Takotsubo syndrome associated with coronary microvascular dysfunction: A case study

Q4 Medicine
Shohei Ikeda MD, PhD, Morihiko Takeda MD, PhD, Koichi Sato MD, PhD, Mariko Shinozaki MD, Satomi Watanabe MD, Keita Miki MD, PhD, Michinori Hirano MD, PhD, Koji Fukuda MD, PhD, FJCC, Nobuyuki Shiba MD, PhD
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Abstract

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.

Learning objective

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.

伴有冠状动脉微血管功能障碍的塔克次氏综合征:病例研究
患者是一名 68 岁的男性,因胸痛到我院急诊室就诊,由于心肌肌钙蛋白-I 水平升高,急诊心导管检查被要求进行。虽然没有发现明显的冠状动脉狭窄,但左心室有心尖气囊壁运动的证据,因此被诊断为塔库洼综合征。三个月后,他偶尔会在休息时感到胸痛,这促使我们再次对他进行心导管检查。左心室造影显示收缩正常。突然,他感到胸痛并伴有 ST 段抬高,而且是自发的。随后,我们在左前降支动脉(LAD)中间部分观察到慢流现象。我们及时注射了硝酸甘油以缓解症状。在确诊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,但仍无症状。一年后,我们再次进行了心导管检查,以进一步了解他的病情。进行了乙酰胆碱激发试验,结果显示心外膜冠状动脉没有痉挛。但在冠状窦血液样本中观察到乳酸升高。此外,LAD 的冠状动脉生理测量显示微循环阻力指数较高,冠状动脉血流储备较低。学习目的冠状动脉微血管功能障碍(CMD)被越来越多的人认为是一种重要的心血管疾病,它可导致心肌缺血,偶尔还与塔克次氏综合征(TTS)有关。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,突出了识别 TTS 患者 CMD 的重要性。
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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来源期刊
Journal of Cardiology Cases
Journal of Cardiology Cases Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.90
自引率
0.00%
发文量
177
审稿时长
59 days
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