Published reports and personal experience are reviewed relating to patients under 1 year of age diagnosed with a vein of Galen malformation and congenital heart disease. Including five patients from this institution, a total of 23 patients (12 neonates) with congenital heart disease and a vein of Galen malformation have been reported. Six of these had sinus venosus atrial septal defect and nine had aortic coarctation.
- vein of Galen malformation
- congenital heart disease, atrial septal defect
- coarctation of the aorta
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Vein of Galen malformations are the most common form of symptomatic cerebrovascular malformation in neonates and infants.1 Typically, newborns and young infants with a symptomatic vein of Galen malformation present with intractable heart failure, which is the most common cause of death in such patients.1 2 Although there have been isolated case reports of congenital heart disease associated with arteriovenous malformations of the cerebral circulation (table 1), there have been no comprehensive reviews of this topic. After treating a patient who had an unusual and potentially serious complication resulting from the coexistence of these conditions, we reviewed published reports and our own experience to assess the incidence and distribution of congenital heart disease in neonates and infants with vein of Galen malformations.
Patients and abnormalities
Between 1983 and 1996, 25 neonates and infants with congenital vein of Galen malformations underwent echocardiography at our institution before surgical or endovascular treatment, some of whom were included in previous reports.15 16 At the time of echocardiography, patients ranged in age from two fetuses at 36 weeks’ gestation to an 11 month old infant (median age 7 days; 19 neonates). Complete echocardiographic evaluation and head ultrasound were performed according to previously described methods.15 Patent arterial duct and patent foramen ovale were not included as congenital heart disease.
Congenital cardiovascular anomalies were identified by echocardiography in five of our 25 patients. One patient had a sinus venosus atrial septal defect with partially anomalous pulmonary venous return to the superior cavoatrial junction and two muscular ventricular septal defects; one had complete atrioventricular septal defect; one had secundum atrial septal defect; one had perimembranous ventricular septal defect with secundum atrial septal defect; and one had coarctation of the aorta. Apart from structural anomalies, mild to severe dilatation of the superior caval vein and its immediate tributaries, as well as the right sided cardiac chambers and pulmonary arteries, was observed in 21 patients.
One patient experienced an unusual complication related to the coexistence of congenital heart disease and a vein of Galen malformation. This patient was referred to our institution at 26 days old for treatment of a vein of Galen malformation fed by multiple branches of the left posterior choroidal and right pericallosal arteries (fig 1A and B). Echocardiography showed a sinus venosus atrial septal defect with anomalous drainage of the right pulmonary veins to the superior cavoatrial junction, and two small muscular ventricular septal defects. During the first stage of treatment, which consisted of transarterial embolisation of the feeding arteries, a small perforation was made in the aneurysm, which was treated by coil embolisation. During the venous phase of the procedure three days later, a single errant coil was dislodged from the malformation and embolised distally. Chest radiography and echocardiography after the procedure showed the coil to be lodged in the trabeculae of the left ventricle, directly beneath the posterior leaflet of the mitral valve (fig 2). Over the next five months, the patient underwent repair of the cardiac defects and transcatheter closure of a residual fistula into the vein of Galen malformation (fig 1C and D). At two years’ follow up the coil in the left ventricle had not shifted in location and there was no mitral valve dysfunction.
To our knowledge congenital cardiac defects associated with vein of Galen malformations have been reported in 18 patients ranging in age from 1 day to 16 months (11 neonates). Noteworthy is the concentration of cases with aortic coarctation and sinus venosus atrial septal defect (table 1). Diagnosis of cardiac disease in these 18 patients was at necropsy in 12, by echocardiography in five (four postnatal, one fetal), and by angiography in one.
