Korean J Intern Med > Volume 39(5); 2024 > Article
Jang, Kim, Ryu, Park, and Kim: A case of esophagogastric junctional outlet obstruction caused by thoracic aortic aneurysm
An 80-year-old woman presented to the hospital with symptoms of difficulty in swallowing both solids and liquids as well as vomiting, which she had been experiencing for 6 months. In the patient’s medical history, she had long experienced a lump in the upper abdomen. She also had a history of diabetes, hyperlipidemia, and hypertension. Upper endoscopy revealed a widened esophageal lumen with fluid retention (Fig. 1A). Subsequent high-resolution manometry showed high integrated relaxation pressures of 43 mmHg (supine) and 60 mmHg (erect), with no evidence of disordered peristalsis (Fig. 1B). Esophagography findings included a narrow esophagogastric junction and delayed emptying of barium (Fig. 1C).
Chest computed tomography revealed an aortic aneurysm, with a maximum diameter of 9.5 cm, extending from the descending thoracic aorta to the upper abdominal aorta. The aneurysm was pressing the lower esophagus anteriorly (Fig. 2A, B). Consequently, the patient’s dysphagia was determined to be an esophagogastric junctional outlet obstruction secondary to compression from an aortic aneurysm. Vascular treatment was recommended; however, the patient was transferred to another hospital to explore treatment alternatives besides surgery.
Dysphagia aortica, a rare cause of secondary esophagogastric junction outlet obstruction, occurs when an aortic aneurysm externally compresses the esophagus against the left atrium [1,2]. This mechanical obstruction hinders the downward movement of the food bolus. This condition is typically associated with certain risk factors, including female sex, elderly age, hypertension, short stature, and kyphoscoliosis [3,4]. Although dysphagia aortica is uncommon, it is critical to consider it in the differential diagnosis of secondary esophagogastric junctional outflow obstruction or achalasia because of the urgent need for rapid diagnosis and effective treatment, given its association with severe complications from aortic aneurysms.

Notes

CRedit authorship contributions
Jin Ook Jang: writing - original draft; Tae Un Kim: conceptualization, supervision; Hwaseong Ryu: writing - review & editing; Byung-Soo Park: writing - review & editing; Su Jin Kim: writing - review & editing
Conflicts of interest
The authors disclose no conflicts.
Funding
This study was supported by a 2024 research grant from Pusan National University Yangsan Hospital.

Figure 1.
(A) Endoscopy shows a dilated esophageal lumen with fluid retention. (B) High-resolution manometry shows a high integrated relaxation pressure with no evidence of disordered peristalsis. (C) Esophagography shows bird peak appearance.
kjim-2024-084f1.jpg
Figure 2.
On axial (A) and coronal (B) computed tomography images, extrinsic compression of the lower esophagus (arrowheads) is demonstrated, caused by a saccular-shaped descending thoracic aortic aneurysm (arrows).
kjim-2024-084f2.jpg

REFERENCES

1. Kim JH, Jang SW, Kim DB, et al. A patient with dysphagia due to an aortic aneurysm. Korean Circ J 2009;39:258–260.
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4. Wilkinson JM, Euinton HA, Smith LF, Bull MJ, Thorpe JA. Diagnostic dilemmas in dysphagia aortica. Eur J Cardiothorac Surg 1997;11:222–227.
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