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Diaphragmatic Hernia
Thorsang Chayovan
Chaiyapongse Tangsittitum
PGY2 Radiology
Outline
• Anatomy
• Embryology
• Anatomic variants
• Diaphragmatic hernias
– Congenital: Bochdalek and Morgagni hernias, along
with diaphragmatic eventration, typically originate in
utero from developmental weaknesses or defects in
the diaphragm
– Acquired: Hiatal hernias and traumatic diaphragmatic
rupture
Diaphragm: Anatomy
• Musculotendinous dome-shaped structure that
demarcates pleural and peritoneal cavities.
• The 3 muscular components converge into the
central tendon
– Pars lumbaris
– Pars costalis
– Pars sternalis
Diaphragm: Anatomy
• Gaps between muscle groups: pleura,
peritoneum, and 2 fascial layers → potential
weakness
A, Aortic hiatus; B, Bochdalek space; CT, central tendon; E, esophageal hiatus; IVC, caval hiatus; M, Morgagni
space; L, Larrey space; PC, pars costalis; PL, pars lumbaris; PS, pars sternalis.
Diaphragm: Anatomy
• Innervation:
– Bilateral phrenic nerves (C3–C5)
– Lower intercostal nerves
• Arterial supply
– Internal thoracic artery
• Pericardiophrenic aa.
• Musculophrenic aa.
– Inferior phrenic arteries
Diaphragm: Embryology
Imaging of diaphragm
– Anatomic: All modalities
– Functional: Fluoroscopy, US, and MR fluoroscopy
Imaging of diaphragm: Radiography
• Normal
– Upper aspect: can see on frontal and lateral views
– Lower border: blend with the soft tissues
• Frontal
– Rt. dome: anterior sixth rib
– Lt. dome: usually 1 ICS lower than Rt.
• Lateral
– Anterior part of Lt. dome: obscured by cardiac shadow
– Rt. Hemidiaphragm: entirely seen
Imaging of diaphragm: Ultrasonography
• Thick echogenic line
• Portions of both domes can be seen together
on an oblique transverse subxiphoid view
obtained at midline: real-time assessment of
the movement
• Individual domes can be assessed in
parasagittal or coronal planes
Imaging of diaphragm: CT and MRI
• Excellent modalities(multiplanar capability
and soft-tissue resolution)
• Multiplanar imaging: easier understanding of the
orientation of anatomy and pathology
• MRI: excellent soft-tissue resolution
– Low signal intensity compared to skeletal muscles
in all sequences
Imaging of diaphragm: CT and MRI
• Small children: crura are larger relative to
body size and T12 vertebral body diameter +
more chance of nodularity
Anatomic Variations
• Diaphragmatic slip
• Nodular crura
• Prominent (hypertrophic) median and lateral
arcuate ligaments
Anatomic Variations: Diaphragmatic slip
• Common anatomic variant
• Folds or bundles of muscle run obliquely along
inferior surface of diaphragm → fold or strip of
muscle bundle protruding from inferior
surface of diaphragm ± smooth indentation of
liver or spleen
• Unilateral or bilateral, single or multiple
• Mimic mass, peritoneal implant, or LN
Anatomic Variations: Diaphragmatic slip
• CT:
– Hypodense bands running obliquely along the inner
surface of the diaphragm
– Scalloped appearance diaphragm
– Diaphragm tends to bulge upward on either side of slips:
mimic diaphragmatic hernia or weakness
• USG:
– Echogenic(mimic intrahepatic mass)
– Deep inspiration increased prominence of the slips.
– Care must be taken to distinguish this normal anatomic
variant from the array of true diaphragmatic defects.
