Single coronary artery complicated with type A aortic dissection: a case report.

Yuji Naito, Fumitaka Suzuki, Tatsuya Murakami
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Abstract

Congenital coronary artery anomalies complicated with aortic dissection are rare. We experienced a patient with a single coronary artery presenting with a type A dissecting aortic aneurysm. A 77-year-old woman who experienced sudden back pain and was diagnosed with type A acute aortic dissection was initially treated conservatively because the false lumen thrombosed entirely. Computed tomography taken during 5 weeks of hospitalization incidentally revealed an anomalous single coronary artery arising from the left sinus of Valsalva, and the right coronary artery orifice was absent. One month after being transferred to another institution for rehabilitation, she was reintroduced to us for re-dissection of the aorta. An urgent operation involving aortic arch replacement was performed. There was a solitary coronary artery orifice at the left sinus of Valsalva and no ostium at the right sinus. The postoperative course was uneventful, and the patient was discharged 14 days after the surgery. Only 3 cases involving a single coronary artery complicated with dissecting aortic aneurysm have been reported previously.

单冠状动脉合并A型主动脉夹层1例。
先天性冠状动脉异常并主动脉夹层是罕见的。我们有一个单冠状动脉的病人,表现为a型夹层主动脉瘤。一位77岁的女性突发背部疼痛,被诊断为A型急性主动脉夹层,由于假腔完全血栓形成,最初采用保守治疗。住院5周的计算机断层扫描偶然发现一根异常的单冠状动脉起源于左Valsalva窦,右冠状动脉孔缺失。在转到其他康复机构一个月后,她被重新介绍给我们进行主动脉夹层手术。进行了主动脉弓置换术的紧急手术。左Valsalva窦有一个孤立的冠状动脉开口,右Valsalva窦无开口。术后过程顺利,患者于术后14天出院。目前仅有3例单侧冠状动脉合并夹层主动脉瘤的病例报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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