Pulmonary artery banding for hemi-truncus arteriosus in adulthood

N Nikolaidis1, T Velissaris, M P Haw

  • 1Wessex Cardiac Centre, Southampton University Hospital, Southampton, United Kingdom. nicnik1977@yahoo.com

Insights

Anomalous origin of the right pulmonary artery from the ascending aorta (hemi-truncus arteriosus) is rare. This case highlights a successful palliative banding procedure for an adult patient with this congenital heart defect.

Area of Science:

  • Cardiovascular Surgery
  • Congenital Heart Disease
  • Medical Case Reports

Background:

  • Anomalous origin of the right pulmonary artery from the ascending aorta, or hemi-truncus arteriosus, is a rare congenital cardiovascular malformation.
  • While typically presenting in infancy, this condition can manifest in adulthood.

Observation:

  • A 41-year-old female presented with a history of intermittent haemoptysis.
  • Cardiac catheterisation confirmed the diagnosis of hemi-truncus arteriosus.

Findings:

  • Definitive surgical correction of hemi-truncus arteriosus in adulthood carries extremely high risks.
  • A palliative right pulmonary artery banding procedure was successfully performed.

Implications:

  • Palliative right pulmonary artery banding offers a simple yet effective management strategy for adult hemi-truncus arteriosus.
  • This approach may be a viable alternative to high-risk definitive surgery in select adult cases.

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