Anatomic Variations: Nodular crura
• Hypertrophy or nodularity, especially in small
children and during deep inspiration
Anatomic Variations: Prominent
median and lateral arcuate ligaments
• 10%–24% of people
• Median arcuate ligament cross over proximal
portion of celiac trunk → unique indentation
• Some have compressive symptoms of celiac a:
postprandial epigastric pain and weight
loss(median arcuate ligament syndrome or
celiac artery compression syndrome)
Anatomic Variations: Prominent
median and lateral arcuate ligaments
• CT or CTA
– Hooked appearance and narrowing of celiac trunk
– Rarely, lateral arcuate ligaments appears nodular:
mimic lymph nodes and peritoneal deposits
Congenital and Developemental
Pathologic Conditions
• Congenital diaphragmatic hernia
• Eventration
• Aplasia/hypoplasia/accessory diaphragm
• Rarely, diaphragmatic abnormalities may be
seen in association with congenital pulmonary
venolobar syndrome, heterotaxy, and situs
inversus
Accessory Diaphragm
• Fibromuscular membrane fused anteriorly
with the diaphragm and coursing
posterosuperiorly to join posterior chest wall
• May associated with other congenital
anomalies: extralobar pulmonary
sequestration, lobar agenesis or aplasia, and
unilateral single pulmonary vein
Accessory Diaphragm
• Part of lung which trapped below accessory
diaphragm was supplied by pulmonary vessels
and bronchi that run through hole in
accessory diaphragm
Accessory Diaphragm
Eventration
• Abnormal elevation of an intact
hemidiaphragm into chest cavity
• Thought to be due to congenital absence of
muscle fibers in region of eventration
(however, lack of thinning fibers there)
• Other causes: focal dyskinesia and weakness
from ischemia, infarct, or neuromuscular
dysfunction
• Most common location: anteromedial aspect
of Rt. Hemidiaphragm(usually occupied by
part of liver)
• DDx
– Morgagni hernia
– pericardial cyst
– paraesophageal hernia
– bronchogenic cyst
– Tumor
• Complete eventration of a hemidiaphragm:
more common in males and typically occurs
on the left side
Diaphragmatic
Hernia
Bochdalek Hernia
• Posterolateral defect
• Between pars costalis
and pars sternalis
• Malformation of the
pleuroperitoneal fold
• Failure of the
pleuroperitoneal fold
and septum
transversum to fuse
properly with intercostal
muscles
Bochdalek Hernia
• The most common CDH
• Mostly diagnosed at antenatal US or manifest
at birth with respiratory distress
• 80% occurs on the left side
Bochdalek Hernia
• Asymptomatic
• Newborn: respiratory failure
• Age > 1 month: gastrointestinal symptoms
– Rarely bowel incarceration, strangulation,
perforation, or shock.
• Hernias in this location of natural diaphragmatic
weakness may also be acquired or exacerbated
through trauma or physical exertion.
Bochdalek Hernia: imaging
• Discontinuity of the posterior or posteromedial
diaphragm
• Protrusion of
– Peritoneal or retroperitoneal fat through the defect
– Less commonly, colon, small bowel, liver, spleen, or kidney
herniation
• DDx in radiograph:
– Lipoma, lung or diaphragmatic tumors, neurogenic tumor,
intrathoracic kidney, or pulmonary sequestration.
• CT: the homogeneous fatty composition + discontinuity
of the diaphragm
Morgagni Hernia
• An anterior opening
• Sternum medially
(pars sternalis)
• Eighth rib laterally
(pars costalis)
• Failure of fusion
between the
transverse septum and
the lateral body wall
Morgagni Hernia
• 90% are right-sided
• Mostly detected in older children and adults
– Incidental
– Manifest as pulmonary infection or GI obstruction
• Anterior herniation of bowel loops on a lateral
chest radiograph
Morgagni Hernia
• Neonates: liver, bowel, or stomach
• Older children: bowel alone
• Adults: omentum is common, and only rarely with
bowel, stomach, or liver
– Women (61%)--average age of 58 years
– Men--bimodal pattern of presentation, with a first peak at
31-35 years and 50-60 years
• If bilateral  associated with pericardial defects and
chromosomal anomalies
• Predisposing conditions ~ abdominal hernias
