CASE 18123 Published on 08.05.2023

An incidental finding: Mediastinal enlargement found to be an anatomic aortic arch variant

Section

Cardiovascular

Case Type

Clinical Cases

Authors

José Juan Molina Najas

Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain

Patient

57 years, female

Categories
Area of Interest Arteries / Aorta, Cardiovascular system ; Imaging Technique CT
Clinical History

A 57-year-old woman visited the family doctor after finding a lump in her neck. Blood test results were normal. Chest x-ray showed mediastinal abnormalities, so a chest CT scan was ordered preferential to rule out lymphoma.

Imaging Findings

The chest x-ray showed an enlargement of the superior mediastinum with a rounded morphology.

A chest CT scan demonstrated a right-sided aortic arch which presented a protrusion in the origin of the left subclavian artery. This outpouching of the aorta is called Kommerell's diverticulum and is located posterior to the esophagus.

The left and right carotid arteries emerged from the ascending aorta; the right subclavian artery arose from the aortic arch's proximal segment, and the left subclavian artery appeared distally from the retro-esophageal diverticulum. The diverticulum compressed the esophagus at this level.

No cervical, supraclavicular or mediastinal adenopathies were found.

Discussion

The right aortic arch with aberrant left subclavian artery arising from a retro-esophageal diverticulum is the second most common congenital variant of the aortic arch after a double aortic arch [1,2]. Its reported prevalence is 0.04-0.4% [3].

The primitive aorta has a ventral and a dorsal segment connected by six pairs of arches. Archs progressively regress in a caudal direction.

The aortic arch variant of our case derives from the regression of the arch between the left common carotid and subclavian arteries. Kommerell's diverticulum is a remnant of the dorsal left fourth arch [2].

This anatomic variant is commonly asymptomatic, with generally no associated heart disease.

Compression of the esophagus or trachea can occur, resulting in dysphagia or dyspnea [2,3].

The diagnosis is usually casual. It is important to recognise and describe anatomic aortic variants and their relation with mediastinal structures, to avoid complications derived from possible future surgeries [4].

Treatment is generally conservative. Surgery or endovascular stent-graft replacement are reserved for cases when there is severe dysphagia; the diameter of the diverticulum orifice exceeds 3 cm, or the diameter of the descending aorta adjacent to the diverticulum is superior to 5 cm [3].

All patient data have been completely anonymised throughout the entire manuscript and related files.

Differential Diagnosis List
Right aortic arch with aberrant left subclavian artery arising from a Kommerell's diverticulum
Thoracic aorta aneurysm
Double aortic arch
Mediastinal tumors
Final Diagnosis
Right aortic arch with aberrant left subclavian artery arising from a Kommerell's diverticulum
Case information
URL: https://www.eurorad.org/case/18123
DOI: 10.35100/eurorad/case.18123
ISSN: 1563-4086
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