Imaging in neonatal GIT S. THIYAGARAJAN
  • 2. Clinical manifestation The most common clinical findings ā€¢ Inability to pass RT ā€¢ Vomiting ā€¢ Abdominal distension ā€¢ Failure to pass meconium/imperforate anus ā€¢ AN detected
  • 3. GI Causes of Vomiting Bilious ā€¢ Infant/Child ā€¢ Intussusception ā€¢ Malrotation w/ volvulus ā€¢ Incarcerated hernia ā€¢ Neonate ā€¢ Congenital Atresia ā€¢ Meconium Ileus ā€¢ NEC ā€¢ Hirschsprungā€™s Nonbilious ā€¢ Infant/Child ā€¢ Gastroenteritis ā€¢ GERD ā€¢ Hepatobiliary ā€¢ Pancreatitis ā€¢ PUD ā€¢ Gastroparesis ā€¢ Appendicitis ā€¢ Neonate ā€¢ Pyloric Stenosis
  • 4. Esophageal Atresia & Tracheoesophageal Fistula ā€¢ Developmental disorder ā€¢ Fault in formation and separation of the primitive foregut into the trachea and esophagus
  • 10. Radiography ā€¢ Radiographic evaluation should always include the abdomen to assess the presence of air in the GI tract ā€¢ Blind pouch of the proximal esophagus that is distended with air ā€¢ Type A and B - Complete absence of gas in the stomach and intestinal tract ā€¢ Type C and D - GIT commonly appears distended with air.
  • 11. ā€¢ The type of esophageal atresia is confirmed by advancing a radiopaque feeding tube through the nose to the level of the atresia ā€¢ The tube will curl when it approaches the blind end ā€¢ Atelectasis and pneumonia involving the upper right lobe ā€¢ Type E (H-shaped TE fistula without atresia) - Demonstration of the fistula, which typically courses forward and upward from the esophagus
  • 13. Esophageal Atresia and Tracheoesophageal Fistula ā€¢ 25% associated with other GI malformations ā€¢ Imperforate anus ā€¢ Pyloric stenosis ā€¢ Duodenal atresia ā€¢ Annular pancreas ā€¢ Less frequently, cardiac, genitourinary, and vertebral alterations
  • 14. Esophageal Atresia and Tracheoesophageal Fistula ā€¢ The VACTERL complex ā€¢ Vertebral ā€¢ Anal ā€¢ Cardiac ā€¢ Tracheal ā€¢ Esophageal ā€¢ Renal ā€¢ Limb anomalies ā€¢ The best known grouping of anomalies associated with tracheoesophageal lesions
  • 17. Gastrointestinal duplications ā€¢ Three defining characteristics ā€¢ Have well developed coat of smooth muscle ā€¢ Epithelial lining represents some part of the alimentary tract ā€¢ Attached to some part of the alimentary tract ā€¢ Part of the spectrum of mesenteric and omental cyst
  • 18. ā€¢ Can occur anywhere along the alimentary tract ā€¢ Duplication cysts are most often associated with the esophagus and jejunum/ileum
  • 19. Esophageal duplications ā€¢ More often seen on the right side ā€¢ More common in the lower half of the chest ā€¢ Contain gastric mucosa in 30% ā€¢ Often have associated vertebral anomalies (neurenteric cyst)
  • 21.
  • 22. HYPERTROPHIC PYLORIC STENOSIS ā€¢ Idiopathic thickening of pyloric muscle in infancy which creates progressive gastric outlet obstruction ā€¢ Typically seen in 2-8 week old infants with worsening projectile vomiting ā€¢ Incidence of - 2 per 1,000 live births
  • 23. Radiographic Findings ā€¢ Overdistended stomach and minimal bowel gas distally ā€¢ Stomach may be collapsed if infant has recently vomited
  • 24.
