Journal of Chest Surgery

The Korean Society for Thoracic and Cardiovascular Surgery (대한심장혈관흉부외과학회)
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Anatomical Repair of Taussig-Bing Anomaly with Interrupted Aortic Arch and Intramural Left Coronary Artery

벽속관상동맥 기형과 대동맥궁 단절을 함께 동반한 Taussig-Bing심기형의 해부학적 완전교정

  • 성시찬 (동아대학교 의과대학 흉부외과) ;
  • 김시호 (동아대학교 의과대학 흉부외과)
  • Published : 2001.10.01
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Abstract

We report a case of the successful anatomical correction of the Taussig-Bing anomaly associated with the interrupted aortic arch and intramural left coronary artery for an 38 day-old infant Aortic arch and neoaortic reconstructions were conducted without any prosthetic or pericardial patch. Intramural left coronary was separated from right one after partial detachment of aortic commissure and both coronary artery buttons were transferred separately to the proximal main pulmonary artery(nee-aorta). Delayed sternal closure was done 3 days after the operation and hospital discharge was delayed for a month because of postoperative pneumonia. Now he is 5 months old and free of symptoms and cardiac drugs.

저자들은 벽속좌관상동맥 기형과 대동맥궁 단절을 함께 동반한 Taussig-Bing심기형을 가진 생후 39일된 환아의 해부학적 완전교정을 시행하였다. 자가심낭이나 기타 다른 보형물(Prosthesis)을 사용하지 않고 대동맥궁과 신생대동맥의 재건이 가능하였으며, 관상동맥전이 시에는, 대동맥 교련부를 부분적으로 대동맥벽으로부터 박리해 낸 후 벽속좌관상동맥을 우관상동맥으로부터 분리하여 주폐동맥의 원위부 즉 신생대동맥으로 전이하는 방법을 택하였다 술후 3일째 지연흉골봉합을 시행하였으며 폐렴으로 인해 술후 1달여간 입원가료 후 퇴원하였다 환아는 현재 5개월이며 계속적인 경구투약은 없으며 특별한 이학적 소견이나 증상은보이지 않고 있다. 벽속좌관상동맥 기형과 대동맥궁 단절을 함께 동반한 Taussig-Bing심기형의 해부학적 완전교정을 성공적으로 시행하였기에 이에 보고하는 바이다.

Keywords

References

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