以ST段抬高型心肌梗死为表现的嗜铬细胞瘤
Phaeochromocytoma presenting with ST segment elevation myocardial infarction.
作者信息
Ahmed Mohamed A, Abdullah Abdullah Sayied, Kiernan Thomas John
机构信息
University Hospital Limerick, Dooradoyle, Ireland.
Department of Cardiology, University Hospital Limerick, Limerick, Ireland.
出版信息
BMJ Case Rep. 2016 Feb 8;2016:bcr2015214134. doi: 10.1136/bcr-2015-214134.
Abstract
Phaeochromocytoma is a rare endocrine disorder with different cardiovascular presentations. In this brief report, we discuss a case of a 59-year-old woman who presented with acute ST segment elevation myocardial infarction secondary to phaeochromocytoma. Coronary angiogram showed non-obstructive coronary artery disease.
摘要
嗜铬细胞瘤是一种罕见的内分泌疾病，有不同的心血管表现。在本简要报告中，我们讨论一例59岁女性患者，该患者因嗜铬细胞瘤继发急性ST段抬高型心肌梗死。冠状动脉造影显示非阻塞性冠状动脉疾病。
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