  • 25. UGI findings ā€¢ Pyloric wall thickness >10 mm ā€¢ Elongation and narrowing of pyloric canal (2-4 cm in length) ā€¢ "Double / triple track sign" ā€¢ Crowding of mucosal folds in pyloric channel ā€¢ "String sign" ā€¢ Passing of small barium streak through pyloric channel
  • 26. ā€¢ Twining recess = "diamond sign" ā€¢ Transient triangular tentlike cleft / niche in midportion of pyloric canal with apex pointing inferiorly secondary to mucosal bulging between two separated hypertrophied muscle bundles on the greater curvature side within pyloric channel ā€¢ "Pyloric teat" ā€¢ Outpouching along lesser curvature due to disruption of antral peristalsis ā€¢ "Antral beaking" ā€¢ Mass impression upon antrum with streak of barium pointing toward pyloric channel
  • 27. ā€¢ Kirklin sign = "mushroom sign" ā€¢ Indentation of base of bulb (in 50%) ā€¢ Gastric distension with fluid ā€¢ Active gastric hyperperistalsis ā€¢ "Caterpillar sign"
  • 29.
  • 30. US findings ā€¢ "Target sign" ā€¢ Hypoechoic ring of hypertrophied pyloric muscle around echogenic mucosa centrally on cross-section ā€¢ "Cervix sign" ā€¢ Indentation of muscle mass on fluid-filled antrum on longitudinal section ā€¢ "Antral nipple sign" ā€¢ Redundant pyloric channel mucosa protruding into gastric antrum
  • 31. US findings ā€¢ Thickened pylorus Commonly accepted threshold values ā€¢ Single wall thickness of pylorus > 3 mm ā€¢ Pyloric channel length > 16 mm ā€¢ Pyloric diameter > 7 mm ā€¢ Exaggerated peristaltic waves ā€¢ Delayed gastric emptying of fluid into duodenum ā€¢ Complications: Hypochloremic metabolic alkalosis
  • 32. US findings ā€¢ Pyloric volume >1.4 cm3 [maximum pyloric diameter]2 x pyloric length 4 ā€¢ Most criteria independent of contracted or relaxed state ā€¢ [Pyloric length (mm) + 3.64] x muscle thickness (mm) > 25
  • 34.
  • 36. Antral nipple sign Redundant pyloric cannal mucosa protruding into gastric antrum
  • 37. Cervix sign Indentation of the pylorus into the fluid-filled antrum
  • 38. GASTRIC VOLVULUS ā€¢ Rotation all or part of stomach > 180 degrees, Ā± closed-loop obstruction, possible strangulation ā€¢ It is the rotation and not the obstruction which defines the presence of volvulus
  • 39. ā€¢ Organoaxial volvulus: Rotation around longitudinal axis (most common) ā€¢ Around line extending from cardia to pylorus ā€¢ Stomach twists anteriorly or posteriorly ā€¢ Antrum moves inferior to superior
  • 40. ā€¢ Mesenteroaxial volvulus: Rotation about mesenteric axis ā€¢ Axis running across stomach right angles to lesser & greater curves ā€¢ Rotation right to left or left to right about gastrohepatic omentum ā€¢ Mixed volvulus ā€¢ Combination of OAV & MAV
  • 41. Radiography ā€¢ Abdominal plain films; patient upright ā€¢ Double air-fluid level ā€¢ Large, distended stomach; spheric viscus displaced upward to left ā€¢ Elevation of diaphragm ā€¢ Small bowel collapsed; paucity distal gas ā€¢ Intramural emphysema gastric wall ā€¢ Chest X-ray ā€¢ Intrathoracic up-side down stomach ā€¢ Retrocardiac fluid level ā€¢ 2 air-fluid interfaces different heights ā€¢ Simultaneous fluid levels above & below diaphragm
  • 42.
  • 43.
  • 44. Fluoroscopic Findings ā€¢ Massively distended stomach left upper quadrant, may extending into chest ā€¢ Inversion of stomach ā€¢ Greater curvature above lesser ā€¢ Cardia & pylorus at same level ā€¢ Downward pointing pylorus & duodenum ā€¢ May see "beaking" at point of twist ā€¢ OAV: 2 points of twist; luminal obstruction ā€¢ Contrast in stomach may not pass beyond pylorus ā€¢ MAV: Antrum & pylorus lie above gastric fundus
  • 46. CT Findings ā€¢ Not generally performed for GV ā€¢ CT appearance may be variable ā€¢ Depends on extent of gastric herniation, points of torsion, position of stomach ā€¢ May be linear septum within gastric lumen (area of torsion) ā€¢ Large hiatal hernia accompanied by partial GV ā€¢ "Pseudothrombosis" of inferior vena cava on CT
  • 48. DUODENUM Duodenal Obstruction ā€¢ Complete duodenal obstruction is seen much more frequently than congenital gastric obstruction. ā€¢ Vomiting is usually delayed until after the first feeding but increases progressively thereafter
  • 49. Radiographic Appearance of Duodenal Obstruction Complete obstruction ļƒ¼ Gasless abdomen ļƒ¼ Gas in stomach and prox. duodenum ļƒ¼ Gas distally if bifid common bile duct Partial obstruction ļƒ¼ Gastric distention ļƒ¼ Distended small bowel ļƒ¼ ā€œDouble bubbleā€ ļƒ¼ Scattered gas-filled bowel loops distally ļƒ¼ Normal if vomiting decompressed stomach and duodenum
  • 50.