– pregnancy, trauma, obesity, chronic constipation, and
chronic cough
Morgagni Hernia: imaging
• Radiograph: a fatty mass in the right
cardiophrenic angle
– DDx prominent epicardial fat pad, other fat-containing
masses (lipoma, teratoma, thymoma, thymolipoma,
or liposarcoma)
• Displaced curvilinear omental vessels
– Within the “mass”
– Coursing across the diaphragmatic defect
Best appreciated with coronally reformatted CT or MR
Morgagni Hernia
• Morgagni hernia may occur as a component of the
pentalogy of Cantrell
1. Omphalocoele
2. Ectopia cordis (abnormal location of heart)
3. Diaphragmatic defect
4. Pericardial defect or sternal cleft
5. Cardiovascular malformations
– ventricular septal defect (VSD)
– atrial septal defect (ASD)
– tetralogy of Fallot
– left ventricular diverticulum
Congenital diaphragmatic hernias
• Physiologic abnormalities of the lungs
• Pulmonary hypoplasia
• Pulmonary hypertension
Congenital diaphragmatic hernias
• DDx
– Bronchopulmonary foregut malformation
– Sequestration
– Congenital cystic adenomatoid malformation
– Pulmonary agenesis or hypoplasia
Acquired Diaphragmatic Hernias
• Trauma or degeneration
• Hiatal hernia
• Traumatic diaphragmatic rupture
Hiatal hernia
• 50% of diaphragmatic hernia
• Acquired: mostly
• Congenital
Hiatal Hernia
• Esophageal hiatus
• Due to stretching,
weakening, or tearing
of the
phrenoesophageal mb
• Upward dislocation of
the esophagus and
stomach
• 2 types
– Sliding-type
– Paraesophageal
Hiatal Hernia
• Incidence increases with age
• Most are asymptomatic
• About 1/5 of patients with a hiatal hernia have
associated gastro-esophageal reflux (only in
sliding hernia)
Sliding hiatal hernia: Complications
• Best characterized
on esophagogram
• Schatzki’s B ring
demarcates the GE
junction
displaced above
the diaphragm
Sliding hiatal hernia: Complications
• Large incarcerated hiatal hernias may slowly
weep blood
– Iron deficiency anemia
• Peptic esophagitis from reflux
• Discrete marginal ulcers
• Strictures
Sliding hiatal hernia: Complications
• Common association with Barrett’s esophagus
– Columnar epithelium lining the esophagus
– Acquired condition related to chronic GERD
• Patients with a Barrett’s esophagus can develop
– Ulcer
– Stricture
– Malignancy
• 30-40 times higher risk of esophageal adenocarcinoma than
the general population
Paraesophageal hiatal hernia
• All or part of the stomach enters the thorax
through a defect in the phrenoesophageal
membrane
• Alongside the esophagus
• GE junction remains in the peritoneal cavity
• Not associated with GE reflux
• Usually incarcerated
• Higher risk of gastric volvulus
Larger hiatal hernias
• Radiograph: a gastric air bubble above the
diaphragm
– in the midline on frontal view
– posterior to the heart on lateral view
• CT or MR: gastric folds pass through the hiatus
• EG junction above the diaphragm: sliding
• EG junction under the diaphragm:
paraesophageal type
Other conditions
• Intrathoracic stomach
– Cardia may still be subdiaphragmatic
– Greater curvature may be on left or right side
• Congenitally short esophagus (rare)
– Short, straight esophagus
– Stomach in thorax
– GE reflux
Hiatal hernia
• Acquired: mostly
• Congenital
– A delay in the descent of the stomach from the
chest
– Children with paraesophageal hernia
• Gastrosplenic and gastrocolic ligaments are often
absent in
• Prone to organoaxial volvulus of the stomach and
colonic herniation
Traumatic Diaphragmatic Rupture
• Blunt injury
– Trauma
– Pregnancy or labor
– Spontaneously
The defect size is typically greater than 10 cm.
• Penetrating injury
Usually less than 2 cm in length
Traumatic Diaphragmatic Rupture
Lateral impacts
• An AP elongation
• Rupture of the diaphragm
or insertion detachment
Frontal impacts
• Increase intra-abdominal
pressure abruptly
• Transmitting the impact to
the pillars of the diaphragm
• RuptureRib fracture
• Rupture of the diaphragmatic insertion
• Tears are most likely to occur at sites of structural
weakness
• within the central tendon
• junction of muscle and central tendon.
