A 78-year-old man presented with effort dyspnoea and oedema. He had undergone a replacement of ascending aorta for acute aortic dissection 3 years earlier, and no problems have been detected in post-operative computed tomography (CT). Echocardiogram showed a compressed right ventricle from extra-cardiac structures, resulting in right ventricular outflow tract (RVOT) stenosis and subsequent pulmonary hypertension (Panel A; Supplementary data online, Video S1). Computed tomography revealed a huge aortic pseudoaneurysm originating from peripheral anastomosis of the artificial aortic graft, which compressed the right ventricle as well as the superior vena cava, right atrium, and pulmonary artery (Panels B and C; Supplementary data online, Video S2). Additional reconstructed 3D-rendered CT clearly demonstrated that the RVOT was pinched and constricted by the aortic pseudoaneurysm (Panels D and E; Supplementary data online, Video S3). He was diagnosed with right heart failure due to compression around the RVOT by post-operative aortic pseudoaneurysm. He underwent a redo with a total arch replacement with an open stent graft to release the compression. During surgery, we found bleeding at the anastomosis between the graft and the aorta. We considered that the aortic tissue was fragile and the aortic wall would be dissected one after another by suturing haemostasis, so we added Bentall surgery. Post-operative computed tomography revealed the expanded RVOT (Panel F; Supplementary data online, Video S4) resulting in a haemodynamic normalization. He was discharged home 77 days after surgery. This is the first case of an aortic pseudoaneurysm that compressed the RVOT and led to a right heart failure.

Supplementary material

Supplementary material is available at European Heart Journal – Case Reports online.

Acknowledgements

The authors thank Yuki Iwamoto (radiologist) for technical assistance with re-construction of 3D-rendered CT imaging.

Consent: The authors confirm that written consent for submission and publication of this case report including images and associated text has been obtained from the patient in line with COPE guidance.

Funding: All authors have declared no support from any organization for the submitted work, no financial relationships with any organizations that might have an interest, and no other relationships or activities that could appear to have influenced the submitted work.

Data availability

The data underlying this article are available in the article and in its online Supplementary material.

Author notes

Conflict of interest: None declared.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Handling Editor: Can Gollmann-Tepeköylü
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