  • 51.
  • 52. DDX Duodenal Obstruction ā€¢ Intrinsic (Often complete obstruction) -Duodenal atresia -Duodenal stenosis -Duodenal web, diaphragm, or ā€œwind sockā€ ā€¢ Extrinsic (Often partial obstruction) -Malrotation with midgut volvulus -Malrotation with Laddā€™s bands -Annular pancreas -Preduodenal portal vein -Hematoma
  • 53. Duodenal atresia ā€¢ Most important cause of complete duodenal obstruction. ā€¢ Failure of recanalization of the duodenum between approximately the 9th and 11th weeks of gestation
  • 54.
  • 55. Jejunal atresia ā€¢ Normal or near normal size colon ā€¢ Seen in jejunal and proximal ileal atresias ā€¢ Colon receives succus entericus from remaining small bowel
  • 58. Ileal atresia - Contrast enema ā€¢ Microcolon (small unused colon) ā€¢ The earlier in gestation the obstruction occurs
  • 62. Abnormal Gut Rotation ā€¢ Nonrotation ā€¢ When both limbs return to abdomen without further rotation ā€¢ Small bowel on right and colon on left ā€¢ Wide mesentery ā€“ less risk of volvulus ā€¢ Gastroschisis; Omphalocele; Diaphragmatic Hernia ā€¢ Malrotation ā€¢ Duodenojejunal limb remains in nonrotation in the right midabdomen ā€¢ Cecocolic limb in partial rotation in the midupper abdomen fixed to abdominal wall by Ladds bands
  • 63. Malrotation - Radiography ā€¢ X ray abdomen : less informative ā€¢ Abnormal configuration of gas in right hypochondrium, the duodenal triangle suggests diagnosis ā€¢ Volvulus : ā€¢ Corkscrew sign ā€¢ Tapering of beaking of the bowel in complete obstruction ā€¢ Malrotated bowel configuration ā€¢ Distal obstruction ā€¢ Closed loop syndrome features - thick walled edematous loops with pneumatosis ā€¢ Gas less abdomen due to prolonged vomiting
  • 64.
  • 65.
  • 66. ā€¢ Upper GI series - Modality of choice ā€¢ Clearly abnormal position of duodenum (81%) ļƒ˜Duodenum and Jejunum to right of spine ļƒ˜Corkscrew duodenum and jejunum ļƒ˜DJJ low and in midline ā€¢ Unusual abnormal position of duedenum (16%) ļƒ˜ DJJ over right pedicle ļƒ˜ DJJ left of spine but low ļƒ˜ Duodenal redundency to right of spine ļƒ˜ Z shaped configuration of duodenum & Jejunum
  • 67.
  • 68.
  • 69. USG - Midgut volvulus ā€¢ Clockwise whirlpool sign ā€¢ Abnormal superior mesenteric vessels ā€¢ Inverted SMA/SMV relationship ā€¢ Solitary hyperdynamic pulsating SMA ā€¢ Truncated SMA ā€¢ Inapparent SMV ā€¢ Abnormal bowel ā€¢ Dilated duodenum proximal to obstruction ā€¢ Thickened wall of small bowel distal to obstruction ā€¢ Dilated fluid filled loops of small bowel ā€¢ Ascites
  • 70. CT ā€¢ SMV to the left of SMA in 80% ā€¢ Aplastic or hypoplastic uncinate process of pancreas ā€¢ Chylous mesentric cyst (from interference of lymphatic drainage) ā€¢ Midgut volvulus ā€¢ Whirlpool sign of twisted mesentary ā€¢ Bowel obstruction ā€¢ Free fluid / free gas in advanced cases
  • 73. Angiography ā€¢ Barber pole sign ā€“ spiralling of SMA ā€¢ Tapering or abrupt termination of mesentric vessels ā€¢ Mesentric vasoconstriction ā€¢ Prolonged contrast transit time ā€¢ Absent venous opacification ā€¢ Dilated tortures superior mesentric vein.
