Yamamoto Hiroyuki, Otake Hiromasa, Tanimura Kosuke, Hirata Ken-Ichi
Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 6500017, Japan.
Division of Cardiovascular Medicine, Hyogo Brain and Heart Center, Himeji 670-0981, Japan.
Eur Heart J Case Rep. 2022 May 4;6(5):ytac178. doi: 10.1093/ehjcr/ytac178. eCollection 2022 May.
Kounis syndrome (KS) is an acute coronary syndrome (ACS) induced by allergic reactions. Currently, there are three variants of KS based on the mechanism and onset of ACS. We report a rare case of KS, wherein ACS was caused by all KS variants.
A 68-year-old man with a history of percutaneous coronary intervention (PCI) for ST-segment elevation myocardial infarction of the left anterior descending artery 16 days ago underwent a staged PCI for the mid-left circumflex artery (LCx) stenosis under optical coherence tomography (OCT) guidance using low-molecular-weight dextran (LMWD). During OCT examination, the LMWD induced an anaphylactic reaction. The patient was immediately administered medications to manage the anaphylaxis; however, he complained of chest discomfort. Coronary angiography and subsequent intravascular ultrasound revealed a newly developed coronary thrombus in the proximal LCx. Furthermore, coronary spasm or multiple stent thromboses occurred sequentially in all coronary arteries, resulting in triple-vessel coronary artery ischaemia. Balloon angioplasty was performed under intra-aortic balloon pumping, which could rescue the patient. The patient was discharged without any complications 11 days post-KS, under a 7-day anti-histamine regimen. No further cardiovascular events had occurred by 1-year follow-up.
This case documented the clinical course of KS caused by LMWD, wherein all KS variants occurred sequentially. Early recognition of KS and appropriate management with anaphylaxis medication and balloon angioplasty under mechanical circulatory support effectively prevent vascular morbidity. Interventionalists should be aware of this rare and serious complication of PCI.
库尼斯综合征(KS)是一种由过敏反应诱发的急性冠状动脉综合征(ACS)。目前,根据ACS的机制和发病情况,KS有三种变体。我们报告一例罕见的KS病例,其中ACS由所有KS变体引起。
一名68岁男性,16天前因左前降支ST段抬高型心肌梗死接受经皮冠状动脉介入治疗(PCI),此次在光学相干断层扫描(OCT)引导下,使用低分子右旋糖酐(LMWD)对左回旋支(LCx)中段狭窄进行分期PCI。在OCT检查期间,LMWD引发过敏反应。患者立即接受药物治疗以控制过敏反应;然而,他仍诉说胸部不适。冠状动脉造影及随后的血管内超声检查显示,LCx近端新出现冠状动脉血栓。此外,所有冠状动脉依次发生冠状动脉痉挛或多处支架血栓形成,导致三支冠状动脉缺血。在主动脉内球囊反搏支持下进行球囊血管成形术,成功挽救了患者。KS发作11天后,患者在接受7天抗组胺治疗方案后出院,无任何并发症。随访1年,未发生进一步的心血管事件。
本病例记录了由LMWD引起的KS的临床过程,其中所有KS变体依次出现。早期识别KS并在机械循环支持下使用抗过敏药物和球囊血管成形术进行适当处理,可有效预防血管并发症。介入医生应意识到PCI的这种罕见且严重的并发症。