Ikeda Shohei, Takeda Morihiko, Sato Koichi, Shinozaki Mariko, Watanabe Satomi, Miki Keita, Hirano Michinori, Fukuda Koji, Shiba Nobuyuki
Department of Cardiology, International University of Health and Welfare Hospital, Tochigi, Japan.
J Cardiol Cases. 2023 Dec 7;29(3):124-127. doi: 10.1016/j.jccase.2023.11.005. eCollection 2024 Mar.
The patient, a 68-year-old man, presented to our emergency room with chest pain, prompting an emergency cardiac catheterization due to elevated cardiac troponin-I levels. While no obvious coronary artery stenosis was found, there was evidence of apical ballooning wall motion in the left ventricle, leading to a diagnosis of takotsubo syndrome. Three months later, he occasionally experienced chest pain at rest, prompting us to conduct another cardiac catheterization. Left ventriculography showed normal contraction. Suddenly, he experienced chest pain accompanied by ST elevation, which occurred spontaneously. Subsequently, slow-flow phenomenon was observed in the intermediate part of left anterior descending artery (LAD). We promptly administered nitroglycerin to alleviate the symptoms. Following the diagnosis of coronary microvascular dysfunction (CMD), he started calcium-channel blocker therapy and remained asymptomatic. One year later, we re-performed cardiac catheterization to further explore his condition. Acetylcholine provocation test was performed, which showed no epicardial coronary spasm. However, lactic acid elevation was observed in the coronary sinus blood sample. Additionally, a coronary physiological measurement in the LAD revealed a high index of microcirculatory resistance and low coronary flow reserve. Based on this series of clinical events, we inferred a significant contribution of CMD to the patient's condition.
Coronary microvascular dysfunction (CMD) is increasingly recognized as an important cardiovascular disease, leading to myocardial ischemia, which is occasionally associated with takotsubo syndrome (TTS). In this report, we present a case of spontaneous CMD associated with TTS. This case emphasizes the significance of accurate diagnosis and appropriate treatment, highlighting the importance of recognizing CMD in patients with TTS.
该患者为一名68岁男性,因胸痛就诊于我院急诊室,由于心肌肌钙蛋白I水平升高而接受了紧急心脏导管插入术。虽然未发现明显的冠状动脉狭窄,但有左心室心尖部气球样壁运动的证据,从而诊断为应激性心肌病。三个月后,他偶尔在静息时出现胸痛,促使我们再次进行心脏导管插入术。左心室造影显示收缩正常。突然,他出现胸痛并伴有ST段抬高,疼痛自发出现。随后,在左前降支(LAD)中段观察到血流缓慢现象。我们立即给予硝酸甘油以缓解症状。在诊断为冠状动脉微血管功能障碍(CMD)后,他开始接受钙通道阻滞剂治疗,此后一直无症状。一年后,我们再次进行心脏导管插入术以进一步探究他的病情。进行了乙酰胆碱激发试验,结果显示无冠状动脉痉挛。然而,在冠状窦血样中观察到乳酸升高。此外,对LAD进行的冠状动脉生理测量显示微循环阻力指数高且冠状动脉血流储备低。基于这一系列临床事件,我们推断CMD对该患者的病情有重大影响。
冠状动脉微血管功能障碍(CMD)越来越被认为是一种重要的心血管疾病,可导致心肌缺血,偶尔与应激性心肌病(TTS)相关。在本报告中,我们介绍了一例与TTS相关的自发性CMD病例。该病例强调了准确诊断和适当治疗的重要性,突出了在TTS患者中认识CMD的重要性。