  • 74. INTUSSUSCEPTION ā€¢ Invagination of more proximal bowel (the intussusceptum) into lumen of more distal bowel (the intussuscipiens) in a telescope-like manner ā€¢ Most common site: ā€¢ Terminal ileum/ileocecal valve ā€¢ 90% ileocolic
  • 75. Radiography ā€¢ Soft tissue mass surrounded by a crescent of gas ā€¢ Evidence of distal small bowel obstruction ā€¢ Absence of or decreased gas in the colon ā€¢ Pneumoperitoneum ā€¢ May be normal ā€¢ Left-side-down decubitus/prone views can be helpful in showing lack of air-filled cecum
  • 76.
  • 77. Intussusception ā€¢ Meniscus sign Produced by the rounded apex of the intussusceptum protruding into the column of contrast ā€¢ Coiled spring appearance Edematous mucosal folds of the returning limb of the intussusceptum are outlined by contrast material in the lumen of the colon
  • 78.
  • 81. Pseudokidney sign / Hay fork sign USG
  • 82. Mesenteric vessels dragged between entering and returning wall of intussusceptum
  • 83. Intussusception DIFFERENTIAL DIAGNOSIS ā€¢ Normal position of sigmoid colon ā€¢ Appendicitis ā€¢ Gastroenteritis ā€¢ Ovarian pathology ā€¢ Meckel diverticulum
  • 84. MECKEL DIVERTICULUM ā€¢ Remnant of the omphalomesenteric duct ā€¢ Bleeding (when contain ectopic gastric mucosa) ā€¢ Intussusception ā€¢ Bowel obstruction ā€¢ Perforation ā€¢ Rule of 2's : ā€¢ 2% Incidence of general population ā€¢ 2 feet of ileocecal valve ā€¢ Before age 2 years
  • 85. Radiography ā€¢ Right lower quadrant mass ā€¢ Displacement of bowel loops, ā€¢ Obstruction ā€¢ Enteroliths ā€¢ May be normal
  • 86. Fluoroscopic Findings ā€¢ Barium studies show indirect evidence of mass and inflammatory changes in adjacent bowel
  • 87. Ultrasonographic Findings ā€¢ Heterogeneous echotexture mass in RLQ, may mimic appendicitis ā€¢ Thick walled tubular structure or hyperemic bowel loops in RLQ ā€¢ Inflamed Meckel diverticulum may present as a cyst
  • 88. CT Findings ā€¢ Findings very similar to appendicitis ā€¢ Thick walled blind ending structure near cecum with surrounding inflammation ā€¢ If perforated may see abscess and free air ā€¢ CT is more accurate in diagnosing Meckel diverticulum than arteriography when presenting symptom is gastrointestinal bleeding in pediatric patients
  • 89. Nuclear Medicine Findings Tc-99m pertechnetate scan ā€¢ The most specific test for Meckel diverticulum is the Tc-99m pertechnetate scan: Accuracy -90% ā€¢ Pertechnetate accumulates in mucous cells when they are in an acidic environment, in this case in ectopic gastric mucosa ā€¢ The diverticulum typically does not communicate with the bowel lumen, so the radiotracer does not appear to move downstream in bowel unless there is active bleeding
  • 90.
  • 91. MECONIUM PLUG SYNDROME ā€¢ Small left colon syndrome. ā€¢ Transient functional obstruction of the newborn colon ā€¢ Common cause of distal neonatal bowel obstruction
  • 92. Radiography ā€¢ Multiple dilated loops of bowel ā€¢ Cannot differentiate dilated large from small bowel loops in neonates ā€¢ Findings nonspecific, cannot differentiate from other causes of distal bowel
  • 93. Contrast enema ā€¢ R/S ratio usually> 1 ā€¢ Descending and sigmoid colon small in caliber ā€¢ Abrupt zone of caliber transition in region of splenic flexure ā€¢ Filling defects within colon ā€¢ Ascending and transverse colon increased in caliber ā€¢ Difficult to differentiate from long segment Hirschsprung disease ā€¢ Enema often therapeutic; passage of meconium plugs during or just after enema
  • 94.
