Anomalous pulmonary venous connection

Anomalous pulmonary venous connection
Illustration of total anomalous pulmonary venous connection
Specialty	Medical genetics

Anomalous pulmonary venous connection (or anomalous pulmonary venous drainage or anomalous pulmonary venous return^[1]) is a congenital heart defect of the pulmonary veins. It can be a total anomalous pulmonary venous connection, wherein all four pulmonary veins are incorrectly positioned, or a partial anomalous pulmonary venous connection, wherein only some of the pulmonary veins are incorrectly positioned.

Total anomalous pulmonary venous connection, also known as total anomalous pulmonary venous return, is a rare cyanotic congenital heart defect in which all four pulmonary veins are malpositioned and make anomalous connections to the systemic venous circulation. A right-to-left shunt such as a patent foramen ovale, patent ductus arteriosus or an atrial septal defect must be present, or else the condition is fatal due to a lack of systemic blood flow.^{[citation needed]}

In some cases, it can be detected prenatally.^[2]

There are four variants: Supracardiac (50%): blood drains to one of the innominate veins (brachiocephalic veins), azygous vein or the superior vena cava; Cardiac (20%), where blood drains into coronary sinus or directly into the right atrium; Infradiaphragmatic (20%), where blood drains into portal or hepatic veins; and a mixed (10%) variant, which can be a combination of any of the above connections.^[3]

TAPVC is further characterized on the presence or absence of obstruction, which occurs when the anomalous vein enters a vessel at an acute angle and can cause pulmonary venous hypertension and cyanosis because blood cannot enter the new vein as easily.^{[citation needed]}

The diagnosis of TAPVC is dependent upon whether or not there is an obstruction.^[4]

TAPVC with obstruction will clinically present with cyanosis, tachypnea, dyspnea, and hypoxemia. Chest x-ray may show a ground-glass appearance due to pulmonary edema resulting from increased pressure in the obstructed pulmonary veins.

Cases of TAPVC with obstruction are considered a surgical emergency.

In TAPVC without obstruction, surgical redirection can be performed within the first month of life. The operation is performed under general anesthesia. The four pulmonary veins are reconnected to the left atrium, and any associated heart defects such as atrial septal defect, ventricular septal defect, patent foramen ovale, and/or patent ductus arteriosus are surgically closed. With obstruction, surgery should be undertaken emergently. PGE1 should be given because a patent ductus arteriosus allows oxygenated blood to go from the circulation of the right heart to the systemic circulation.^{[citation needed]}

A Partial anomalous pulmonary venous connection (or Partial anomalous pulmonary venous drainage or Partial anomalous pulmonary venous return) is a congenital defect where the left atrium is the point of return for the blood from some (but not all) of the pulmonary veins.^{[citation needed]}

It is less severe than total anomalous pulmonary venous connection which is a life-threatening anomaly requiring emergent surgical correction, usually diagnosed in the first few days of life. Partial anomalous venous connection may be diagnosed at any time from birth to old age. The severity of symptoms, and thus the likelihood of diagnosis, varies significantly depending on the amount of blood flow through the anomalous connections. In less severe cases, with smaller amounts of blood flow, diagnosis may be delayed until adulthood, when it can be confused with other causes of pulmonary hypertension.^[5] There is also evidence that a significant number of mild cases are never diagnosed, or diagnosed incidentally.^[6] It is associated with other vascular anomalies, and some genetic syndromes such as Turner syndrome.^{[citation needed]}

It can be diagnosed with CT scan, angiography, transesophageal echocardiography, or cardiac MRI.^[7][8] Unfortunately, less invasive and expensive testing, such as transthoracic echocardiography and CT scanning are generally less sensitive.^{[citation needed]}

It is sometimes treated with surgery, which involves rerouting blood from the right atrium into the left atrium with a patch or use of the Warden procedure.^[9][10] However, interest is increasing in catheter-based interventional approaches, as well as medical therapy for less severe cases^{[citation needed]}.

To understand the different types of anomalous pulmonary venous connection, it is important to establish the background in which normal fetal vasculature develops.

During embryonic development, the lungs start as outgrowths from the foregut and share its splanchnic vascular plexus. At around 25 to 27 days of gestation, there are no direct links to the heart. By 27 to 29 days of gestation, the primitive pulmonary vein begins to form as an outgrowth from the left atrium and eventually connects with the primitive pulmonary venous system.

• Right ventricular heave
• Loud S1
• Fixed split S2
• S3 gallop
• Systolic ejection murmur at left upper sternal border
• Cardiomegaly
• Right ventricular hypertrophy and right axis deviation on ECG
• Snowman sign or 'figure of 8 configuration' on chest radiograph
• Right ventricular hypertrophy on echocardiogram
• Cyanosis, tachypnea, dyspnea since the overloaded pulmonary circuit can cause pulmonary edema
• Cottage-loaf sign, that is, chest X-ray appearance similar to a cottage loaf, also known as the 'snow man' sign or 'figure of 8' sign.^[11]