Hemopericardium with cardiac tamponade as a rare presentation of a massive aortic aneurysm in a young child with autosomal recessive cutis laxa.
Khadijah MaghrabiOsman Al-RadiGaser A AbdelmohsenPublished in: Echocardiography (Mount Kisco, N.Y.) (2021)
Aortic aneurysms are rare in the pediatric age group and are commonly caused by genetic disorders associated with vasculopathy, weakness and fragility of arterial walls with progressive dilatation or even rupture. We reported a giant aortic aneurysm involving the ascending aorta and aortic arch in a 20-month-old girl with autosomal recessive cutis laxa type 1B (ARCL1B) who presented with hemorrhagic pericardial effusion and tamponade (impending rupture). Successful surgical repair has been done through excision of the aneurysmal part and replacement by Hemashield graft with preservation of the aortic valve.
Keyphrases
- aortic valve
- aortic aneurysm
- transcatheter aortic valve replacement
- transcatheter aortic valve implantation
- aortic valve replacement
- aortic stenosis
- intellectual disability
- muscular dystrophy
- multiple sclerosis
- pulmonary artery
- mental health
- left ventricular
- middle aged
- autism spectrum disorder
- case report
- copy number
- aortic dissection
- coronary artery
- gene expression
- duchenne muscular dystrophy