Congenital Anomalies of Vena Caval Connection

Published on 21/06/2015 by admin

Last modified 21/06/2015

Print this page

This article have been viewed 3371 times

Chapter 29 Congenital Anomalies of Vena Caval Connection

Anomalous vena caval connections comprise a wide range of malformations that vary from minor to major and that occur in isolation or with coexisting congenital heart disease. Persistent left superior vena cava occurs in 0.3% of the general population and in 4.3% of congenital heart disease.¹ A left-sided inferior vena cava occurs in 0.2% to 0.5% of the general population.¹ This chapter focuses on isolated anomalous vena caval connections in situs solitus hearts (Table 29-1). Anomalies of vena caval connection with cardiac malpositions or with atrial isomerism are dealt with in Chapter 3.

Table 29-1 Congenital Anomalies of Vena Caval Connection

In early embryonic development, the common cardinal veins are bilaterally symmetric and are potentially responsible for bilateral superior vena cavae.² The left common cardinal vein initially drains into the left portion of the sinus venosus, which becomes the coronary sinus.² Failure of obliteration of the left common cardinal vein results in persistent connection of a left superior vena cava to the coronary sinus (Figure 29-1),² a relatively common anomaly estimated at 0.3% to 0.5% of the general population and 1.5% to 10% of patients with congenital heart disease.³ An isolated left superior vena cava in itself produces no physiologic derangements when it drains harmlessly into the right atrium via the coronary sinus (see Figure 29-1). However, the coronary sinus dilates sometimes appreciably,⁴ especially if there is atresia of its right atrial orifice⁵ or absence of the right superior vena vava.^6,⁷ When the right superior cava is absent, the sinus node pacemaker is absent because the pacemaker is normally located at the junction of the right superior vena cava and the morphologic right atrium.⁸^–¹¹ A persistent left superior vena cava is a significant anomaly when it connects to the left atrium (Figures 29-2 and 29-3).¹²^–¹⁴ The coronary sinus is usually absent¹⁵ with partial or complete unroofing of its anterosuperior wall. Unroofing results in a connection between the left atrium and the right atrium—a coronary sinus type of atrial septal defect (see Chapter 15).¹⁶ A right-to-left shunt coexists through the left superior vena caval to left atrial connection.^14,¹⁷ An absent coronary sinus with bilateral superior vena cavae (right superior cava connected to the right atrium, left superior cava connected to the left atrium) is thought to represent a developmental complex.¹⁸ If the right superior vena cava is absent or atretic (see Figure 29-3), the innominate vein crosses the midline and terminates in the left superior vena cava.¹⁹ The left atrium occasionally receives the azygos vein, the hepatic vein, or the coronary sinus,¹⁴ variations that are not considered in this chapter.

Figure 29-1 A, Persistent left superior vena cava (LSVC) draining into the right atrium (RA) via the coronary sinus. The right superior vena cava (RSVC) and the inferior vena cava (IVC) drain normally into the right atrium. B, Left superior vena cava draining into the coronary sinus in a 3-year-old child.

Figure 29-2 A, Persistent left superior vena cava (LSVC) communicating directly with the left atrium (LA). The right superior vena cava (RSVC) and the inferior vena cava (IVC) drain normally into the right atrium (RA). The bilateral superior vena cavae communicate through a large innominate bridge. The direction of blood flow is from the left atrium into the anomalous left superior vena cava and then across the innominate bridge into the right superior vena cava. These pathways constitutes a left-to-right shunt. B, Restrictive innominate bridge offers resistance so that left superior vena caval blood is diverted into the left atrium with only a small portion flowing across the bridge. C, An atretic innominate bridge diverts left superior vena caval blood entirely into the left atrium. (PV’s = pulmonary veins.)

Figure 29-3 Persistent left superior vena cava (LSVC) connecting directly to the left atrium (LA). The right superior vena cava is absent. The inferior vena cava (IVC) drains normally into the right atrium (RA).

Direct connections between vena cavae and left atrium are uncommon.^7,^20,²¹ Rarely, a right superior vena cava connects to the left atrium.²²^–²⁴ Still more rarely, a right superior vena cava connects to the left atrium, and a left superior vena cava connects to the right atrium.²⁵ Connection of a right superior vena cava to the left atrium must be distinguished from drainage of a right superior vena cava into both atria caused by a contiguous superior vena caval sinus venosus atrial septal defect (see Chapter 15).²⁰ When a right superior vena cava is congenitally absent (see Figure 29-3), brachiocephalic veins join a left superior vena cava that connects to the coronary sinus.^6,²⁶

Bilateral superior vena cavae ³ are illustrated in Figure 29-2. The innominate bridge that connects the two superior cavae may be widely patent, narrow, or atretic (see Figure 29-2), and the size of the left superior vena cava ranges from large to rudimentary.³ Bilateral superior vena cavae with atrial isomerism are dealt with in Chapter 3.

