Is it time for a paradigm shift: Should double-lung transplant be considered the treatment of choice for idiopathic pulmonary arterial hypertension and giant pulmonary aneurysm?

J Card Surg. 2021 Aug;36(8):2996-2999. doi: 10.1111/jocs.15655. Epub 2021 May 16.

Abstract

Idiopathic pulmonary arterial hypertension is a rare condition, frequently complicated by pulmonary arteries' aneurysm. Aggressive medical therapy is often unsatisfactory and lung transplantation remains the only option. We report a unique case of severe idiopathic pulmonary arterial hypertension complicated by a giant pulmonary aneurism, massive pulmonary valve regurgitation, and right ventricle dysfunction. The patient was, as our first choice, listed for heart-lung transplantation and remained in emergency list for more than 7 months. Unfortunately, due to further clinical deterioration and the unavailability of a heart-lung bloc, plan B was mandatory. The patient underwent a combined procedure including: double lung transplant, pulmonary artery plasty, and sutureless pulmonary valve prosthesis with open deployment (first-in-man use in such scenario). Postoperative outcome was uneventful. Our thought is that double lung transplantation and conventional combined pulmonary artery/valve surgery should be considered as the first option avoiding excessive waiting times and potential further clinical deterioration.

Keywords: lung transplantation; pulmonary arterial hypertension; pulmonary artery aneurysm.

Publication types

  • Case Reports

MeSH terms

  • Aneurysm* / complications
  • Aneurysm* / diagnostic imaging
  • Aneurysm* / surgery
  • Familial Primary Pulmonary Hypertension
  • Heart-Lung Transplantation*
  • Humans
  • Lung
  • Lung Transplantation*