Case Report
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World J Gastroenterol. Apr 21, 2013; 19(15): 2433-2436
Published online Apr 21, 2013. doi: 10.3748/wjg.v19.i15.2433
Dysphagia lusoria: A late onset presentation
Alice Louise Bennett, Charles Cock, Richard Heddle, Russell Kym Morcom
Alice Louise Bennett, Department of Gastroenterology and Hepatology, Flinders Medical Centre, South Australia 5042, Australia
Charles Cock, Richard Heddle, Department of Gastroenterology and Hepatology, Repatriation General Hospital, South Australia 5042, Australia
Russell Kym Morcom, Department of Radiology, Repatriation General Hospital, South Australia 5042, Australia
Author contributions: Bennett AL and Cock C were involved in the conception of the paper, data acquisition and analysis and coordinated the writing of the manuscript; Heddle R participated in the data acquisition and analysis, and contributed to the writing of the manuscript; Morcom RK participated in the data acquisition; Bennett AL, Cock C and Heddle R read and approved the final version of the manuscript.
Correspondence to: Dr. Alice Louise Bennett, Department of Gastroenterology and Hepatology, Flinders Medical Centre, Flinders Drive Bedford Park, South Australia 5042, Australia. alicebennett14@hotmail.com
Telephone: +61-8-82044964 Fax: +61-8-82042943
Received: November 7, 2012
Revised: February 19, 2013
Accepted: March 6, 2013
Published online: April 21, 2013
Abstract

Dysphagia lusoria is a term used to describe dysphagia secondary to vascular compression of the oesophagus. The various embryologic anomalies of the arterial brachial arch system often remain unrecognised and asymptomatic, but in 30%-40% of cases can result in tracheo-oesophageal symptoms, which in the majority of cases manifest as dysphagia. Diagnosis of dysphagia lusoria is via barium swallow and chest Computed tomography scan. Manometric abnormalities are variable, but age-related manometric changes may contribute to clinically relevant dysphagia lusoria in patients who present later in life. Our report describes a case of late-onset dysphagia secondary to a right aortic arch with an aberrant left subclavian artery, which represents a rare variant of dysphagia lusoria. The patient had proven additional oesophageal dysmotility with solid bolus only and a clinical response to dietary modification.

Keywords: Dysphagia, Dysphagia Lusoria, Oesophagus, Dysmotility, Endoscopy

Core tip: Dysphagia lusoria is a term used to describe dysphagia as a consequence of vascular compression of the oesophagus. Our case describes a rare anatomical variant of a right-sided aortic arch with aberrant left subclavian artery with late onset dysphagia. Manometric studies were abnormal with solid bolus, likely contributing to the worsening of the patient’s symptoms over time. The patient is managing to maintain weight and nutrition through dietary modification and no operative intervention is currently planned.