Traumatic Diaphragmatic Rupture
• Blunt traumatic diaphragmatic rupture is more
common on the left side
– The right hemidiaphragm may be relatively
protected from injury due to buffering by the liver
– Delayed presentation--more common on the right
side, can lead to complications such as bowel
strangulation
• Indicative of a high impact and is associated
with other severe injuries
Traumatic Diaphragmatic Rupture
Direct signs
• Abrupt loss of diaphragm
continuity
• No visualization of the
hemidiaphragm
• Dangling diaphragm sign
Indrect signs
• Protrusion of abdominal
content into the pleural
space
• Collar sign
• Dependent viscera sign
• Hump sign
• Elevated abdominal organs
Direct signs of diaphragmatic rupture
• Abrupt loss of diaphragm continuity
– Associated with a thickening of the free edge due
to retraction or hemorrhage
– Spotted when the defect is small or in contact
with the abdominal fat or the aerated lung.
– This sign has a sensitivity ranging from 17 to 80%,
with a specificity of 90 to 100%.
Direct signs of diaphragmatic rupture
• No visualization of the hemidiaphragm
– Large hernial defects
– This sign has a specificity of 91% and a sensitivity
ranging from 18 to 43%
Direct signs of diaphragmatic rupture
• Dangling diaphragm sign
– A comma-shaped curving of the free edge at the
rupture site
– This sign has a specificity of 98% and a sensitivity
of 54%
Traumatic Diaphragmatic Rupture
Direct signs
• Abrupt loss of diaphragm
continuity
• No visualization of the
hemidiaphragm
• Dangling diaphragm sign
Indirect signs
• Protrusion of abdominal
content into the pleural
space
• Collar sign
• Dependent viscera sign
• Hump sign
• Elevated abdominal organs
Indirect signs of diaphragmatic
rupture
• Protrusion of abdominal organs or peritoneal
fat into the pleural space
– This sign has a specificity of 98% and a sensitivity
ranging from 50 to 95%
Indirect signs of diaphragmatic
rupture
• Collar sign
– Secondary to the
compression of a
herniated structure at
the site of rupture
– DDx diaphragmatic
displacement, hepatic
lacerations or
artifacts caused by
breathing
Indirect signs of diaphragmatic
rupture
• Dependent viscera sign
– The herniated abdominal organ in direct contact with
the posterior thoracic wall
– Spleen, liver, stomach and intestinal loops suspended
above the diaphragm and separated from the
posterior thoracic wall by the lung parenchyma.
– Herniated abdominal viscera to slightly drop, due to
gravity, into contact with the posterior thoracic wall.
– This sign has a specificity ranging from 54 to 90% and
a sensitivity ranging from 98 to 100%.
Indirect signs of diaphragmatic
rupture
• Hump sign
– A consequence of hepatic herniation
– hypodense band in the hepatic parenchyma
between the torn diaphragm edges
(compression-driven hypoperfusion condition)
Indirect signs of diaphragmatic
rupture
• Elevated abdominal organs
– Contralateral hemidiaphragm to be at a lower
level
– Suggestive when displacement > 5 cm in the right
side and 4 cm in the left side is found
– DDx simple anatomical variation, eventration,
paralysis of the diaphragm, or presence of
subpulmonary fluid.
Summary
• Anatomic variants
– Diaphragmatic slip
– Nodular crura
– Prominent (hypertrophic) median and lateral
arcuate ligaments
Summary
• Diaphragmatic hernias
– Congenital: Bochdalek and Morgagni hernia
– Acquired: Hiatal hernia and traumatic
Diaphragmatic
Hernia
References
• Chavhan, G. B., P. S. Babyn, R. A. Cohen, and J. C. Langer.
"Multimodality Imaging of the Pediatric Diaphragm: Anatomy and
Pathologic Conditions." Radiographics 30.7 (2010): 1797-817. Web.
• Taylor, George A., Omolola M. Atalabi, and Judy A. Estroff. "Imaging
of Congenital Diaphragmatic Hernias." Pediatric Radiology 39.1
(2009): 1-16. Web.
• Gimena A. R., Jorge A. C., and Liliana A. “Traumatic Diaphragmatic
Hernia: Case Series and Topic Review.” Colomb Radiol. 2012; 23(4):
3579-86. Web.
• Desir, Amandine, and Benoît Ghaye. "CT of Blunt Diaphragmatic
Rupture." RadioGraphics 32.2 (2012): 477-98. Web.
• "Hiatal Hernia." LearningRadiology, n.d. Web. 29 Mar. 2015.