  • 95. Small left colon syndrome ā€¢ Functional immaturity of colon ā€¢ Narrow caliber of the left colon. ā€¢ Abrupt transition at the splenic flexure. ā€¢ Multiple filling defects in the left colon are due to meconium plugs ā€¢ These infants present at 1-2 days of age with failure to pass meconium.
  • 96.
  • 97. MECONIUM ILEUS ā€¢ Neonatal obstruction of the distal ileum due to abnormally thick, tenacious meconium ā€¢ Meconium becomes inspissated and obstructs the distal ileum and is usually a manifestation of cystic fibrosis ā€¢ Presenting illness in approximately 15% of CF patients
  • 98. Radiography ā€¢ Difficult to distinguish neonatal large vs. small bowel ā€¢ Uncomplicated Type ā€¢ Multiple dilated bowel loops ā€¢ Bubbly lucencies right lower quadrant ā€¢ Few air-fluid levels (sticky meconium) ā€¢ Complicated Type ā€¢ Soft tissue mass or gas less abdomen ā€¢ Ā± Intrauterine perforation and peritonitis ā€¢ Curvilinear calcifications on peritoneal surface or lining pseudocyst
  • 100. Contrast enema ā€¢ Smallest of microcolons ā€¢ Reflux contrast into terminal ileum ā€¢ Meconium pellets in terminal ileum; not much in colon ā€¢ Can be therapeutic in uncomplicated type
  • 102. MECONIUM PERITONITIS ā€¢ Chemical peritonitis from in utero bowel perforation and peritoneal leakage of sterile meconium ā€¢ At least four types are recognised: ā€¢Fibro-adhesive ā€¢Cystic ā€¢Generalised ā€¢Healed
  • 103. Meconium peritonitis Soft tissue mass, punctate or curvilinear calcifications, ascites, dilated bowel loops
  • 104.
  • 106. AN - USG ā€¢ Highly echogenic linear or clumped foci (calcifcation ) ā€¢ Snowstorm appearance ā€¢ Abdominal circumference may be increased ā€¢ Associated anomalies such as dilated fetal bowel and/or meconium pseudocysts ā€¢ Meconium pseudocyst: Heterogeneous mass with calcified wall ā€¢ Fetal ascites and/or polyhydramnios
  • 107. NECROTIZING ENTEROCOLITIS ā€¢ Idiopathic enterocolitis ā€¢ VLBW premature infants ā€¢ Combination of infection and ischemia characterized by coagulative and hemorrhagic necrosis ā€¢ Inflammation of portions of the small and large intestine
  • 108. Location ā€¢ Most common right colon and terminal ileum ā€¢ Can occur anywhere in gastrointestinal tract
  • 109. Radiography ā€¢ Findings range from normal to suggestive to diagnostic ā€¢ Normal ā€¢ Suggestive findings ā€¢ Asymmetric bowel dilation ā€¢ Featureless "unfolded" bowel loops ā€¢ Separation of bowel loops ā€¢ Fixed configuration of bowel loops over serial films
  • 113. Portal venous gas Definitive finding: Portal venous gas Branching lucencies over the liver
  • 114. The football sign / air dome sign ā€¢ Right upper quadrant gas ā€¢ Riglerā€™s (double wall) sign ā€¢ Ligament visualization ā€¢ Inverted V sign ā€¢ Triangular air ā€¢ The cupola sign ā€¢ Football or air dome ā€¢ Scrotal air Definitive finding: Free intraperitoneal air
  • 115. Bell classification ā€¢ Stage I: Early or suspected NEC ā€¢ Nonspecific ā€¢ Scalloping/separation/unfolding bowel loops ā€¢ Asymmetric bowel distention ā€¢ Stage II: Definite NEC ā€¢ Pneumatosis intestinalis: Mucosal, serosal; not always correlating with clinical symptoms/signs ā€¢ Stage III: ā€¢ Advanced disease (perforation or impending perforation) ā€¢ PVG, free intraperitoneal air, persistent loop sign, ascites
  • 116. Fluoroscopic Findings ā€¢ Enema contraindicated in presumed acute NEC ā€¢ Mucosa permeable to water-soluble contrast and excreted into kidneys ā€¢ Stricture: ā€¢ Single or multiple ā€¢ Small bowel or colon ā€¢ Chronic complication of NEC
