Case report: Echocardiographic and computed tomographic features of congenital bronchoesophageal artery hypertrophy and fistula in a dog
Yewon Ji, Jinsu Kang, Suyoung Heo, Kichang Lee, Hakyoung Yoon

TL;DR
This case report describes a dog with a rare abnormal blood vessel condition involving the bronchus and esophagus, diagnosed using imaging and successfully treated with surgery.
Contribution
The study presents a novel case of multi-origin systemic-to-pulmonary shunts with bronchoesophageal artery hypertrophy and fistula in a dog, including successful surgical management.
Findings
Multimodal imaging identified systemic-to-pulmonary shunts originating from multiple arteries and forming a fistula in a dog.
Surgical ligation of the shunting vessels reduced left ventricular volume overload and varices.
Postoperative imaging confirmed decreased shunt flow and improved cardiac function.
Abstract
Studies on aberrant bronchoesophageal arteries are limited. Herein, we report a case of a multi-origin systemic-to-pulmonary shunt with suspected bronchoesophageal artery hypertrophy and fistula in a dog. A 4-year-old castrated male beagle weighing 11 kg underwent routine medical screening. Physical examination revealed a right-sided continuous murmur of grades 1–2. Thoracic radiography revealed a mild cardiomegaly. Echocardiography revealed a continuous turbulent shunt flow distal to the right pulmonary artery (RPA) branch from the right parasternal short axis pulmonary artery view. Computed tomography demonstrated systemic-to-pulmonary shunts originating from the descending aorta at the level of T7–8, the right 5th and 6th dorsal intercostal arteries, and the right brachiocephalic trunk, which formed anomalous networks around the trachea and esophagus that anastomosed into a large…
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Taxonomy
TopicsCardiovascular Conditions and Treatments · Congenital Heart Disease Studies · Vascular anomalies and interventions