Before the era of sophisticated imaging technologies and endovascular treatment, vein of Galen malformations were fatal in 90% of patients under 1 month of age and half of those between 1 month and 1 year.1 Treatment of this lesion has been revolutionised by transcatheter embolisation techniques, with 70–80% survival among neonates and young infants, and cure rates of approximately 50%.16 17 However, endovascular treatment has not been without complications, including perforation of the thin walled aneurysm or the feeding vessels (as occurred during the arterial embolisation stage in our patient), cerebral infarction, and other neurological sequelae.16 17 Another complication, sometimes fatal, has been distant migration of emboli delivered into the aneurysm by the transvenous route.17 Our patient is an unusual example of such an event, where a sinus venosus atrial septal defect allowed for paradoxical embolisation of a dislodged coil to the left ventricle. Embolisation to the distal cerebral vasculature has been reported in patients undergoing treatment for vein of Galen malformations, but in most such cases there was migration of non-absorbable liquid polymers used in particulate embolisation techniques.17
It is interesting that six of the 23 reported cases of congenital heart disease with vein of Galen malformations have been sinus venosus atrial septal defects, which are typically associated with anomalous drainage of the right pulmonary veins into the superior caval vein or right atrium. In addition, one other case had anomalous drainage of the right upper and middle pulmonary veins to the superior vena cava, which nearly always occurs with a sinus venosus atrial septal defect, although an atrial defect was not reported in this case.18Atrial septal defects constitute an estimated 7% of congenital heart defects, and sinus venosus defects comprise only 5–10% of atrial septal defects, or fewer than 1% of congenital heart defects.18
This overrepresentation of sinus venosus atrial septal defects in patients with vein of Galen malformations suggests that the association may be related to factors other than chance alone. In a report describing three patients with a vein of Galen malformation and sinus venosus atrial septal defect, Friedman et al hypothesised that increased superior caval return in utero may interfere with absorption of the right horn of the sinus venosus into the right atrium,3 which is thought to be the developmental defect involved in the formation of sinus venosus atrial septal defect with anomalous pulmonary venous drainage. From what is known about the timing of organogenesis, this hypothesis is plausible, assuming that absorption of the sinus venosus into the right atrium is completed around the eighth week of gestation, while the events responsible for formation of the vein of Galen malformation probably take place between 6 and 11 weeks’ gestation.2 Despite uncertainty regarding the nature of the association between sinus venosus atrial septal defects and vein of Galen malformations, this association may be important clinically. Unlike other types of atrial septal defect, sinus venosus defects are accompanied by a superior caval vein that overrides the septal defect, promoting direct drainage of superior caval return to the left atrium and thus facilitating paradoxical embolisation.
Another notable association was that between coarctation of the aorta and vein of Galen malformations. Nine of the 23 patients with vein of Galen malformations and congenital cardiovascular disease had either a discrete coarctation or hypoplasia of the aortic isthmus. One of the two main theories proposed to explain the development of aortic coarctation holds that increased right ventricular output in utero leads to increased flow across the arterial duct and reduced antegrade flow across the aortic isthmus.19 This is consistent with coarctation in the setting of a vein of Galen malformation, in which case low resistance in the malformation will lead to decreased antegrade flow from the ascending aorta to the isthmus. Also, cases of coarctation in patients with vein of Galen malformations—in which the coarctation has usually been described as mild—may simply reflect relative coarctation, insofar as the isthmus is the narrowest segment of the aortic arch, while the ascending aorta and transverse arch can be tremendously dilated in patients with high output distributed largely to the brain.
EVALUATION AND MANAGEMENT
A vein of Galen malformation is likely to be the dominant lesion in neonates who also have congenital heart disease. In such cases, repair or palliation of the vein of Galen malformation will almost always take priority over correction of the cardiac defects, except possibly in cardiac surgical emergencies such as obstructed total anomalous pulmonary venous return. Management of the vein of Galen malformation should not be altered because of a congenital heart defect. More thorough reports on this topic are available for detailed discussion of management.2 16 We emphasise that survival of neonates and infants with vein of Galen malformations has improved dramatically with the evolution of endovascular treatment.
Coexisting heart defects can still be critically important in the management and outcome of these patients, in part because of the potential for serious complications such as paradoxical embolisation. Thus, full echocardiographic evaluation with attention to the aortic arch and pulmonary veins is imperative. It is important to recognise the potential importance of a sinus venosus atrial septal defect (or any other shunt lesion) in the setting of a cerebral arteriovenous malformation, which leads to a high volume of systemic venous return and a large right to left shunt. Aortic coarctation varies in severity, and most cases reported with a vein of Galen malformation have been mild. Regardless of the severity of the narrowing, however, coarctation increases vascular resistance to the lower extremities and thus promotes flow through the low resistance circuit of the vein of Galen malformation. A severely symptomatic infant with such a malformation may be one of the select instances in which percutaneous dilatation of coarctation is advisable, mainly because the dilatation can be performed during the same catheterisation procedure as embolisation of the cerebral malformation. It should be recognised, however, that neonatal dilatation of coarctation has a high rate of recurrence.