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Diaphragmatic Hernia Imaging and Anatomy

  • 2. Outline • Anatomy • Embryology • Anatomic variants • Diaphragmatic hernias – Congenital: Bochdalek and Morgagni hernias, along with diaphragmatic eventration, typically originate in utero from developmental weaknesses or defects in the diaphragm – Acquired: Hiatal hernias and traumatic diaphragmatic rupture
  • 3. Diaphragm: Anatomy • Musculotendinous dome-shaped structure that demarcates pleural and peritoneal cavities. • The 3 muscular components converge into the central tendon – Pars lumbaris – Pars costalis – Pars sternalis
  • 4.
  • 5.
  • 6. Diaphragm: Anatomy • Gaps between muscle groups: pleura, peritoneum, and 2 fascial layers → potential weakness
  • 7. A, Aortic hiatus; B, Bochdalek space; CT, central tendon; E, esophageal hiatus; IVC, caval hiatus; M, Morgagni space; L, Larrey space; PC, pars costalis; PL, pars lumbaris; PS, pars sternalis.
  • 8.
  • 9.
  • 10. Diaphragm: Anatomy • Innervation: – Bilateral phrenic nerves (C3–C5) – Lower intercostal nerves • Arterial supply – Internal thoracic artery • Pericardiophrenic aa. • Musculophrenic aa. – Inferior phrenic arteries
  • 12. Imaging of diaphragm – Anatomic: All modalities – Functional: Fluoroscopy, US, and MR fluoroscopy
  • 13. Imaging of diaphragm: Radiography • Normal – Upper aspect: can see on frontal and lateral views – Lower border: blend with the soft tissues • Frontal – Rt. dome: anterior sixth rib – Lt. dome: usually 1 ICS lower than Rt. • Lateral – Anterior part of Lt. dome: obscured by cardiac shadow – Rt. Hemidiaphragm: entirely seen
  • 14.
  • 15. Imaging of diaphragm: Ultrasonography • Thick echogenic line • Portions of both domes can be seen together on an oblique transverse subxiphoid view obtained at midline: real-time assessment of the movement • Individual domes can be assessed in parasagittal or coronal planes
  • 16.
  • 17. Imaging of diaphragm: CT and MRI • Excellent modalities(multiplanar capability and soft-tissue resolution) • Multiplanar imaging: easier understanding of the orientation of anatomy and pathology • MRI: excellent soft-tissue resolution – Low signal intensity compared to skeletal muscles in all sequences
  • 18.
  • 19. Imaging of diaphragm: CT and MRI • Small children: crura are larger relative to body size and T12 vertebral body diameter + more chance of nodularity
  • 20.
  • 21. Anatomic Variations • Diaphragmatic slip • Nodular crura • Prominent (hypertrophic) median and lateral arcuate ligaments
  • 22. Anatomic Variations: Diaphragmatic slip • Common anatomic variant • Folds or bundles of muscle run obliquely along inferior surface of diaphragm → fold or strip of muscle bundle protruding from inferior surface of diaphragm ± smooth indentation of liver or spleen • Unilateral or bilateral, single or multiple • Mimic mass, peritoneal implant, or LN
  • 23. Anatomic Variations: Diaphragmatic slip • CT: – Hypodense bands running obliquely along the inner surface of the diaphragm – Scalloped appearance diaphragm – Diaphragm tends to bulge upward on either side of slips: mimic diaphragmatic hernia or weakness • USG: – Echogenic(mimic intrahepatic mass) – Deep inspiration increased prominence of the slips. – Care must be taken to distinguish this normal anatomic variant from the array of true diaphragmatic defects.
  • 24.
  • 25.
  • 26. Anatomic Variations: Nodular crura • Hypertrophy or nodularity, especially in small children and during deep inspiration
  • 27. Anatomic Variations: Prominent median and lateral arcuate ligaments • 10%–24% of people • Median arcuate ligament cross over proximal portion of celiac trunk → unique indentation • Some have compressive symptoms of celiac a: postprandial epigastric pain and weight loss(median arcuate ligament syndrome or celiac artery compression syndrome)
  • 28. Anatomic Variations: Prominent median and lateral arcuate ligaments • CT or CTA – Hooked appearance and narrowing of celiac trunk – Rarely, lateral arcuate ligaments appears nodular: mimic lymph nodes and peritoneal deposits
  • 29.
