Pheochromocytoma in a 49-year-old woman presenting with acute myocardial infarction: A case report

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作者
Hao-Yu Wu [1 ]
Yi-Wei Cao [2 ]
Tian-Jiao Gao [3 ]
Jian-Li Fu [4 ]
Lei Liang [1 ]
机构
[1] Department of Cardiology,Shaanxi Provincial People’s Hospital
[2] Department of Electrocardiology,Shaanxi Provincial People’s Hospital
[3] Department of Gastroenterology,Xi’an Children’s Hospital
[4] Ultrasonic Diagnosis Center,Shaanxi Provincial People’s Hospital
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中图分类号
R736.6 [肾上腺肿瘤];
学科分类号
100214 ;
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, a VF, 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.
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页码:3752 / 3757
页数:6
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