Masuda Mayuka, Fujimoto Wataru, Yamashita Soichiro, Takemoto Makoto, Kuroda Koji, Imanishi Junichi, Iwasaki Masamichi, Todoroki Takafumi, Okuda Masanori, Hayashi Takatoshi
Department of Cardiology, Hyogo Prefectural Awaji Medical Center, Sumoto, Japan.
Division of Cardiovascular Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
J Cardiol Cases. 2022 Oct 28;27(2):47-51. doi: 10.1016/j.jccase.2022.10.004. eCollection 2023 Feb.
Kounis syndrome is a rare disease in which coronary spasm or acute coronary syndrome is induced by type I allergy. Concurrence of allergic reaction and chest pain are important clues to establish diagnosis. We report a rare case of Kounis syndrome without obvious signs of allergy.A 52-year-old woman experienced abdominal pain followed by ventricular fibrillation (VF) storm. Ten months earlier, the patient underwent subcutaneous implantable cardioverter-defibrillator implantation based on the previous diagnosis of idiopathic VF. In both episodes, the patient was given dental treatment and administered loxoprofen before VF onset. After we performed loxoprofen provocation test, electrocardiogram revealed ST-segment elevation in leads II, III, and aVF. Moreover, the patient developed VF again. An emergency coronary angiography after recovery showed no significant findings. However, myocardial scintigraphy presented a perfusion-metabolism mismatch in the inferior wall. Furthermore, laboratory test results after provocation revealed increased histamine level. Based on these findings, we diagnosed the patient with Kounis syndrome.Kounis syndrome without typical allergic symptoms is challenging to diagnose. Therefore, suspecting the possibility of allergic reactions and detailed history taking are important, particularly when confronted with recurrent coronary spasm, acute coronary syndrome, and inexplicable cardiac arrest.
Kounis syndrome is a rare coronary disease with vasospasm or plaque rupture, induced by type I allergy. Since Kounis syndrome without typical allergic symptoms is challenging to diagnose, a high index of suspicion is necessary. Detailed history taking can provide important clues to establish diagnosis, particularly when confronted with recurrent coronary spasm, acute coronary syndrome, and inexplicable cardiac arrest.
库尼斯综合征是一种罕见疾病,其中I型过敏可诱发冠状动脉痉挛或急性冠状动脉综合征。过敏反应与胸痛同时出现是确立诊断的重要线索。我们报告一例无明显过敏迹象的库尼斯综合征罕见病例。一名52岁女性先出现腹痛,随后发生室颤风暴。10个月前,该患者基于先前特发性室颤的诊断接受了皮下植入式心律转复除颤器植入术。在这两次发作中,患者均接受了牙科治疗,并在室颤发作前服用了洛索洛芬。我们进行洛索洛芬激发试验后,心电图显示II、III和aVF导联ST段抬高。此外,患者再次发生室颤。恢复后进行的急诊冠状动脉造影未发现明显异常。然而,心肌闪烁显像显示下壁存在灌注 - 代谢不匹配。此外,激发试验后的实验室检查结果显示组胺水平升高。基于这些发现,我们诊断该患者为库尼斯综合征。无典型过敏症状的库尼斯综合征诊断具有挑战性。因此,怀疑过敏反应的可能性并详细询问病史很重要,尤其是在面对复发性冠状动脉痉挛、急性冠状动脉综合征和不明原因的心脏骤停时。
库尼斯综合征是一种由I型过敏诱发的伴有血管痉挛或斑块破裂的罕见冠状动脉疾病。由于无典型过敏症状的库尼斯综合征诊断具有挑战性,因此需要高度怀疑。详细询问病史可为确立诊断提供重要线索,尤其是在面对复发性冠状动脉痉挛、急性冠状动脉综合征和不明原因的心脏骤停时。