  • 30. Congenital and Developemental Pathologic Conditions • Congenital diaphragmatic hernia • Eventration • Aplasia/hypoplasia/accessory diaphragm • Rarely, diaphragmatic abnormalities may be seen in association with congenital pulmonary venolobar syndrome, heterotaxy, and situs inversus
  • 31. Accessory Diaphragm • Fibromuscular membrane fused anteriorly with the diaphragm and coursing posterosuperiorly to join posterior chest wall • May associated with other congenital anomalies: extralobar pulmonary sequestration, lobar agenesis or aplasia, and unilateral single pulmonary vein
  • 32. Accessory Diaphragm • Part of lung which trapped below accessory diaphragm was supplied by pulmonary vessels and bronchi that run through hole in accessory diaphragm
  • 34. Eventration • Abnormal elevation of an intact hemidiaphragm into chest cavity • Thought to be due to congenital absence of muscle fibers in region of eventration (however, lack of thinning fibers there) • Other causes: focal dyskinesia and weakness from ischemia, infarct, or neuromuscular dysfunction
  • 35. • Most common location: anteromedial aspect of Rt. Hemidiaphragm(usually occupied by part of liver)
  • 36.
  • 37.
  • 38. • DDx – Morgagni hernia – pericardial cyst – paraesophageal hernia – bronchogenic cyst – Tumor
  • 39. • Complete eventration of a hemidiaphragm: more common in males and typically occurs on the left side
  • 41. Bochdalek Hernia • Posterolateral defect • Between pars costalis and pars sternalis • Malformation of the pleuroperitoneal fold • Failure of the pleuroperitoneal fold and septum transversum to fuse properly with intercostal muscles
  • 42. Bochdalek Hernia • The most common CDH • Mostly diagnosed at antenatal US or manifest at birth with respiratory distress • 80% occurs on the left side
  • 43. Bochdalek Hernia • Asymptomatic • Newborn: respiratory failure • Age > 1 month: gastrointestinal symptoms – Rarely bowel incarceration, strangulation, perforation, or shock. • Hernias in this location of natural diaphragmatic weakness may also be acquired or exacerbated through trauma or physical exertion.
  • 44. Bochdalek Hernia: imaging • Discontinuity of the posterior or posteromedial diaphragm • Protrusion of – Peritoneal or retroperitoneal fat through the defect – Less commonly, colon, small bowel, liver, spleen, or kidney herniation • DDx in radiograph: – Lipoma, lung or diaphragmatic tumors, neurogenic tumor, intrathoracic kidney, or pulmonary sequestration. • CT: the homogeneous fatty composition + discontinuity of the diaphragm
  • 45.
  • 46.
  • 47.
  • 48.
  • 49.
  • 50.
  • 51.
  • 52.
  • 53. Morgagni Hernia • An anterior opening • Sternum medially (pars sternalis) • Eighth rib laterally (pars costalis) • Failure of fusion between the transverse septum and the lateral body wall
  • 54. Morgagni Hernia • 90% are right-sided • Mostly detected in older children and adults – Incidental – Manifest as pulmonary infection or GI obstruction • Anterior herniation of bowel loops on a lateral chest radiograph
  • 55. Morgagni Hernia • Neonates: liver, bowel, or stomach • Older children: bowel alone • Adults: omentum is common, and only rarely with bowel, stomach, or liver – Women (61%)--average age of 58 years – Men--bimodal pattern of presentation, with a first peak at 31-35 years and 50-60 years • If bilateral  associated with pericardial defects and chromosomal anomalies • Predisposing conditions ~ abdominal hernias – pregnancy, trauma, obesity, chronic constipation, and chronic cough
  • 56. Morgagni Hernia: imaging • Radiograph: a fatty mass in the right cardiophrenic angle – DDx prominent epicardial fat pad, other fat-containing masses (lipoma, teratoma, thymoma, thymolipoma, or liposarcoma) • Displaced curvilinear omental vessels – Within the “mass” – Coursing across the diaphragmatic defect Best appreciated with coronally reformatted CT or MR
  • 57.
  • 58.
  • 59.
