Phaeochromocytoma presenting as an acute coronary syndrome

Towhid Imam1, Philip Finny1,2, Alan Choo-Kang3

  • 1Basildon University Hospital, Basildon, UK.

BMJ Case Reports
|November 1, 2016
PubMed

Insights

A patient with cardiogenic shock and diabetes was diagnosed with a rare adrenal tumor, phaeochromocytoma. Surgical removal led to full recovery, highlighting the importance of considering rare diagnoses for unusual symptoms.

Area of Science:

  • Endocrinology
  • Cardiology
  • Oncology

Background:

  • A 44-year-old male with type 2 diabetes, migraine, and anxiety presented with acute cardiogenic shock and pulmonary edema.
  • He had recently undergone colonoscopy for colitis and was prescribed prednisolone.

Observation:

  • During hospitalization for myocardial infarction, the patient developed abdominal pain.
  • A CT scan revealed a large right adrenal mass, and elevated plasma-free metadrenaline levels were detected.

Findings:

  • The patient was diagnosed with phaeochromocytoma, a rare adrenal tumor.
  • A right adrenalectomy was successfully performed after 4 months.

Implications:

  • Successful surgical management normalized cardiac function and resolved diabetes in the patient.
  • Delayed diagnosis of phaeochromocytoma due to misattribution of symptoms underscores the need for comprehensive diagnostic evaluation.
  • Phaeochromocytoma can present atypically, including with acute coronary syndromes, necessitating awareness among clinicians.

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