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.

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