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作 者:Hao-Yu Wu Yi-Wei Cao Tian-Jiao Gao Jian-Li Fu Lei Liang
机构地区:[1]Department of Cardiology,Shaanxi Provincial People’s Hospital,Xi'an 710068,Shaanxi Province,China [2]Department of Electrocardiology,Shaanxi Provincial People’s Hospital,Xi'an 710068,Shaanxi Province,China [3]Department of Gastroenterology,Xi’an Children’s Hospital,Xi'an 710068,Shaanxi Province,China [4]Ultrasonic Diagnosis Center,Shaanxi Provincial People’s Hospital,Xi’an 710068,Shaanxi Province,China
出 处:《World Journal of Clinical Cases》2021年第15期3752-3757,共6页世界临床病例杂志
基 金:the Natural Science Basic Research Program of Shaanxi Province,No.2020JQ-939;and the Science and Technology Development Incubation Fund Project of Shaanxi Provincial People’s Hospital,No.2019YXQ-08.
摘 要:BACKGROUND Pheochromocytoma is a rare endocrine tumor arising from chromaffin cells and having extensive and profound effects on the cardiovascular system by continuously or intermittently releasing catecholamines.The clinical manifestations of pheochromocytoma are diverse,and the typical triad,including episodic headache,palpitations,and sweating,only occurs in 24%of pheochromocytoma patients,which often misleads clinicians into making an incorrect diagnosis.We herein report the case of a patient with intermittent chest pain and elevated myocardial enzymes for 2 years who was diagnosed with pheochromocytoma.CASE SUMMARY A 49-year-old woman presented with intermittent chest pain for 2 years.Two years ago,the patient experienced chest pain and was diagnosed with acute myocardial infarction,with 25%stenosis in the left circumflex.The patient still had intermittent chest pain after discharge.Two hours before admission to our hospital,the patient experienced chest pain with nausea and vomiting,lasting for 20 min.Troponin I and urinary norepinephrine and catecholamine levels were elevated.An electrocardiogram indicated QT prolongation and ST-segment depression in leads II,III,aVF,and V3-V6.A coronary computed tomography angiogram revealed no evidence of coronary artery disease.Echocardiography showed left ventricular enlargement and a decreased posterior inferior wall motion amplitude.Contrast-enhanced computed tomography demonstrated an inhomogeneous right adrenal mass.The patient successfully underwent laparoscopic right adrenalectomy,and histopathology confirmed adrenal pheochromocytoma.During the first-year follow-up visits,the patient was asymptomatic.The abnormal changes on echocardiography and electro-cardiogram disappeared.CONCLUSION Clinicians should be aware of pheochromocytoma.A timely and accurate diagnosis of pheochromocytoma is essential for alleviating serious cardiac complications.
关 键 词:PHEOCHROMOCYTOMA CATECHOLAMINE Cardiac complications Acute myocardial infarction Chest pain Case report
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