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Published on: August 18, 2016
Phaeochromocytoma and acute myocardial infarction
1Department of Anaesthetics, University of Natal, Congella, South Africa.
Insights
Phaeochromocytoma rarely causes myocardial infarction. This case highlights a patient with coronary artery disease who experienced a heart attack despite alpha-blockade, underscoring complex cardiovascular risks.
Area of Science:
- Cardiology
- Endocrinology
- Oncology
Background:
- Phaeochromocytoma, a rare neuroendocrine tumor, can cause significant cardiovascular complications due to catecholamine excess.
- Myocardial infarction (MI) is an uncommon but serious complication associated with phaeochromocytoma.
Observation:
- A patient with phaeochromocytoma experienced an acute myocardial infarction despite receiving alpha adrenoceptor blockade therapy.
- Coronary artery disease was identified as a coexisting condition in the patient.
Findings:
- The patient did not meet the criteria for coronary revascularization procedures.
- Adrenalectomy, the surgical removal of the adrenal gland, was successfully performed four weeks after the myocardial infarction.
Implications:
- This case prompts discussion on the contributing factors to MI in phaeochromocytoma patients, including the potential role of beta adrenoceptor blockade.
- The optimal timing for adrenalectomy and the necessity of coronary revascularization in such complex cases require careful consideration.
Abstract:
Phaeochromocytoma is uncommonly associated with myocardial infarction. We present a patient who, despite established alpha adrenoceptor blockade, sustained an acute myocardial infarction and was found to have coronary artery disease. Indications for coronary revascularization were not met, and adrenalectomy was successfully performed four weeks later. Factors contributing to the myocardial infarction, the role of beta adrenoceptor blockade, the timing of adrenalectomy and the place of coronary revascularization are discussed.
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