Abstract

A persistent left superior vena cava (PLSVC) is the most frequent anomaly of the venous drainage system. While both a right and left superior vena cava (SVC) are usually present, a unique, left-sided SVC, also known as an isolated PLSVC, accounts for only 10–20% of cases. It is frequently associated with arrhythmias and other congenital cardiac anomalies. Though it is usually an asymptomatic condition, it may pose significant problems whenever central venous access is needed. We report a case of an isolated PLSVC that was diagnosed incidentally during pacemaker implantation for sinus node dysfunction. The venous anomaly was associated with subvalvular aortic stenosis determined by a subaortic membrane; this particular association of congenital cardiovascular anomalies is a rare finding, with only a few cases reported in the literature. We aim to highlight the clinical and practical implications of this condition, as well as to discuss the embryonic development and diagnostic methods of this congenital defect.

Highlights

  • A persistent left superior vena cava (PLSVC), which results from the failure of obliteration of the anterior left cardinal vein during embryonic development, is the most frequent anomaly of the venous drainage system [1]

  • We report a very rare case of an isolated PLSVC associated with discrete subaortic stenosis that possible relationship between these congenital anomalies, and underline the practical implications of a was diagnosed incidentally during pacemaker implantation

  • We aimed to present this case due to the rarity of the association between an isolated PLSVC and discrete subaortic stenosis, as well as due to the various implications and learning points that derive from it

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Summary

A Case Report and Brief Review of the Literature

Irina Dems, a 1 , Daniela Cris, u 1, *, Cristian Mihai S, tefan Haba 1,2 , Andreea Maria Ursaru 1 , Vlad-Adrian Afrăsânie 3 , Irina Iuliana Costache 1,2 , Antoniu Octavian Petris, 1,2 and.

Introduction
Caseimportant
Discussion
Anatomic
Associated Congenital Anomalies
Practical
Findings
Conclusions

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