  • 60. Morgagni Hernia • Morgagni hernia may occur as a component of the pentalogy of Cantrell 1. Omphalocoele 2. Ectopia cordis (abnormal location of heart) 3. Diaphragmatic defect 4. Pericardial defect or sternal cleft 5. Cardiovascular malformations – ventricular septal defect (VSD) – atrial septal defect (ASD) – tetralogy of Fallot – left ventricular diverticulum
  • 61. Congenital diaphragmatic hernias • Physiologic abnormalities of the lungs • Pulmonary hypoplasia • Pulmonary hypertension
  • 62.
  • 63. Congenital diaphragmatic hernias • DDx – Bronchopulmonary foregut malformation – Sequestration – Congenital cystic adenomatoid malformation – Pulmonary agenesis or hypoplasia
  • 64. Acquired Diaphragmatic Hernias • Trauma or degeneration • Hiatal hernia • Traumatic diaphragmatic rupture
  • 65. Hiatal hernia • 50% of diaphragmatic hernia • Acquired: mostly • Congenital
  • 66. Hiatal Hernia • Esophageal hiatus • Due to stretching, weakening, or tearing of the phrenoesophageal mb • Upward dislocation of the esophagus and stomach • 2 types – Sliding-type – Paraesophageal
  • 67. Hiatal Hernia • Incidence increases with age • Most are asymptomatic • About 1/5 of patients with a hiatal hernia have associated gastro-esophageal reflux (only in sliding hernia)
  • 68. Sliding hiatal hernia: Complications • Best characterized on esophagogram • Schatzki’s B ring demarcates the GE junction displaced above the diaphragm
  • 69. Sliding hiatal hernia: Complications • Large incarcerated hiatal hernias may slowly weep blood – Iron deficiency anemia • Peptic esophagitis from reflux • Discrete marginal ulcers • Strictures
  • 70. Sliding hiatal hernia: Complications • Common association with Barrett’s esophagus – Columnar epithelium lining the esophagus – Acquired condition related to chronic GERD • Patients with a Barrett’s esophagus can develop – Ulcer – Stricture – Malignancy • 30-40 times higher risk of esophageal adenocarcinoma than the general population
  • 71. Paraesophageal hiatal hernia • All or part of the stomach enters the thorax through a defect in the phrenoesophageal membrane • Alongside the esophagus • GE junction remains in the peritoneal cavity • Not associated with GE reflux • Usually incarcerated • Higher risk of gastric volvulus
  • 72.
  • 73. Larger hiatal hernias • Radiograph: a gastric air bubble above the diaphragm – in the midline on frontal view – posterior to the heart on lateral view • CT or MR: gastric folds pass through the hiatus • EG junction above the diaphragm: sliding • EG junction under the diaphragm: paraesophageal type
  • 74. Other conditions • Intrathoracic stomach – Cardia may still be subdiaphragmatic – Greater curvature may be on left or right side • Congenitally short esophagus (rare) – Short, straight esophagus – Stomach in thorax – GE reflux
  • 75.
  • 76.
  • 77. Hiatal hernia • Acquired: mostly • Congenital – A delay in the descent of the stomach from the chest – Children with paraesophageal hernia • Gastrosplenic and gastrocolic ligaments are often absent in • Prone to organoaxial volvulus of the stomach and colonic herniation
  • 78. Traumatic Diaphragmatic Rupture • Blunt injury – Trauma – Pregnancy or labor – Spontaneously The defect size is typically greater than 10 cm. • Penetrating injury Usually less than 2 cm in length
  • 79. Traumatic Diaphragmatic Rupture Lateral impacts • An AP elongation • Rupture of the diaphragm or insertion detachment Frontal impacts • Increase intra-abdominal pressure abruptly • Transmitting the impact to the pillars of the diaphragm • RuptureRib fracture • Rupture of the diaphragmatic insertion • Tears are most likely to occur at sites of structural weakness • within the central tendon • junction of muscle and central tendon.
  • 80.
