eMedicine Specialties > Pediatrics: Cardiac Disease and Critical Care Medicine > Cardiology

Vascular Ring, Right Aortic Arch: Differential Diagnoses & Workup

Author: Doff B McElhinney, MD, Assistant Professor of Pediatrics, Harvard Medical School; Associate in Cardiology, Department of Cardiology, Children's Hospital of Boston
Coauthor(s): Gil Wernovsky, MD, FACC, FAAP, Professor, Department of Pediatrics, University of Pennsylvania, Children's Hospital of Philadelphia
Contributor Information and Disclosures

Updated: Oct 29, 2009

Differential Diagnoses

Asthma
Pulmonary Artery Sling
Bronchiolitis
Stridor
Congenital Stridor
Tracheomalacia
Croup
Vascular Ring, Double Aortic Arch
Laryngomalacia

Other Problems to Be Considered

Laryngeal stenosis
Laryngeal web

Workup

Laboratory Studies

  • In differentiating vascular rings from upper or lower respiratory infections, a WBC count and respiratory viral studies may be helpful. However, because patients with double aortic arch are predisposed to respiratory infections, the diagnosis of an infection does not exclude the possibility of a vascular ring with a right aortic arch.
  • Because of the possible association between right aortic arch and band 22q11 deletion, a karyotype and a fluorescent in situ hybridization (FISH) test for deletions within band 22q11 may be valuable. The diagnosis of band 22q11 deletions allows for targeted evaluation and follow-up for anomalies frequently found in patients with this chromosomal anomaly.

Imaging Studies

  • Chest radiography: In patients with a vascular ring formed by a right aortic arch, chest radiography may or may not reveal the presence of a vascular ring. In the anteroposterior projection, the presence of a right aortic arch may be revealed by the location of the aortic knob and the slight leftward deviation of the lower trachea. On the lateral chest radiograph, posterior indentation of the trachea may be revealed.
  • Echocardiography: In most cases, the diagnosis of a right aortic arch with aberrant branching can be made reliably using echocardiography with the useful information obtained using suprasternal, high parasternal, and subcostal imaging. However, the presence of a vascular ring cannot always be confirmed and may be missed altogether if the ring is the form with mirror-image branching of the brachiocephalic vessels. Echocardiography is not necessary in the evaluation of patients with a suspected vascular ring if other more valuable imaging studies are available. A right aortic arch with vascular ring can also be identified on prenatal echocardiography.
  • MRI and CT scanning: MRI and CT scanning are the best single imaging studies for the diagnosis and characterization of vascular rings. They provide complete information about the arterial branching pattern, clearly reveal the locations and extent of airway and esophageal obstruction, and can be used to delineate cardiac anatomy. In addition to tomographic images, 3-dimensional reconstruction of the aorta and airways can be a useful tool for preoperative planning.
  • Cardiac catheterization: Cardiac catheterization is not usually indicated in patients with vascular ring, except when performing angiography.
  • Angiography: Although angiography was once the criterion standard for the diagnosis of rings, MRI is both less invasive and diagnostically superior. Angiography may be confusing because of the overlapping projection of the various vascular structures, if appropriate angled angiography is not performed. This problem may be somewhat ameliorated by the use of digital subtraction angiography or countercurrent brachial arteriography, which provides sequential information that can help clarify the aortic branching pattern.
  • Barium esophagography: Frequently, the diagnosis of a vascular ring is initially made with barium esophagography. In patients with a right aortic arch, a right-sided indentation of the esophagus may be observed on the anteroposterior view, depending on the tightness of the ring. Posterior indentation of the esophagus is nearly always present on the lateral view. Although this test is not necessary to make the diagnosis of a vascular ring, it is often obtained in the preliminary evaluation of patients with symptoms of upper airway and/or esophageal pathology. If a ring is strongly suspected on the basis of findings on chest radiography or echocardiography, barium esophagography is not indicated. Rather, if additional imaging is desired, a more thorough diagnostic study, such as MRI, should be performed.

Other Tests

  • ECG: No characteristic electrocardiographic findings are associated with vascular rings, and, except in patients with associated cardiovascular anomalies, electrocardiographic findings usually are normal.

Procedures

  • Diagnostic procedures are not generally necessary in the evaluation of patients with a right aortic arch.
  • Bronchoscopy may be obtained in the evaluation of a patient with suspected airway pathology but is not indicated in most patients. Pulsatile compression of the anterior and lateral walls of the trachea can be observed in patients with a vascular ring and a right aortic arch, but the specific type of vascular ring cannot always be determined. Other imaging modalities, especially MRI or CT, permit characterization of the severity and location of tracheal obstruction while offering superior definition of vascular anatomy.
  • In some cases, depending on surgeon preference, bronchoscopy may be performed in the operating room before and after repair of the vascular ring to determine the efficacy of relief of tracheal compression. This is of particular value in young patients in whom persistent tracheomalacia is a concern.

Histologic Findings

  • Histologic tissue examination is not indicated in patients with a right aortic arch.

More on Vascular Ring, Right Aortic Arch

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References

References

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Further Reading

Keywords

vascular ring, aorta, right aortic arch, trachea, esophagus, left-sided ductus arteriosus, ventricular septal defect, DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, treatment, diagnosis

Contributor Information and Disclosures

Author

Doff B McElhinney, MD, Assistant Professor of Pediatrics, Harvard Medical School; Associate in Cardiology, Department of Cardiology, Children's Hospital of Boston
Doff B McElhinney, MD is a member of the following medical societies: American Academy of Pediatrics and American College of Cardiology
Disclosure: Nothing to disclose.

Coauthor(s)

Gil Wernovsky, MD, FACC, FAAP, Professor, Department of Pediatrics, University of Pennsylvania, Children's Hospital of Philadelphia
Gil Wernovsky, MD, FACC, FAAP is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, and American Heart Association
Disclosure: Nothing to disclose.

Medical Editor

Juan Carlos Alejos, MD, Clinical Professor, Department of Pediatrics, Division of Cardiology, University of California at Los Angeles
Juan Carlos Alejos, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, American Heart Association, American Medical Association, and International Society for Heart and Lung Transplantation
Disclosure: Actelion Honoraria Speaking and teaching

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Ameeta Martin, MD, Clinical Associate Professor, Department of Pediatric Cardiology, University of Nebraska College of Medicine
Ameeta Martin, MD is a member of the following medical societies: American College of Cardiology
Disclosure: Nothing to disclose.

CME Editor

Gilbert Z Herzberg, MD, Assistant Professor, Department of Pediatrics, Section of Pediatric Cardiology, New York Medical College; Consulting Staff, Department of Pediatrics, Sound Shore Medical Center
Gilbert Z Herzberg, MD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.

Chief Editor

Steven R Neish, MD, SM, Director of Pediatric Cardiology Fellowship Program, Associate Professor, Department of Pediatrics, Baylor College of Medicine
Steven R Neish, MD, SM is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, and American Heart Association
Disclosure: Nothing to disclose.

 
 
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