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      Incidentally Detected Persistent Left Superior Vena Cava With an Absent Right Superior Vena Cava in a Neonate

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          Abstract

          Dear Editor, A persistent left superior vena cava with an absent right superior vena cava is extremely rare and only a few cases have been reported in adults (1-3), while no cases have been reported in neonates or infants. Here, we report a 3-week-old female who was diagnosed with this condition using transthoracic echocardiography and confirmed with thoracic computed tomography (CT) angiogram. A 3-week-old female underwent transthoracic echocardiography (iE33, Philips medical system, Andover, MA, USA) to evaluate a grade 1 systolic murmur. In the subcostal view, blood flow in the inferior vena cava drained to the right atrium, while no blood flow from the superior vena cava to the right atrium was noted (Figure 1A). In the four-chamber view, no superior vena caval blood flow was seen, but an enlarged coronary sinus drained to the right atrium. Except for a patent foramen ovale, there were no congenital heart defects. In the parasternal long-axis view, a dilated coronary sinus was noted posterior to the left atrium (Figure 1B) and the suprasternal view showed a persistent left superior vena cava with a right innominate vein draining toward the left superior vena cava and an absent right superior vena cava (Figure 1C). The baby girl was diagnosed with a persistent left superior vena cava with an absent right superior vena cava. Since there was no obvious problem with venous blood draining to the right atrium, her parents were reassured. Six months later, thoracic CT (somatome definition flash, Siemens healthcare, Forchheim, Germany) angiogram was performed to confirm the diagnosis and find any unrevealed anomalies. CT confirmed absence of the right superior vena cava and the right jugular and subclavian veins drained to the left superior vena cava through the innominate vein (Figure 2). The left superior vena cava drained to the right atrium through the dilated coronary sinus with no stenosis. The baby girl did not undergo any medical or surgical procedure to correct this anomaly and she is healthy during 2 years of follow up period. Figure 1. On Two-Dimensional Transthoracic Echocardiography A, The subcostal view shows no right superior vena cava blood flow draining to the right atrium (arrow); B, In the parasternal long axis view, an enlarged coronary sinus is seen; C, In the suprasternal view, the left superior vena cava and innominate vein are seen. AO, aorta; CS, coronary sinus; Inn V, innominate vein; LA, left atrium; LV, left ventricle. Figure 2. Three-Dimensional Computed Tomography A, Left superior vena cava draining to; B, The coronary sinus, with an absent right superior vena cava. Although a persistent left superior vena cava with a right superior vena cava is relatively common, a persistent left superior vena cava without a right superior vena cava is extremely rare. A persistent left superior vena cava with an absent right superior vena cava is generally asymptomatic, but has clinical implications. It is associated with an increased incidence of arrhythmias and conduction disturbance (4), and also has high incidence of accompanying congenital heart disease (5). Careful management is needed while inserting central venous catheter (2), cannulating in open-heart surgery (6), and also while performing electrophysiological studies and pacemaker implantation at any age (3). In neonates and infants, the subcostal and suprasternal views of echocardiography with CT images give much information on the venous anatomy which should not miss the important diagnosis. By knowing important clinical implication, future risks for patients can be expected.

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          Persistent left superior vena cava with absent right superior vena cava: a case report and review of the literature

          Summary We report on a rare case of persistent left superior vena cava (PLSVC) with absent right superior vena cava (RSVC), an anomaly that is also known as isolated PLSVC. This venous malformation was identified incidentally in a 30-year-old woman during thoracic multi-detector computed tomography (MDCT), which was performed with the suspicion of intra-thoracic malignancy. On thoracic MDCT, the RSVC was absent. A bridging vein drained the right jugular and right subclavian veins and joined the left brachiocephalic vein in order to form the PLSVC, which descended on the left side of the mediastinum and drained into the right atrium (RA) via a dilated coronary sinus (CS). The patient was referred to the cardiology department for further evaluation. Transthoracic echocardiography revealed a dilated CS, and agitated saline injected from the left or right arms revealed opacification of the CS before the RA. The patient had no additional cardiac abnormality. Isolated PLSVC is usually asymptomatic but it can pose difficulties with central venous access, pacemaker implantation and cardiothoracic surgery. This condition is also associated with an increased incidence of congenital heart disease, arrhythmias and conduction disturbances. A wide spectrum of clinicians should be aware of this anomaly, its variations and possible complications.
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            Anomalies of cardiac venous drainage associated with abnormalities of cardiac conduction system.

