A 41-year-old man with pulmonary arterial hypertension due to an inferior sinus venosus defect was referred for heart–lung transplantation. He complained of congestive heart failure and WHO 3 dyspnoea. Right ventricle ejection fraction on MRI was lowered to 18% with enlarged right cardiac cavities (end diastolic right ventricle volume: 228 ml/m2, right atrium area: 50 mm²). Under advanced pulmonary arterial hypertension therapy (tadalafil and ambrisentan), pulmonary vascular resistance was 6.2 Wood unit.m². Mean atrial pressures were highly elevated at 22 mmHg. Inferior sinus venosus defect consisted of overriding of the inferior caval vein over the interatrial septum, nicely depicted on a 3D model (panels E and F), with a large interatrial defect (panels A, B, E, and F ; star) and continuity between the inferior caval vein and the posterior wall of the left atrium (panel A). Reference Chen, Wang, Hsu, Hsu, Chen and Wu1 A prominent Eustachian valve (panel A; arrow) on the right side of the inferior caval vein directed the flow preferentially to the left atrium. An intriguing left hepatic vein anomalous return to a dilated coronary sinus was diagnosed (panels C and D). Reference Sanders2,Reference Lee and Saremi3 There was an intrahepatic small connection between the inferior caval vein and the left hepatic vein (panel D). The patient died of terminal heart failure while on the waiting list. Autopsy confirmed the diagnosis of inferior sinus venosus defect by visualising partial anomalous connection of the two right lower pulmonary veins to the inferior caval vein at its junction with the right atrium, and the anomalous drainage of the left hepatic vein to coronary sinus (panels G and H).
Left hepatic vein drainage to the coronary sinus is an extremely rare and benign congenital vascular anomaly often associated with other vascular malformations such as persistent left superior vena cava, anomalous pulmonary venous drainage, interrupted inferior caval vein with azygos continuation. Reference Morshuis, de Lind van Wijngaarden, Kik and Bogers4 In this case, its recognition was important to plan the heart–lung transplantation. Reference Vuran, Ozker, Gumus and Turkoz5,Reference Rao, Varadaraju, Girish and Singh6 Pulmonary arterial hypertension was likely to be related to the sinus venosus defect and the right ventricle volume overload. Genetic study did not identify at-risk anomaly to date. The left hepatic vein drainage to the coronary sinus was not associated with porto-caval fistula.
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