  • 81. Traumatic Diaphragmatic Rupture • Blunt traumatic diaphragmatic rupture is more common on the left side – The right hemidiaphragm may be relatively protected from injury due to buffering by the liver – Delayed presentation--more common on the right side, can lead to complications such as bowel strangulation • Indicative of a high impact and is associated with other severe injuries
  • 82. Traumatic Diaphragmatic Rupture Direct signs • Abrupt loss of diaphragm continuity • No visualization of the hemidiaphragm • Dangling diaphragm sign Indrect signs • Protrusion of abdominal content into the pleural space • Collar sign • Dependent viscera sign • Hump sign • Elevated abdominal organs
  • 83. Direct signs of diaphragmatic rupture • Abrupt loss of diaphragm continuity – Associated with a thickening of the free edge due to retraction or hemorrhage – Spotted when the defect is small or in contact with the abdominal fat or the aerated lung. – This sign has a sensitivity ranging from 17 to 80%, with a specificity of 90 to 100%.
  • 84.
  • 85. Direct signs of diaphragmatic rupture • No visualization of the hemidiaphragm – Large hernial defects – This sign has a specificity of 91% and a sensitivity ranging from 18 to 43%
  • 86.
  • 87. Direct signs of diaphragmatic rupture • Dangling diaphragm sign – A comma-shaped curving of the free edge at the rupture site – This sign has a specificity of 98% and a sensitivity of 54%
  • 88.
  • 89. Traumatic Diaphragmatic Rupture Direct signs • Abrupt loss of diaphragm continuity • No visualization of the hemidiaphragm • Dangling diaphragm sign Indirect signs • Protrusion of abdominal content into the pleural space • Collar sign • Dependent viscera sign • Hump sign • Elevated abdominal organs
  • 90. Indirect signs of diaphragmatic rupture • Protrusion of abdominal organs or peritoneal fat into the pleural space – This sign has a specificity of 98% and a sensitivity ranging from 50 to 95%
  • 91.
  • 92. Indirect signs of diaphragmatic rupture • Collar sign – Secondary to the compression of a herniated structure at the site of rupture – DDx diaphragmatic displacement, hepatic lacerations or artifacts caused by breathing
  • 93.
  • 94.
  • 95. Indirect signs of diaphragmatic rupture • Dependent viscera sign – The herniated abdominal organ in direct contact with the posterior thoracic wall – Spleen, liver, stomach and intestinal loops suspended above the diaphragm and separated from the posterior thoracic wall by the lung parenchyma. – Herniated abdominal viscera to slightly drop, due to gravity, into contact with the posterior thoracic wall. – This sign has a specificity ranging from 54 to 90% and a sensitivity ranging from 98 to 100%.
  • 96.
  • 97. Indirect signs of diaphragmatic rupture • Hump sign – A consequence of hepatic herniation – hypodense band in the hepatic parenchyma between the torn diaphragm edges (compression-driven hypoperfusion condition)
  • 98.
  • 99. Indirect signs of diaphragmatic rupture • Elevated abdominal organs – Contralateral hemidiaphragm to be at a lower level – Suggestive when displacement > 5 cm in the right side and 4 cm in the left side is found – DDx simple anatomical variation, eventration, paralysis of the diaphragm, or presence of subpulmonary fluid.
  • 100.
  • 101.
  • 102.
  • 103.
  • 104.
  • 105.
  • 106. Summary • Anatomic variants – Diaphragmatic slip – Nodular crura – Prominent (hypertrophic) median and lateral arcuate ligaments
  • 107. Summary • Diaphragmatic hernias – Congenital: Bochdalek and Morgagni hernia – Acquired: Hiatal hernia and traumatic
  • 109. References • Chavhan, G. B., P. S. Babyn, R. A. Cohen, and J. C. Langer. "Multimodality Imaging of the Pediatric Diaphragm: Anatomy and Pathologic Conditions." Radiographics 30.7 (2010): 1797-817. Web. • Taylor, George A., Omolola M. Atalabi, and Judy A. Estroff. "Imaging of Congenital Diaphragmatic Hernias." Pediatric Radiology 39.1 (2009): 1-16. Web. • Gimena A. R., Jorge A. C., and Liliana A. “Traumatic Diaphragmatic Hernia: Case Series and Topic Review.” Colomb Radiol. 2012; 23(4): 3579-86. Web. • Desir, Amandine, and Benoît Ghaye. "CT of Blunt Diaphragmatic Rupture." RadioGraphics 32.2 (2012): 477-98. Web. • "Hiatal Hernia." LearningRadiology, n.d. Web. 29 Mar. 2015.