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首页> 外文期刊>The Endocrinologist >Pheochromocytoma Mimicking an Acute Coronary Syndrome A Case Report and Review of Its Cardiovascular Manifestations
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Pheochromocytoma Mimicking an Acute Coronary Syndrome A Case Report and Review of Its Cardiovascular Manifestations

机译:嗜铬细胞瘤模拟急性冠状动脉综合征一例报告及其心血管表现的回顾

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摘要

A 57-year-old woman presented with intermittent, but intensifying, central chest tightness associated with electrocardiographic changes mimicking acute coronary syndrome. Eventually, a malignant pheochromocytoma was found. Elevated plasma catecholamine levels associated with pheochromocytoma can cause myocardial injury in the absence of clinically significant atherosclerotic coronary artery disease. The cardiovascular manifestations of pheochromocytoma are diverse, making early diagnosis challenging. However, rapid recognition and diagnosis of a pheochromocytoma in this setting is important in order to initiate proper therapy and reduce associated morbidity. In the current report, the pathogenesis of cardiovascular manifestations of pheochromocytoma and management of acute coronary syndrome/myocardial infarction in the presence of pheochromocytoma are discussed.
机译:一名57岁的妇女表现出间歇性但加剧的中央胸闷,与模拟急性冠脉综合征的心电图改变有关。最终发现恶性嗜铬细胞瘤。在缺乏临床上明显的动脉粥样硬化性冠状动脉疾病的情况下,与嗜铬细胞瘤相关的血浆儿茶酚胺水平升高会引起心肌损伤。嗜铬细胞瘤的心血管表现多种多样,这使得早期诊断具有挑战性。然而,在这种情况下快速识别和诊断嗜铬细胞瘤对于启动适当的治疗并减少相关的发病率很重要。在本报告中,讨论了嗜铬细胞瘤的心血管表现的发病机制以及在嗜铬细胞瘤存在的情况下急性冠脉综合征/心肌梗塞的治疗。

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