Published online Feb 6, 2021. doi: 10.12998/wjcc.v9.i4.951
Peer-review started: October 22, 2020
First decision: November 20, 2020
Revised: November 25, 2020
Accepted: December 11, 2020
Article in press: December 11, 2020
Published online: February 6, 2021
Processing time: 94 Days and 23 Hours
Pheochromocytoma is a rare catecholamines-secreting tumor arising from chromaffin cells in the adrenal medulla. It classically presents with paroxysmal hypertension, headaches, palpitations, sweating, and metabolic disorders. Atypical presentations such as acute myocardial infarction, heart failure, cardiomyopathy, stroke, and transient erythrocytosis have been infrequently documented.
We describe the case of a 72-year-old man diagnosed with pheochromocytoma presenting with non-ST segment elevation myocardial infarction, heart failure, and transient erythrocytosis with nonobstructed coronary arteries. This was his second heart attack. The patient was previously diagnosed with myocardial infarction, and an immense mass was found on the left adrenal gland 3 years prior. Based on clinical and laboratory findings, a diagnosis of pheochromocytoma was confirmed. His coronary angiogram showed nonobstructed coronary arteries except for a myocardial bridge in the left anterior descending branch. This was a form of type-2 myocardial infarction. The myocardial cell lesions were caused by sudden secretion of catecholamines by the pheochromocytoma. Even more atypically, his hemoglobin level was obviously elevated at admission, but after a few days of treatment with an alpha-adrenergic receptor blocker, it dropped to normal levels without additional treatment.
Pheochromocytoma may be a cause of acute myocardial infarction, heart failure, and transient erythrocytosis.
Core Tip: Pheochromocytomas release massive amounts of catecholamines that can cause life-threatening cardiovascular complications, including cardiac arrhythmia, ST and non-ST segment elevation myocardial infarction, heart failure, and hypertensive urgency. For acute myocardial infarction with unexplained erratic blood pressure, headaches, palpitations, and sweating, pheochromocytoma should be considered a differential diagnosis. Pheochromocytoma is a non-atherosclerotic cause of myocardial infarction. The myocardial cell lesions may be caused by tachycardia, coronary artery spasm, or cardiomyopathy, which are related to excess catecholamines. Pheochromocy-toma with erythrocytosis is rarely reported. Elevated hematocrit contributes to increased blood viscosity and thus, to higher risk of coronary heart disease.