Mediastinal neuroendocrine tumour presenting with ECG changes: An unusual ST-Elevation Myocardial Infarction mimic

A. Borrie, T. Pegg
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Abstract

A 63-year-old male was referred to the cardiology team with a one month history of progressive chest pain and shortness of breath. This was associated with general decline, weight loss and new heart failure. Emergency Department ECG showed ST elevation throughout the chest leads and blood tests confirmed an elevated troponin. Clinical examination revealed a precordial mass. Bedside echocardiography showed an akinetic anterior wall with infiltration from a mediastinal mass. CT scan demonstrated a large mediastinal mass invading the sternum, ribs and myocardium. Biopsy showed a high grade neuroendocrine tumour of uncertain origin. Despite the need for rapid treatment of ST-Elevation Myocardial Infarction (STEMI), due care needs to be taken to ensure accurate diagnosis.
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伴有心电图变化的纵隔神经内分泌肿瘤:一种不寻常的ST段抬高心肌梗死模拟
一名63岁的男性被转诊至心脏病学团队,他有一个月的渐进性胸痛和呼吸急促病史。这与全身衰退、体重减轻和新发性心力衰竭有关。急诊科心电图显示胸部导联ST段抬高,血液检查证实肌钙蛋白升高。临床检查显示心前区肿块。床边超声心动图显示前壁不活动,纵隔肿块浸润。CT扫描显示纵隔大肿块侵犯胸骨、肋骨和心肌。活检显示一个起源不明的高级神经内分泌肿瘤。尽管ST段抬高型心肌梗死(STEMI)需要快速治疗,但仍需采取适当的护理措施以确保准确诊断。
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