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An aortic aneurysm is a localized outpouching or dilation at a weak point in the artery wall. It may involve different parts of the aorta, such as the abdominal aorta, aortic arch, or thoracic aorta.Etiological factorsSeveral disorders are associated with aortic aneurysms.Congenital causes, such as primary connective tissue disorders like Marfan syndrome, impact the integrity and strength of connective tissues, notably affecting the aorta. Marfan syndrome is a genetic disorder that specifically...
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Thoracic, aortic arch and abdominal aneurysms are significant vascular conditions that can present with various clinical manifestations and lead to serious complications. Understanding these manifestations and the appropriate diagnostic studies is essential for effective management and treatment.Thoracic Aortic AneurysmsThoracic aortic aneurysms often remain asymptomatic until they reach a size that impinges on adjacent structures. They typically cause deep, diffuse chest pain that radiates to...
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Right-sided aortic arch with Kommerell's aneurysm.

Sanjay Orathi Patangi1, Rajendra Kumar Singh, Henning Pauli

  • 1Department of Cardiothoracic Anaesthesia and Intensive Care, Freeman Hospital, Newcastle Upon Tyne, United Kingdom.

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Summary

A rare Kommerell's aneurysm with a right-sided aortic arch caused progressive dysphagia in a 55-year-old woman. This case report details the management and perioperative challenges of this uncommon vascular anomaly.

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Area of Science:

  • Cardiovascular Surgery
  • Vascular Anomalies
  • Thoracic Surgery

Background:

  • Right-sided aortic arch is a rare congenital anomaly.
  • Kommerell's aneurysm is a dilatation of the proximal ascending aorta or aortic arch.
  • The combination of these two anomalies is exceptionally rare and presents unique clinical challenges.

Observation:

  • A 55-year-old female presented with progressive dysphagia.
  • Diagnostic imaging revealed a Kommerell's aneurysm associated with a right-sided aortic arch.
  • The dysphagia was attributed to extrinsic compression by the aberrant vascular structures.

Findings:

  • The patient underwent surgical intervention to address the Kommerell's aneurysm and right-sided aortic arch.
  • Management involved careful perioperative planning due to the complex anatomy.
  • Successful surgical correction was achieved, alleviating the dysphagia.

Implications:

  • This case highlights the importance of recognizing rare aortic arch anomalies.
  • Effective management requires a multidisciplinary approach and meticulous surgical technique.
  • Understanding these anomalies is crucial for improving patient outcomes in thoracic and vascular surgery.