scholarly journals The morphogenesis and associated anomalous pulmonary venous drainage in sinus venosus defect

2020 ◽  
Vol 61 (1) ◽  
pp. 92-99
Author(s):  
Hsin-Mao Hsu ◽  
Ya-Ting Chang ◽  
Wen-Jen Su ◽  
Jaw-Ji Chu ◽  
Yu-Sheng Chang ◽  
...  
2018 ◽  
Vol 14 (8) ◽  
pp. 868-876 ◽  
Author(s):  
Mounir Riahi ◽  
Mari Nieves Velasco Forte ◽  
Nick Byrne ◽  
Anthony Hermuzi ◽  
Matthew Jones ◽  
...  

Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
Anudeep K Dodeja ◽  
Patrick I McConnell ◽  
Elisa A Bradley ◽  
Curt Daniels ◽  
Laxmi S Mehta ◽  
...  

Introduction: A dilated main pulmonary artery (MPA) seen in congenital heart disease (CHD) or pulmonary arterial hypertension (PAH) is a rare cause of angina due to left main coronary artery (LMCA) compression. Case: A 49 year old male with no prior cardiac history presented with substernal chest pain. He reported exercise intolerance for several years. On exam he had an oxygen saturation of 85%, loud P2, fixed split second heart sound and ejection click. Electrocardiogram showed right ventricular (RV) hypertrophy and no significant ST changes. Laboratory data revealed a negative troponin. An enlarged main and right pulmonary artery (RPA) (Figure 1A) was seen on computed tomography (CT) chest angiography for pulmonary embolism (CTPE) and on echocardiography he had a severely dilated RV with decreased function (Figure 1B,1C). Cardiac catheterization showed a step up in saturations from 56 to 71%, Qp:Qs of 1.5 mean MPA pressure of 53 mmHg, pulmonary capillary wedge pressure of 11mmHg and pulmonary vascular resistance (PVR) of 7WU. A slit-like narrowing of LMCA ostium was seen on coronary angiography and intravascular ultrasound (Figure 1D). He was diagnosed with a sinus venosus defect, anomalous right upper pulmonary venous drainage and suspicion for extrinsic compression of LMCA by the dilated RPA that was confirmed on cardiac CT (Figure 1E-I). He was started on triple therapy for PAH with a significant reduction in PA pressures (mean 36 mmHg and PVR 2.1 WU). Percutaneous stenting of the LMCA was deferred and he underwent successful sinus venosus defect repair with a 5mm fenestrated patch, baffling of the anomalous pulmonary veins and a 32 mm interposition graft in the MPA with reduction plasty of MPA/RPA. Conclusion: This is an unusual presentation of unrepaired CHD with angina due to a compressed LMCA from a dilated pulmonary artery. Treatment of the underlying PAH as well as repair of the defect including reduction plasty of the MPA is a consideration for symptomatic relief.


2019 ◽  
Vol 72 (12) ◽  
pp. 1088-1090
Author(s):  
Virginia Pascual-Tejerina ◽  
Ángel Sánchez-Recalde ◽  
José Ruiz Cantador ◽  
Emilio Cuesta López ◽  
Gorka Gómez-Ciriza ◽  
...  

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