A 1-year-old Maltese-Poodle mixed breed dog was referred to the cardiology service because of severe exercise intolerance and daily exercise-induced syncopal episodes. Physical examination revealed no abnormalities. Echocardiography showed intermittent underfilling of the heart. Abdominal ultrasound examination revealed a segmental aplasia of the caudal vena cava between the kidneys and the liver, and azygos continuation of the cava. The azygos vein dorsal to the right kidney showed a severe aneurysm with stasis of blood. Computed tomographic angiography showed that the right crus of the diaphragm was probably responsible for the intermittent compression of the dilated azygos vein, which was thought to have subsequently led to insufficient venous return to the heart. The underfilled ventricles could not produce sufficient cardiac output, which caused the assumed cerebral hypoperfusion due to presumed systemic arterial hypotension. Under general anesthesia a self-expanding nitinol stent was implanted into the azygos vein at the level of the diaphragm. All clinical signs resolved immediately after surgery. The dog remained free from clinical signs (6 months after surgery). This is the first report that describes the successful treatment of this congenital vascular anomaly. Ultrasonography of the caudal vena cava should be performed in dogs with unexplained syncope.
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http://dx.doi.org/10.3390/ani15050722 | DOI Listing |
Animals (Basel)
March 2025
Department of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 108, 3584 CM Utrecht, The Netherlands.
A 1-year-old Maltese-Poodle mixed breed dog was referred to the cardiology service because of severe exercise intolerance and daily exercise-induced syncopal episodes. Physical examination revealed no abnormalities. Echocardiography showed intermittent underfilling of the heart.
View Article and Find Full Text PDFIntern Med
March 2025
Department of Respiratory Medicine and Infectious Diseases, Oita University Faculty of Medicine, Japan.
J Surg Case Rep
March 2025
The Division of Thoracic Surgery, Department of Surgery, Kaiser Permanente Fontana Medical Center, 9961 Sierra Ave, Fontana, CA 92335, United States.
Azygos vein aneurysms (AVA) are rare pathologies of the thorax that can mimic a posterior mediastinal mass. Patients with AVA may be asymptomatic, or present with chest pain, pulmonary embolisms, and acute rupture. Currently, there are no standardized guidelines for treatment.
View Article and Find Full Text PDFEuropean J Pediatr Surg Rep
January 2024
Department of Dermatology, Taihe Hospital, Shiyan, Hubei, People's Republic of China.
Esophageal atresia (EA) with tracheoesophageal fistula (TEF) is a congenital anomaly that can present complex surgical challenges, especially when accompanied by rare vascular conditions like an interrupted inferior vena cava (IVC). The division of the azygos vein is a common part of TEF repair, but in the presence of an interrupted IVC, this can lead to life-threatening complications. We report the case of a newborn diagnosed with EA, TEF, and interrupted IVC, successfully treated through thoracotomy.
View Article and Find Full Text PDFBirth Defects Res
March 2025
Department of Pediatric Surgery, Dicle University, Diyarbakır, Turkey.
Background: This study aimed to develop an esophageal atresia (EA) model using fresh sheep esophagus, trachea, and lungs to simulate a realistic thoracoscopic surgical environment.
Methods: A thoracoscopic trainer box was used with fresh sheep tissues (esophagus, trachea, and lungs) to create an EA and tracheoesophageal fistula (TEF) model. The distal esophagus was anastomosed to the trachea, and a bicycle pump was integrated to simulate lung function.
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