嗜铬细胞瘤诱发应激性心肌病1例
Stress-induced cardiomyopathy induced by pheochromocytoma:a case report
郭琰 1向定成 1张群辉 2黎思 1黄威龙 1段天兵 1顾晓龙1
作者信息
- 1. 中国人民解放军南部战区总医院心血管内科(广州,510010)
- 2. 南华大学附属第一医院心血管内科
- 折叠
摘要
嗜铬细胞瘤可诱发多种临床表现,其中应激性心肌病是其公认但罕见的临床表现.本文报道1例57岁女性患者,因突发气促就诊,临床表现类似急性冠状动脉综合征,病情进展快速且凶险,最后确诊为嗜铬细胞瘤诱发的应激性心肌病,行外科手术治疗,预后良好.
Abstract
Pheochromocytoma can induce multiple clinical manifestations,among which stress-induced car-diomyopathy is a recognized but rare clinical manifestation of pheochromocytoma.This article reports a 57-year-old female patient who sought medical attention due to sudden shortness of breath.-The clinical manifestations were similar to acute coronary syndrome,and the condition progressed rapidly and ominously.The final diagnosis was stress-induced cardiomyopathy induced by pheochromocytoma,and surgical treatment was performed with a good prognosis.
关键词
嗜铬细胞瘤/应激性心肌病/急性冠状动脉综合征Key words
pheochromocytoma/irritability cardiomyopathy/acute coronary syndrome引用本文复制引用
基金项目
广州市科技计划(202102021267)
出版年
2024
NETL
NSTL
万方数据