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Aortic Arch Anomalies 
  
  Right, double, cervical aortic arch 
  
   
 
 
Right Aortic Arch 
  
General  
  - Most  are asymptomatic
 
  
    - Unless  they cause encircling vascular ring like pulmonary sling
 
   
  - Can  be complex lesions requiring multiple projections
 
  
 
Left Aortic Arch With Anomalous Right Subclavian Artery (RSCA) 
   
  - Occurs  in less than 1% of people
 
  - RSCA  passes posterior to esophagus
 
  - Pushes  trachea and esophagus forward
 
  - Produces  oblique shadow above aortic arch on frontal film
 
  - Origin  of RSCA may be dilated
 
  
    - Diverticulum  of Kommerell is most commonly seen with a right aortic arch and anomalous  left subclavian artery (LSCA)
 
   
 
 Right  Aortic Arch 
 
  - Types 
 
  
    - At  least five different types
 
    - Only  two of importance
 
    
      - Mirror  Image Type — Type I
 
      - Aberrant  left subclavian — Type II
 
     
   
 
General  considerations  
  - Recognized  by leftward displacement of barium-filled esophagus
 
  - Of  air-filled trachea
 
  - Aortic  knob is absent from left side
 
  - Aorta  descends on right
 
  - Para-aortic  stripe returns to left side of spine just above diaphragm
 
  - Mirror-image  type almost always has associated congenital heart disease (CHD) 
 
  
    - Usually  Tetralogy of Fallot 
 
   
  - Aberrant  Left Subclavian type rarely has associated CHD 
 
  
    - Most  common variety of right arch
 
   
 
Type 1—Mirror Image Type 
 
  - Secondary  to interruption of left arch just distal to ductus arteriosis
 
  - Associated  with congenital heart disease 98% of time
 
  - Imaging  Findings 
 
  
    - No  posterior impression on trachea or barium-filled esophagus
 
    - Heart  is usually abnormal in size or shape
 
    - Aorta  descends on right
 
   
 
Type ll—Aberrant Left Subclavian 
 
  - Secondary  to interruption of left aortic arch between LCC and LSC arteries
 
  - Associated  with cardiac defects 5-10% of the time
 
  
    - Tetralogy  of Fallot most often (71%)
 
    - ASD  or VSD next most often  (21%)
 
    - Coarctation  of aorta rarely (7%)
 
   
  - Anomalous  left subclavian artery (retroesophageal and  retrotracheal)
 
  - Aorta  descends on right
 
  - Imaging  Findings Right Aortic Arch with Aberrant LSCA 
 
  
    - Posterior  impression on trachea and barium-filled esophagus
 
    - Heart  is usually normal in size and shape
 
    - Aorta  descends on right
 
   
  - If  there is a mirror-image right aortic arch, then 
 
  
    - 90%  will have Tetralogy of Fallot
 
    - 6%  with Truncus Arteriosis
 
    - 5%  with Tricuspid Atresia
 
   
  - If  the person has the following lesions, then the association with a mirror-image  arch is 
 
  
    - Truncus  arteriosis                    33%      
 
    - Tetralogy  of  Fallot                  25%
 
    - Transposition                           10%
 
    - Tricuspid  atresia                      5%      
 
    - VSD                                        2%
 
   
 
Double Aortic Arch  
       
General  considerations  
  - Most  common vascular ring
 
  - Rarely  associated with congenital heart disease
 
  
    - Vascular  ring produces tracheal and/or esophageal compression
 
   
  - Caused  by persistence of R and L  IV branchial arches
 
  - Passes  on both sides of trachea
 
  - Joins  posteriorly behind esophagus
 
  - Right  arch is larger and higher
 
  - Left  arch is smaller and lower
 
  - Barium  swallow shows bilateral impressions on frontal view
 
  
    - Posterior  impression on lateral view
 
   
  - Angiogram  is characteristic
 
  - Clinical
 
  
    - Symptoms  may begin at birth and include
 
    
      - Tracheal  compression, or
 
      - Difficulty  swallowing
 
     
   
  - Anatomy
 
  
    - Right  arch supplies RSCA and RCC
 
    - Left  arch supplies LCC and LSCA
 
   
  - Double  Aortic Arch Imaging Findings 
 
  
    - Right  arch is higher and larger
 
    - Left  arch is lower and smaller
 
    - Produces  reverse S on esophagram on AP
 
    - On  lateral, arches are posterior to esophagus and anterior to trachea
 
   
 
Cervical Aortic Arch  
  - General 
 
  
    - Rare
 
    - Usually  asymptomatic
 
    - May  present as pulsating supraclavicular mass
 
    - May  produce vascular ring and compress airway
 
    - Embryogenesis  uncertain
 
    - Over  80% are right-sided
 
   
  - Imaging  Findings–Right-sided lesions 
 
  
    - Right-sided  cervical aortic arches
 
    - Right  apical mass-like density
 
    - Absence  of aortic knob on left
 
    - Aorta  descends on the left
 
    - Displace  the trachea and esophagus forward
 
    - Branching  may be normal or mirror-image
 
   
  - Imaging  Findings–Left-sided lesions 
 
  
    - Left-sided  cervical aortic arches
 
    - Aortic  knob at apex of lung
 
    - Descend  on the left
 
    - Do  not displace the trachea or esophagus forward
 
   
 
   
  
  Right Aortic Arch. The aortic knob is not visible in its normal position on the left (white arrow). The knob and descending thoracic aorta are seen on the right (red arrows). This patient did not have congenital heart disease. 
  
  
  
Right Aortic Arch. The aortic knob is not visible in its normal position on the left (redarrow). The knob (white arrow) and descending thoracic aorta (black arrows) are seen on the right. This patient did not have congenital heart disease. 
  
   
  
  
 
  
 
 
  
  
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