            The embryological development of the superior vena cava (SVC) is complex. If the left common cardinal vein fails to occlude it can, along with the left duct of Cuvier form a left SVC, which frequently drains into the coronary sinus. This may result in abnormalities in the anatomy of this structure. A persistent left SVC occurs in 0.5% of the normal population, and 3% to 4.3% of patients with congenital heart anomalies. The pacemaking tissue of the heart is derived from two sites near the progenitors of the superior vena cava. The right-sided site forms the sinoatrial node, the left-sided site is normally carried down to an area near the coronary sinus. Out of 300 patients with cardiac rhythm abnormalities, who have undergone electrophysiological studies (EPS), or permanent pacemaker insertion (PPI), we identified 12 patients with cardiac conduction abnormalities and anomalies of venous drainage. Anomalies of the coronary sinus may be associated with abnormalities of the conduction system of the heart. This may be due to the close proximity of the coronary sinus to the final position of the left-sided primitive pacemaking tissue. In our series of 300 patients, 4% had an associated left SVC, a similar incidence to that found in previous studies of congenital heart disease.
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              Left superior vena cava in pediatric cardiology associated with extra-cardiac anomalies.

              In case reports and small series, the coexistence of a persistent left superior vena cava (LSVC) and extra-cardiac anomalies has been noted. However, an association between LSVC and extra-cardiac anomalies has not been documented. We investigated the association between LSVC and extra-cardiac anomalies in patients referred to our tertiary pediatric cardiology department between 1998 and 2005. Trans-thoracic echocardiograms were performed on 4426 consecutive patients. Cardiac and extra-cardiac anomalies were registered prospectively in a computerized database. In a retrospective observational design, characteristics of patients with LSVC were collected. In 4426 patients, 1825 (41%) were diagnosed with congenital heart disease (CHD) and 295 patients (7%) with extra-cardiac anomalies. LSVC was present in 102 patients, of which 89 (87%) with CHD (OR 10.2, 95% CI 5.7 to 18.3, p<0.001) and 61 (60%) with extra-cardiac anomalies (OR 26.0, 95% CI 17.1 to 39.5, p<0.001). Confirmed syndromes were present in 43 LSVC patients (42%), including VACTERL association (vertebral defects, anal atresia, cardiac malformations, tracheo-esophageal fistula with esophageal atresia, radial and renal dysplasia, and limb anomalies, 9%), trisomy 21 (7%), 22q11 (6%) and CHARGE association (coloboma, heart defects, atresia of choanae, retardation, genital and ear anomalies, 5%). In 17 LSVC patients (17%) with multiple anomalies in different organ systems, a syndrome diagnosis was not confirmed. The LSVC appears to be indicative for both cardiac and extra-cardiac anomalies (e.g. septal defects, tetralogy of Fallot, VACTERL and CHARGE association). Disorders in the development of the secondary heart field may be causal to this combination of anomalies.
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                Author and article information

                Journal
                Iran J Pediatr
                Iran J Pediatr
                10.5812/ijp
                Kowsar
                Iranian Journal of Pediatrics
                Kowsar
                2008-2142
                2008-2150
                15 May 2016
                June 2016
                : 26
                : 3
                : e4692
                Affiliations
                [1 ]Department of Pediatrics, Chonnam National University Hospital, Gwangju, South Korea
                Author notes
                [* ]Corresponding author: Hwa Jin Cho, Department of Pediatrics, Chonnam National University Hospital, Gwangju, South Korea. Tel: +82-622206646, Fax: +82-622236103, E-mail: chhj98@ 123456gmail.com
                Article
                10.5812/ijp.4692
                4987765
                27617072
                c8e41038-e5ca-4221-b806-3effb111c7c2
                Copyright © 2016, Growth & Development Research Center

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License ( http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

                History
                : 24 November 2015
                : 08 December 2015
                Categories
                Letter

                Pediatrics
                venae cavae,echocardiography,subclavian veins
                Pediatrics
                venae cavae, echocardiography, subclavian veins

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