Yokokawa Tetsuro, Watanabe Kenichi, Sakamoto Takayuki, Ohwada Takayuki, Takeishi Yasuchika
Department of Cardiology, Fukushima Red Cross Hospital, 1-31 Irietyou, Fukushima 960-8530, Japan.
Department of Cardiology and Hematology, Fukushima Medical University, 1 Hikarigaoka, Fukushima 960-1295, Japan.
J Cardiol Cases. 2012 Jul 11;6(4):e100-e102. doi: 10.1016/j.jccase.2012.06.010. eCollection 2012 Oct.
A 58-year-old woman came to our hospital because of chest pain. Multi-detector computed tomography (MDCT) showed type V dual left anterior descending artery (LAD) and a 90% stenosis in segment 1 of the right coronary artery. Two days after examination, she was admitted to our hospital because of recurrent chest pain. She was diagnosed with acute myocardial infarction. Coronary angiography showed a 99% stenosis in segment 1 and a dual LAD. She received successful percutaneous coronary intervention (PCI) to segment 1 with a bare metal stent. Type V dual LAD is a rare and complicated coronary anomaly with the short LAD originating from the left sinus of valsalva and the long LAD originating from the right sinus of valsalva. Identifying anatomy of the coronary artery is important when making a strategy for PCI. In types IV-VI dual LAD, the anatomic features can be misinterpreted at coronary angiography. MDCT was useful in understanding the anomaly of dual LAD and performing PCI in the present case.
一名58岁女性因胸痛前来我院就诊。多排螺旋计算机断层扫描(MDCT)显示为V型双左前降支动脉(LAD),右冠状动脉第1段狭窄90%。检查两天后,她因反复胸痛入住我院。她被诊断为急性心肌梗死。冠状动脉造影显示第1段狭窄99%,存在双LAD。她接受了第1段裸金属支架的成功经皮冠状动脉介入治疗(PCI)。V型双LAD是一种罕见且复杂的冠状动脉异常,短LAD起源于主动脉左窦,长LAD起源于主动脉右窦。制定PCI策略时,明确冠状动脉解剖结构很重要。在IV - VI型双LAD中,冠状动脉造影时解剖特征可能被误判。MDCT有助于了解本病例中双LAD的异常情况并进行PCI。