# Prenatal diagnosis of absent right with persistent left superior vena cava: a case series

**Authors:** Stephen Worrall, Rahul Mital, James Strainic

PMC · DOI: 10.1007/s00246-025-03951-0 · Pediatric Cardiology · 2025-07-12

## TL;DR

This case series presents seven prenatal cases of absent right superior vena cava with persistent left superior vena cava and associated findings.

## Contribution

The study contributes a series of prenatal diagnoses of isolated persistent left superior vena cava with absent right superior vena cava and their postnatal outcomes.

## Key findings

- Seven cases of absent right superior vena cava with persistent left superior vena cava were diagnosed prenatally.
- Postnatal evaluations revealed associated cardiac anomalies and complications.
- Prenatal detection allows for monitoring and management of potential complications.

## Abstract

Persistence of a left superior vena cava (PLSVC) is the most common thoracic venous anomaly, seen in 0.3–0.5% of patients. In rare cases (0.07–0.13% of patients), however, it is associated with the absence of the right superior vena cava (RSVC), a condition known as isolated PLSVC, or IPLSVC (Kusaka et al. in JA Clin Rep, 2015; Bartram et al. in Am J Cardiol 80(2):175–183, 1997). Absent right with PLSVC itself is usually not hemodynamically significant; its discovery, however, has significant implications, specifically for future cardiac inventions such as cardiac catheterization and pacemaker placement. It is also associated with other pathologies such as coarctation of the aorta, right sided aortic arch, valvular abnormalities, and arrhythmias secondary to coronary sinus dilation (Kusaka et al. in JA Clin Rep, 2015; Bartram et al. in Am J Cardiol 80(2):175–183, 1997). For this reason, awareness of this anatomy and its variations remains critically important. It was traditionally found on autopsy or during the time of invasive cardiac procedures; but with advances in fetal echocardiography, it has become more common to be found prenatally, with an opportunity for follow-up to monitor for any complications and associated findings (Guarnier et al. in Pediatr Cardiol27(5):646–648, 2006; Kahramanoglu et al. Pediatr Cardiol 45(2):377–384, 2024). In the following series, we present the cases of seven individuals with maternal fetal echocardiographic evidence of absent right with PLSVC and associated findings on postnatal evaluation.

## Full-text entities

- **Diseases:** valvular abnormalities (MESH:D006349), coarctation of the aorta (MESH:D001017), thoracic venous anomaly (MESH:D013901), arrhythmias (MESH:D001145), PLSVC (MESH:D000083402), coronary sinus dilation (MESH:D002311)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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Source: https://tomesphere.com/paper/PMC12945967