Unilateral interruption of pulmonary artery with pulmonary hypertension: a case for heart lung transplantation?
Interruption of pulmonary artery
heart lung transplantation
pulmonary hypertension
right heart failure
unilateral absence of pulmonary artery
Journal
Cardiology in the young
ISSN: 1467-1107
Titre abrégé: Cardiol Young
Pays: England
ID NLM: 9200019
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
pubmed:
1
5
2019
medline:
21
12
2019
entrez:
1
5
2019
Statut:
ppublish
Résumé
Unilateral interruption of pulmonary artery is a rare congenital anomaly which is usually associated with other congenital heart disease. Even more rarely it may occur in isolation. Most of the cases are incidentally detected in adulthood. Some cases develop pulmonary hypertension for yet unknown reasons; such cases usually present in infancy with right heart failure. Surgical correction in such cases is associated with adverse outcomes. Heart lung transplantation should be considered in such patients. We report a 3-year-old boy with interruption of right pulmonary artery with severe pulmonary hypertension and right heart failure who was considered for heart lung transplantation.
Identifiants
pubmed: 31036098
pii: S1047951119000271
doi: 10.1017/S1047951119000271
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM