• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

PMID:27759750
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。

相似文献

1
Pheochromocytoma presenting as a mimic of acute coronary syndrome.表现为急性冠状动脉综合征假象的嗜铬细胞瘤。
Acute Med. 2016;15(3):145-148.
2
Pheochromocytoma mimicking both acute coronary syndrome and sepsis: a case report.嗜铬细胞瘤既表现为急性冠状动脉综合征又表现为脓毒症:一例报告。
Med Princ Pract. 2013;22(4):405-7. doi: 10.1159/000343578. Epub 2012 Oct 27.
3
An unusual case of pheochromocytoma mimicking both acute coronary syndrome and central nervous system infection. Case report and literature review.一例罕见的嗜铬细胞瘤病例,同时酷似急性冠状动脉综合征和中枢神经系统感染。病例报告及文献综述。
Hellenic J Cardiol. 2017 Sep-Oct;58(5):372-377. doi: 10.1016/j.hjc.2016.12.008. Epub 2017 Jan 17.
4
A case of pheochromocytoma crisis simulating acute coronary syndrome and multiple organ dysfunction syndrome.一例模拟急性冠状动脉综合征和多器官功能障碍综合征的嗜铬细胞瘤危象病例。
Hellenic J Cardiol. 2018 Nov-Dec;59(6):370-372. doi: 10.1016/j.hjc.2018.01.012. Epub 2018 Feb 13.
5
Pheochromocytoma mimicking a non-ST elevation acute myocardial infarction.酷似非ST段抬高型急性心肌梗死的嗜铬细胞瘤
Cardiol J. 2009;16(4):355-7.
6
Episodic palpitations in pheochromocytoma.嗜铬细胞瘤中的发作性心悸
CMAJ. 2009 Nov 10;181(10):714. doi: 10.1503/cmaj.090124. Epub 2009 Sep 28.
7
Malignant pheochromocytoma: pain, palpitation, perspiration and perplexities.恶性嗜铬细胞瘤:疼痛、心悸、出汗和困惑。
BMJ Case Rep. 2021 Jun 24;14(6):e239991. doi: 10.1136/bcr-2020-239991.
8
Phaeochromocytoma--"the great mimic": an unusual presentation.嗜铬细胞瘤——“伟大的伪装者”:一种不寻常的表现。
Emerg Med J. 2007 Sep;24(9):672-3. doi: 10.1136/emj.2007.049569.
9
Pheochromocytoma: a cause of ST-segment elevation myocardial infarction, transient left ventricular dysfunction, and takotsubo cardiomyopathy.嗜铬细胞瘤:ST 段抬高型心肌梗死、短暂性左心室功能障碍和心尖球形综合征的病因。
Endocr Pract. 2012 Jul-Aug;18(4):e77-80. doi: 10.4158/EP11346.CR.
10
Phaeochromocytoma presenting as an acute coronary syndrome.表现为急性冠状动脉综合征的嗜铬细胞瘤。
BMJ Case Rep. 2016 Oct 26;2016:bcr2016214737. doi: 10.1136/bcr-2016-214737.