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The persistent left superior vena cava: anatomical study, pathogenesis and clinical considerations
J Peltier1, C Destrieux, J Desme
1Laboratoire d'Anatomie, Faculté de Médecine, Université François-Rabelais, 2 bis Boulevard Tonnelé, 37032 Tours Cedex, France. jojo.peltier@caramail.com
Insights
A persistent left superior vena cava (LSVC) anomaly was found during dissection, alongside an abnormal vertebral artery origin. This cardiac anomaly can complicate venous catheterization procedures.
Area of Science:
- Cardiovascular anatomy
- Embryological development
- Vascular anomalies
Background:
- Persistence of a left superior vena cava (LSVC) is a rare congenital cardiac anomaly.
- LSVC can lead to significant complications during central venous catheterization.
- Understanding variations in venous anatomy is crucial for interventional procedures.
Observation:
- A case of LSVC was identified during anatomical dissection.
- The anomaly was associated with an aberrant origin of the vertebral artery from the aortic arch.
- The LSVC drained into the right atrium via a dilated coronary sinus ostium.
Findings:
- Detailed external and internal morphological descriptions of the LSVC and associated vertebral artery anomaly were documented.
- Embryological basis and potential variations of this anomaly were reviewed.
- Absence of azygos system abnormalities was noted.
Implications:
- The presence of LSVC poses risks during subclavian or internal jugular vein catheterization.
- Accurate anatomical knowledge is vital for preventing iatrogenic complications.
- Radiological and clinical implications for patient management are discussed.
Abstract:
The persistence of a left superior vena cava (LSVC) is an intrinsically cardiac anomaly, which can lead to serious complications during catheterization via the subclavian or internal jugular vein. We found this anomaly during dissection associated with an abnormal origin of the vertebral artery originating from the aortic arch between the left common carotid and subclavian arteries. The LSVC coursed towards the right atrium through a very dilated coronary sinus ostium. No abnormality of the azygos system was found. A thorough anatomic description was then made with external and internal morphology. The embryonic development and variations are described. Radiological and clinical implications are discussed.
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