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Published on: September 15, 2017
Cardiovascular manifestations of phaeochromocytoma
Aleksander Prejbisz1, Jacques W M Lenders, Graeme Eisenhofer
1Department of Hypertension, Institute of Cardiology, Warsaw, Poland. ajanu@op.pl
Insights
Phaeochromocytoma, a rare tumor, can cause severe cardiovascular issues like hypertension and arrhythmias due to excess catecholamines. Early screening is vital for patients with symptoms suggesting this condition.
Area of Science:
- Endocrinology
- Cardiology
- Oncology
Background:
- Phaeochromocytoma is a neuroendocrine tumor that secretes catecholamines.
- Cardiovascular manifestations are common and can be life-threatening.
Purpose of the Study:
- To review the cardiovascular manifestations of phaeochromocytoma.
- To update on the cause, clinical presentation, and treatment.
Main Methods:
- Literature review of phaeochromocytoma and its cardiovascular effects.
- Analysis of clinical presentations and outcomes.
Main Results:
- Hypertension and arrhythmias are prevalent.
- Cardiomyopathy, including Takotsubo, is a recognized complication.
- Rarely presents with hypotension or shock.
Conclusions:
- Cardiovascular complications of phaeochromocytoma can be severe.
- Screening is recommended for patients with suggestive symptoms of catecholamine excess.
Abstract:
Clinical expression of phaeochromocytoma may involve numerous cardiovascular manifestations, but usually presents as sustained or paroxysmal hypertension associated with other signs and symptoms of catecholamine excess. Most of the life-threatening cardiovascular manifestations of phaeochromocytoma, such as hypertensive emergencies, result from a rapid and massive release of catecholamines from the tumour. More rarely, patients with phaeochromocytoma present with low blood pressure or even shock that may then precede multisystem crisis. Sinus tachycardia, with palpitations as the presenting symptom, is the most prevalent abnormality of cardiac rhythm in phaeochromocytoma, but tumours can also be associated with more serious ventricular arrhythmias or conduction disturbances. Reversible dilated or hypertrophic cardiomyopathy are well established cardiac manifestations of phaeochromocytoma, with more recent attention to an increasing number of cases with Takotsubo cardiomyopathy. This review provides an update on the cause, clinical presentation and treatment of the cardiovascular manifestations of phaeochromocytoma. As the cardiovascular complications of phaeochromocytoma can be life-threatening, all patients who present with manifestations that even remotely suggest excessive catecholamine secretion should be screened for the disease.
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