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Published on: May 17, 2024
Pheochromocytoma underlying hypertension, stroke, and dilated cardiomyopathy
Pi Chi Lin1, Jen Te Hsu, Chang Min Chung
1Division of Cardiology, Chia-yi Chang Gung Memorial Hospital, Pu-TZ City, Chai Yi Hsien 613, Taiwan, Republic of China.
Insights
Pheochromocytoma, a rare adrenal tumor, can cause severe hypertension, dilated cardiomyopathy, and cerebrovascular events. Surgical removal of this tumor effectively treated the patient's symptoms and improved heart function.
Area of Science:
- Cardiology
- Endocrinology
- Neurology
Background:
- Hypertension is a common condition, but intractable cases warrant further investigation.
- Dilated cardiomyopathy and cerebrovascular events can have various underlying causes.
- Pheochromocytoma is a rare neuroendocrine tumor of the adrenal medulla.
Observation:
- A 65-year-old man with a history of hypertension presented with symptoms including dilated cardiomyopathy, a transient cerebrovascular event, and intractable hypertension.
- Diagnostic workup, including echocardiography and CT scan, was initiated due to severe sweating and hypertension.
- Coronary angiography showed no abnormalities, prompting further investigation into the cause of the patient's complex symptoms.
Findings:
- Computed tomography revealed a left adrenal pheochromocytoma.
- Surgical resection of the pheochromocytoma led to rapid resolution of hypertension.
- Cardiac function significantly improved four months post-surgery, with resolved 4-chamber dilatation and improved contractility.
Implications:
- Pheochromocytoma should be considered in the differential diagnosis for patients presenting with unexplained dilated cardiomyopathy and cerebrovascular events.
- Early diagnosis and surgical management of pheochromocytoma can reverse severe cardiovascular complications.
- This case highlights the critical link between endocrine disorders and cardiovascular/neurological manifestations.
Abstract:
We report the case of a 65-year-old man with a 6-year history of hypertension who presented with dilated cardiomyopathy, a transient cerebrovascular event, paroxysmal sweating, and intractable hypertension. Coronary angiography revealed no abnormality, but diagnostic testing was pursued because of the severe sweating and hypertension. Two-dimensional echocardiography showed 4-chamber dilatation with decreased left ventricular contractility. Further investigation, including a computed tomographic scan of the abdomen, led to a diagnosis of pheochromocytoma. Surgical resection of a left adrenal pheochromocytoma quickly resolved the patient's hypertension and resulted in substantially improved cardiac function after 4 months. Although pheochromocytoma has rarely been reported in the presence of both dilated cardiomyopathy and cerebrovascular events, it should be included in the differential diagnosis when patients present with dilated cardiomyopathy and a cerebrovascular event that have no obvious cause.
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