Abstract
A 10-year-old female with heterotaxy-asplenia and complex CHD developed pulmonary arteriovenous malformations with associated cyanosis after Fontan completion. She underwent orthotopic heart transplantation, but her pulmonary arteriovenous malformations persisted with progressive worsening cyanosis. Elective transcatheter left pulmonary artery embolisation was performed 2 years post-transplant, which successfully normalised her oxygen saturation without a significant increase in pulmonary artery pressure.
Original language | English |
---|---|
Pages (from-to) | 1404-1406 |
Number of pages | 3 |
Journal | Cardiology in the Young |
Volume | 29 |
Issue number | 11 |
DOIs | |
State | Published - Nov 1 2019 |
ASJC Scopus Subject Areas
- Pediatrics, Perinatology, and Child Health
- Cardiology and Cardiovascular Medicine
Keywords
- Pulmonary arteriovenous malformations
- complex CHD
- heart transplantation
- heterotaxy syndrome
- pediatrics
- pulmonary artery embolisation