Heart Transplantation After Acute Aortic Dissection in an Adolescent With Marfan Syndrome

Ann Thorac Surg. 2022 Jun;113(6):e421-e423. doi: 10.1016/j.athoracsur.2021.08.031. Epub 2021 Sep 22.

Abstract

This report presents the case of a 14-year-old patient with clinical features of Marfan syndrome who underwent an emergency Bentall procedure for acute type A aortic dissection. The patient required postoperative extracorporeal membrane oxygenation and was listed for heart transplantation because of persistent left ventricular failure caused by an intimal tear and thrombosis of the left main coronary artery. Heart transplantation was performed 5 days after the first procedure, and the patient was discharged 60 days after admission.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Aortic Dissection* / etiology
  • Aortic Dissection* / surgery
  • Coronary Vessels
  • Heart Transplantation* / adverse effects
  • Humans
  • Marfan Syndrome* / complications
  • Marfan Syndrome* / surgery