Dewaswala Nakeya, Bolanos Michael David, Bhopalwala Huzefa, Reda Hassan, Leventhal Andrew
Department of Cardiovascular Disease, University of Kentucky, Lexington, Kentucky.
Department of Cardiothoracic Surgery, HCA Healthcare JFK Medical Center, Atlantis, Florida.
CASE (Phila). 2024 Mar 8;8(3Part A):133-137. doi: 10.1016/j.case.2023.12.032. eCollection 2024 Mar.
• ccTGA accounts for 0.5%-1.4% of patients with congenital heart disease. • Patients with isolated ccTGA can remain undiagnosed for decades. • Very rarely, patients with ccTGA develop symptomatic AS. • Management of severe AS in patients with ccTGA presents unique challenges. • Transcatheter options are limited due to the unique anatomy.
• 矫正型大动脉转位占先天性心脏病患者的0.5%-1.4%。
• 孤立性矫正型大动脉转位患者可能数十年未被诊断。
• 矫正型大动脉转位患者极少出现有症状的主动脉狭窄。
• 矫正型大动脉转位患者严重主动脉狭窄的管理面临独特挑战。
• 由于独特的解剖结构,经导管治疗选择有限。