[Coronary-to-pulmonary artery fistulas: a report of three cases]

Murat Biçer1, Murat Yanar, Abdulkadir Ercan

  • 1Uludağ Universitesi Tip Fakültesi Kalp ve Damar Cerrahisi Anabilim Dali, Bursa, Turkey. mbicer23@yahoo.com

Insights

Congenital coronary-to-pulmonary artery fistulas are rare but can cause symptoms. Surgical repair is effective, but complex plexus-like fistulas may require reoperation.

Area of Science:

  • Cardiology
  • Thoracic Surgery
  • Congenital Heart Disease

Background:

  • Congenital coronary-to-pulmonary artery fistulas are uncommon cardiac anomalies.
  • These fistulas typically present asymptomatically.

Observation:

  • Three symptomatic patients (2 male, 1 female; aged 46-53) underwent surgical repair for coronary-to-pulmonary artery fistulas using an epicardial approach.
  • Successful repair was achieved in two patients.
  • One patient with a plexus-like fistula required reoperation under extracorporeal circulation.

Findings:

  • Direct visualization from within the pulmonary artery allowed successful closure of the fistula's distal orifice.
  • No complications or symptoms were observed during follow-up periods ranging from six months to four years.

Implications:

  • The presence of plexus-like variants in coronary-to-pulmonary artery fistulas should be considered during surgical planning.
  • Tailored treatment strategies are essential for managing complex fistula anatomies.