  • 117. Ultrasonographic Findings ā€¢ Thickened bowel wall loops ā€¢ Increased (inflamed) or decreased (infarcted) vascularity ā€¢ Ascites
  • 118. Differential diagnosis ā€¢ In the correct clinical scenario the presence of gas within bowel wall has little differential. ā€¢Pneumatosis coli ā€¢Neonatal appendicitis ā€¢Meconium ileus ā€¢Hirschsprung disease ā€¢Infectious enterocolitis
  • 119. HIRSCHSPRUNG DISEASE ā€¢ Functional obstruction of the bowel due to lack of intrinsic enteric ganglion cells ā€¢ Morphology ā€¢ Denervated colon is small, narrow, spasmodic ā€¢ Innervated more proximal bowel is dilated ā€¢ Affected portion always includes the anus and variable length of Rectum ā€¢ Continuous disease ā€¢ No proximal without distal involvement
  • 120. ā€¢ Short segment disease : ~ 75% * ā€¢ Rectal and distal sigmoid colonic involvement only ā€¢ Long segment : ~ 15% ā€¢ Typically extends to splenic flexure / transverse colon ā€¢ Total colonic aganglionosis : 2 - 13% ā€¢ Zuezler-Wilson syndrome ā€¢ Occasional extension of aganglionosis into small bowel ā€¢ Ultrashort segment disease ā€¢ 3 ā€“ 4 cm of internal anal sphincter only ā€¢ Controversial entity
  • 121. Associations ā€¢ Isolated abnormality in 70% of cases ā€¢ Down syndrome : in ~ 10% ā€¢ Neurocristopathy syndromes ā€¢ Waardenburg-Shah syndrome ā€¢ Haddad syndrome ā€¢ MEN IIa ā€¢ other non-neurocristopathy syndromes ā€¢ Aarskog syndrome ā€¢ Bardet-Biedl syndrome ā€¢ Fryns syndrome ā€¢ Pallister-Hall syndrome ā€¢ Smith-Lemli-Opitz syndrome
  • 123. Contrast enema ā€¢ Rectum smaller than sigmoid (R/S ratio < 1) ā€¢ Transition zone from abnormally small distal to dilated proximal colon ā€¢ Fasciculations or sawtooth appearance of mucosa of involved colon: Spasm ā€¢ Thickened, ulcerated colon in patients with associated colitis ā€¢ Microcolon: Total colonic disease
  • 124.
  • 125.
  • 126.
  • 127. Differential diagnosis ā€¢ Functional megarectum ā€¢ Necrotising enterocolitis ā€¢ Microcolon : appears similar to long segment / whole colon Hirschsprung disease
  • 128. Megacystis-microcolon-intestinal hypoperistalsis syndrome ā€¢ The duodenum and proximal jejunum are mildly dilated. ā€¢ Small bowel is dilated and shortened, and the colon is a microcolon ā€¢ Abundance of ganglion cells in the entire gastrointestinal tract. ā€¢ Megacystis and megaureters
  • 129.
  • 130. ANORECTAL MALFORMATION ā€¢ Abnormal separation of genitourinary system from hindgut ā€¢ Spectrum; true imperforate anus (thin membrane) to atresia distal rectum ā€¢ Classification controversial ā€¢ Anatomic: Relation of rectal pouch to pubococcygeal line ā€¢ Surgical: Prognostic and therapeutic, "Penaā€œ classification
  • 131. ā€¢ Low ā€¢ Usually visible perineal orifice; stenotic or membrane ā€¢ No GU tract communication ā€¢ Intermediate ā€¢ Usually features of high lesion ā€¢ High ā€¢ Usually rectourinary fistula in males ā€¢ Usually rectovaginal or vestibular in females ā€¢ Possible vaginal, uterine, or bladder anomalies
  • 132. PUBOCOCCYGEAL LINE: ā€¢ Line is drawn between upper and middle third of pubis to lower border of S5 ā€¢ Bowel ends just above this line are termed high malformation and below one is termed low malformation.
  • 133.
  • 134. ISCHIAL LINE ā€¢ Line drawn below parallel to the pubococcygeal line at the level of the ossified ischial bone ā€¢ Corresponds to the most proximal level of bulbous urethra ā€¢ Anomalies between this two lines are termed intermediate ā€¢ If fistulas occur, they open in the bulbous urethra in male or in to vestibule or lower part of vagina in the female.
