Total anomalous pulmonary venous return

Total anomalous pulmonary venous return (TAPVR) is a cyanotic congenital heart anomaly with abnormal drainage anatomy of the entire pulmonary venous system. This contrasts with partial anomalous pulmonary venous return (PAPVR) where only part of the pulmonary venous anatomy is abnormal.

In TAPVR, all systemic and pulmonary venous blood enters the right atrium and nothing drains into the left atrium. A right-to-left shunt is required for survival and is usually via a large patent foramen ovale (PFO) or less commonly atrial septal defect (ASD).

Affected infants develop cyanosis and congestive heart failure in the early neonatal period.

The anomaly occurs secondary to an embryological failure of pulmonary venous development:

  • at the earliest stage of lung development, the primitive lung bud venous drainage occurs via the splanchnic plexus to primitive systemic (cardinal/umbilicovitelline) veins; at this point, the heart is still forming and there is no pulmonary connection
  • at 27 to 29 days of life, a common pulmonary vein begins growing outwards from the primitive left atrium to join the primitive pulmonary veins
  • the common pulmonary vein joins with the pulmonary veins from each lung, forming the familiar configuration; simultaneously, there is involution of the primitive connection between pulmonary veins and primitive systemic veins

Failure to completely transition between primitive and mature configurations according to this sequence results in persistent venous drainage from the lungs to one of several possible systemic veins (see Classification) 4.

TAPVR can be classified into four types (in decreasing order of frequency) depending on the site of anomalous venous union 1:

  • second most common (~30% of cases)
  • pulmonary venous connection at the cardiac level
  • drainage is into the coronary sinus and then the right atrium
  • connection at the infracardiac level
  • the pulmonary veins join behind the left atrium to form a common vertical descending vein
  • the common descending vein courses anterior to the esophagus passes through the diaphragm at the esophageal hiatus and then usually join the portal system
  • drainage is usually into the ductus venosus, hepatic veins, portal vein, or IVC
  • least common type
  • anomalous venous connections at two or more levels

Approximately one-third of those with TAPVR also have other associated cardiac lesions; many have heterotaxy syndrome, particularly asplenia. Type III (infracardiac) is also associated with thoracic lymphangiectasia and pulmonary congestion.

The right heart is prominent in TAPVR because of the increased flow volume, but the left atrium remains normal in size. Types I and II result in cardiomegaly.

The supra cardiac variant (type I) can classically depict a snowman appearance on a frontal chest radiograph, also known as figure of 8 heart or cottage loaf heart 2-3. The dilated vertical vein on the left, brachiocephalic vein on top, and the superior vena cava on the right form the head of the snowman; the body of the snowman is formed by the enlarged right atrium.

May show blind-ended left atrium with no connecting veins.

Direct visualization of anomalous venous return.

Congenital heart disease

There is more than one way to present the variety of congenital heart diseases. Whichever way they are categorized, it is helpful to have a working understanding of normal and fetal circulation, as well as an understanding of the segmental approach to imaging in congenital heart disease.

Article information

rID: 7377
Synonyms or Alternate Spellings:
  • Total annomalous pulmonary venous return
  • Total anomalous pulmonary venous drainage (TAPVD)
  • Total anomalous pulmonary venous return (TAPVR)

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Cases and figures

  • Figure 1: types (diagram)
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  • Case 1
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  •  Case 1: CT
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  • Case 3: snowman sign
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  • Case 4: supracardiac
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  • Case 5: infracardiac
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  • Case 6: supracardiac type
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  • Case 7: cardiac type
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  • Case 8: infracardiac type
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  • Case 9: mixed type
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  • Case 10: infracardiac type
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  • Case 11: infracardiac (type III)
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  • Case 12
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