Anomalous connection of the inferior vena cava to the left atrium consists of a morphogenetic spectrum represented by combinations of persistence of the valve of the right sinus venosus, fusion of the valve with the septum secundum, and incomplete development of the atrial septum.²⁷ The inferior vena cava penetrates the diaphragm at its expected site. An enlarged azygos vein may arise from the anomalous inferior cava and convey inferior caval blood into the right atrium (Figure 29-4).^21,^28,²⁹ An isolated left-sided abdominal inferior vena cava usually crosses to the right after receiving the renal veins, then penetrates the diaphragm and enters the right atrium at the normal site. A distinction must be made between connection of the inferior vena cava to the left atrium and anomalous inferior vena caval drainage into the left atrium from persistence of a large Eustachian valve (right valve of the sinus venosus) that directs flow toward a patent foramen ovale or across an ostium secundum atrial septal defect (see Chapter 15).²⁷

Figure 29-4 Inferior vena cava (IVC) connecting directly to the left atrium (LA). An anomalous inferior vena cava gives rise to an enlarged azygos vein that joins a normal right superior vena cava (RSVC). A small portion of inferior vena caval blood is diverted through the azygos vein into the right superior vena cava and into the right atrium (RA; see curved arrow). (PV’s = pulmonary veins.)

Inferior vena caval interruption with azygous continuation is rare as an isolated malformation and is of no physiologic significance but can be mistaken for the descending thoracic aorta (Figure 29-5).³⁰ Interruption is immediately proximal to the renal veins and continues into a dilated azygos vein that enters the thorax to the right of the aorta, runs in the posterior mediastinum, and connects to a right superior vena cava (see Figure 29-5). There is an association with congenital absence of the portal vein.³¹ Inferior vena caval interruption with azygos continuation and left isomerism are dealt with in Chapter 3.

Figure 29-5 A, Inferior vena cavagram from a 28-year-old woman with isolated inferior vena caval interruption (IVC) and azygos (Az) continuation to a right superior vena cava (SVC). B, X-ray from same patient showing the azygos vein ascending along the right side of the vertebral column (lower Az) and forming a knuckle as it joins the right superior cava (upper Az).

Anomalous connection of either vena cava to the left atrium is rare enough, but connection of the right superior vena cava and the inferior vena cava to the left atrium—total anomalous systemic venous connection—is even rarer (Figures 29-6 and 29-7). ^7,^20,³² Survival depends on adequate mixing through an interatrial communication.

Figure 29-6 Electrocardiogram from a 28-year-old woman in whom the superior and inferior vena cavae both joined the left atrium—total anomalous systemic venous connection. A large ostium secundum atrial septal defect permitted interatrial mixing on which survival depended. The sinus node was absent because a junction between the superior vena cava and right atrium was absent. The P wave axis is directed upward and to the left, indicating an ectopic atrial focus. Broad notched P waves in leads 1, 3, and aVL reflect total caval drainage into the left atrium. The T wave abnormalities are nonspecific.

Figure 29-7 X-rays from the 28-year-old woman with total anomalous systemic venous connection whose electrocardiogram is shown in Figure 29-6. A, The size and configuration of the heart are normal. Pulmonary vascularity is not reduced. Increased markings in the left lower lung fields are superimposed breast tissue. B, In the lateral projection, the inferior vena caval shadow is absent (arrow).

The physiologic consequences of anomalous vena caval connections to the left atrium take into account two variables: (1), the direction and volume of blood flow through the connection; and (2), the effect of the connection on the amount of blood flow entering the right and left sides of the heart. Flow patterns are complex when a persistent left superior vena cava communicates with the left atrium (see Figure 29-2).^14,¹⁷ The left superior vena cava may be the only superior cava (see Figure 29-3), or bilateral superior cavae may fail to communicate with each other because of stenosis or atresia of the innominate bridge (see Figures 29-2B and C). All or nearly all of left superior vena caval blood is then channeled into the left atrium (Figure 29-2B and C

Buy Membership for Cardiovascular Category to continue reading. Learn more here