| Literature DB >> 26509033 |
Ian Reynolds1, James McGarry2, Hannan Mullett3.
Abstract
Dysphagia lusoria is present in 0.2-2.5% of the population representing the most common anomaly of the aortic arch (De Araújo et al., 2015, Int. J. Surg. Case Rep., 7, 32). It usually presents in infants, but can present at any age. Symptoms include cough, dysphagia, thoracic pain, and pulmonary infection. Barium contrast studies, CT, and MR angiography are useful studies for evaluating the condition. Dietary modification and PPI therapy are the first-line treatments with surgical intervention reserved for those with ongoing symptoms (Janssen et al., 2000, Am. J. Gastroenterol., 95, 1411).Entities:
Keywords: Aortic arch anomaly; diverticulum of Kommerell; dysphagia; dysphagia lusoria; retroesophageal subclavian artery
Year: 2015 PMID: 26509033 PMCID: PMC4614666 DOI: 10.1002/ccr3.351
Source DB: PubMed Journal: Clin Case Rep ISSN: 2050-0904
Figure 1The esophagus being compressed by the origin of the subclavian artery.
Figure 2The artery ascending in the thorax after having passed posteriorly to the esophagus.