Abstract
Dysphagia lusoria is a rare disease due to an aberrant right subclavian artery that
passes posteriorly between the esophagus and the spine. David Bayford coined the term
itself meaning "freak or jest of nature" in 1761 describing a case in which the patient
had long term dysphagia that eventually led to death. Most cases of dysphagia are
due to an aberrant right subclavian artery running posterior to and causing esophageal
compression, but only 20-40% of aberrant arteries actually lead to trachea-esophageal
symptoms, including dysphagia. The majority of patients with an aberrant right subclavian
artery are asymptomatic. Treatment for dysphagia lusoria varies depending on the severity
of the symptoms. Dietary modifications are recommended in patients with mild to moderate
symptoms while vascular reconstruction is necessary for patients with severe symptoms.
We present a 44-year-old female who was diagnosed with dysphagia lusoria due to a
right-sided aortic arch and aberrant left subclavian artery (ALSA) with aneurysmal
dilation. Right aortic arch with ALSA is an uncommon arch anomaly, and only occurs
in about 0.05% of the population. Prior case reports of dysphagia lusoria differ in
that they did not report patients with an uncommon presentation of dysphagia lusoria
with aneurysmal dilatation nor was the patient diagnosed in the emergency department.
Keywords
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Article Info
Publication History
Published online: August 08, 2018
Accepted:
August 7,
2018
Received:
July 27,
2018
Footnotes
â?†Prior Presentations: None.
��Funding Sources/Disclosures: None.
â?…Conflicts of Interest: None.
Identification
Copyright
© 2018 Elsevier Inc. All rights reserved.