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<p>Interrupted aortic arch (IAA) is an exceptionally rare congenital malformation (&lt; 1%), and survival into adulthood relies on the development of a robust collateral arterial network capable of sustaining distal perfusion. Its association with a stenotic bicuspid aortic valve (BAV) is uncommon. While a BAV is a common associated anomaly, its presentation with severe symptomatic stenosis in an adult with IAA is less frequently reported. We report the case of a 50-year-old male with poorly controlled arterial hypertension and heart failure, diagnosed with an IAA and a BAV.</p>

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Minimally invasive repair of interrupted aortic arch with concomitant bicuspid aortic valve disease via video-assisted left thoracotomy

  • 期刊论文

  • 发表日期：

    2026年2月26日

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  • Roger Yoel Conde Moncada,
  • Pedro Rojas Sánchez,
  • Christian Yépez Calderón,
  • Wildor Samir Cubas

摘要

Interrupted aortic arch (IAA) is an exceptionally rare congenital malformation (< 1%), and survival into adulthood relies on the development of a robust collateral arterial network capable of sustaining distal perfusion. Its association with a stenotic bicuspid aortic valve (BAV) is uncommon. While a BAV is a common associated anomaly, its presentation with severe symptomatic stenosis in an adult with IAA is less frequently reported. We report the case of a 50-year-old male with poorly controlled arterial hypertension and heart failure, diagnosed with an IAA and a BAV.