A fatal case of Ortner’s syndrome and dysphagia aortica secondary to rapidly expanding mycotic thoracic aortic aneurysm in a chronic kidney disease patient

Author:

Kyaw Wynn Aung1,Lim Chiao Yuen1,Khalil Muhammad Abdul Mabood1,Lim Kian Chai2,Chong Vui Heng3,Tan Jackson1

Affiliation:

1. Department of Renal Services, Hospital RIPAS, Bandar Seri Begawan, Brunei Darussalam

2. Department of Radiology, Hospital RIPAS, Bandar Seri Begawan, Brunei Darussalam

3. Department of Gastroenterology, Hospital RIPAS, Bandar Seri Begawan, Brunei Darussalam

Abstract

Ortner’s syndrome or cardiovocal syndrome is a rare condition and refers to the association between cardiovascular conditions, usually cardiac enlargement from mitral stenosis, and recurrent laryngeal nerve palsy. We reported an interesting case of a patient with end-stage renal disease on regular dialysis who developed both Ortner’s syndrome and dysphagia aortica as a result of an aortic arch aneurysm. The aneurysm underwent a rapid increase in size, likely as a result of Staphylococcus aureus infection (mycotic aneurysm) from an internal jugular dialysis catheter. This case highlighted the importance of cardiovascular conditions as rarer causes of dysphonia and dysphagia, particularly with the existence of an extrinsic infective source.

Publisher

SAGE Publications

Subject

General Medicine

Reference15 articles.

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2. Compression of the oesophagus by the aorta

3. Snell RS. Clinicalanatomy for medical student. 6th ed. Philadelphia, PA: Lippincott Williams & Wilkins, 2000, 113 pp.

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