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表现为急性冠状动脉综合征假象的嗜铬细胞瘤。

Pheochromocytoma presenting as a mimic of acute coronary syndrome.

作者信息

Hakim Yasmin, Forbes Anna, Khan Momina, Whitelaw Benjamin C

机构信息

King's College Hospital, Denmark Hill, London.

出版信息

Acute Med. 2016;15(3):145-148.

Abstract

Chest pain with elevated serum troponin is a common clinical presentation and is normally managed as suspected myocardial infarction or acute coronary syndrome (ACS). We report a 49 year old man who presented with central chest pain sweating and breathlessness. He had a significantly elevated serum troponin I level and a subsequent angiogram showed near normal coronary arteries. He was subsequently investigated for fever and found to have a 3cm right sided adrenal mass consistent with a pheochromocytoma. After confirmation and appropriate blockade laparoscopic adrenalectomy was performed. Pheochromocytoma may present as a mimic of acute coronary syndrome but this is often unrecognized and leaves the patient at risk of future pheo crisis events which may be fatal.

摘要

血清肌钙蛋白升高伴胸痛是一种常见的临床表现,通常按疑似心肌梗死或急性冠状动脉综合征(ACS)进行处理。我们报告一名49岁男性,他出现中央胸痛、出汗和呼吸急促。他的血清肌钙蛋白I水平显著升高,随后的血管造影显示冠状动脉近乎正常。随后他因发热接受检查,发现右侧肾上腺有一个3cm的肿块,符合嗜铬细胞瘤。确诊并进行适当阻断后,实施了腹腔镜肾上腺切除术。嗜铬细胞瘤可能表现为急性冠状动脉综合征的假象,但这往往未被识别,使患者面临未来可能致命的嗜铬细胞瘤危象事件的风险。

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