  • 135. PIT LINE ā€¢ This line is parellal to the ischial line but one to two centimetre caudal to it. ā€¢ This marks the posteroinferior part of the bulbocavernous muscle. ā€¢ If bowel gas ended below this area Called imperforate anal membrane or low ARM
  • 136. Radiography ā€¢ Distal bowel obstruction, intraluminal calcification ā€¢ Ā± Gas in bladder in males, vagina in females ā€¢ Air in rectal pouch on prone cross table lateral view: Inaccurate for level ā€¢ Bony landmark PCL ā€¢ "M" line: Horizontal to pelvis divides lower 1/3, upper 2/3 ischium ā€¢ Low lesions appear high: Meconium-packed pouch ā€¢ High lesions appear low: Straining, crying, excessive distention pouch
  • 137. ARM
  • 138. Voiding Cystourethrogram ā€¢ Catheter into cloaca (single perineal orifice) ā€¢ Enters bladder, vagina, or colon ā€¢ Bladder findings ā€¢ Normal; vesicoureteral reflux (VUR); wall- thickening; neurogenic bladder; fistula to rectum ā€¢ Urethral findings ā€¢ Opens to cloaca, fistula from rectum to posterior> bulbous> penile urethra ā€¢ Vaginal findings ā€¢ Normal; rectovaginal fistula; congenital anomalies (septate, duplicated, etc.)
  • 139. High pressure distalcolostography ā€¢ Several months after colostomy prior to repair ā€¢ Key view is lateral ā€¢ Document connection to urethra, bladder, or vagina
  • 140. Ultrasound ā€¢ Hypoechoic rectal pouch-perineal distance ā€¢ < 10 mm: Low lesion; ā€¢ > 10-15 mm - high or intermediate ā€¢ Reliability similar to radiography with similar inaccuracies
  • 141. MR Findings ā€¢ Pelvic musculature, neorectum, and anal sphincter position/integrity ā€¢ Normal to absent levator muscle ā€¢ Normal to absent anal sphincter complex ā€¢ Muscle complex malpositioned or atrophic ā€¢ Spine ā€¢ Tethered cord, spinal dysraphism, sacral agenesis
  • 142. Urinary tract anomalies associated with ARM ā€¢ Renal agenesis ā€¢ Renal ectopia ā€¢ Megaureter ā€¢ HN (PUJ obstruction) ā€¢ VUR ā€¢ PUV ā€¢ Epispadias/Hypo ā€¢ Prune belly syn ā€¢ VATER anomaly
  • 156.
  • 157. Announcement!!! GUEST LECTURE On By Consultant Radiologist, Apollo hospitals, Madurai. Date: 12.11.2011,Saturday

Editor's Notes

  1. Multiple Vertebral fusion abnormalities Congenital heart disease (VSD) Trache-oEsphageal fistula with oesophageal atresia plus rib fusion abnormalities and duodenal atresia. The gas is thought to have passed into the distal bowel by bypassing the duodenal atresia via the accessory pancreatic duct and into the ampulla.
  2. Complete esophageal duplication in a 27-year-old man with a history of dysphagia and choking. Esophagogram shows the duplicated esophagus (d) located posterior to the normal esophagus. (9) Duplication cyst in a 2-year-old girl with recurrent episodes of vomiting. (a) Esophagogram shows extrinsic compression of the left wall of the esophagus (arrows). (b) On a coronal T1-weighted MR image, a sharply defined low-signal-intensity mass (arrows) is seen adjacent to the left side of the esophagus. The mass had very high signal intensity on a T2-weighted MR image (not shown).
  3. triple-bubble appearance
  4. Corkscrew sign Malrotation with midgut volvulus in an infant. Spot film from a single contrast barium study demonstrates a corkscrew appearance of the fourth portion of the duodenum and the proximal jejunum and an abnormal position of the duodenojejunal junction.
  5. triple-bubble appearance
  6. Corkscrew sign Malrotation with midgut volvulus in an infant. Spot film from a single contrast barium study demonstrates a corkscrew appearance of the fourth portion of the duodenum and the proximal jejunum and an abnormal position of the duodenojejunal junction.