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Thyrotoxic and pheochromocytoma multisystem crisis: a case report
Kodai Suzuki1, Takahito Miyake1, Hideshi Okada2
1Department of Emergency and Disaster Medicine, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, 501-1194, Japan.
Journal of Medical Case Reports
|June 24, 2017
Summary
This case report details a rare simultaneous occurrence of thyrotoxic crisis and pheochromocytoma multisystem crisis. Intensive cardiovascular management was crucial for stabilizing the patient
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Emergency Medicine
Background:
- Thyrotoxic crisis and pheochromocytoma multisystem crisis are rare, life-threatening endocrine emergencies.
- Simultaneous presentation of both crises is exceptionally uncommon and presents significant management challenges.
Observation:
- A 60-year-old man presented with symptoms of both thyrotoxic crisis and pheochromocytoma multisystem crisis.
- Initial management included antithyroid drugs, steroids, and cardiovascular medications.
- Despite escalating treatment, the patient exhibited persistent hemodynamic instability, necessitating further diagnostic evaluation.
Findings:
- Elevated thyroid hormones and suppressed TSH confirmed thyrotoxicosis.
- Elevated serum catecholamines and an adrenal mass indicated pheochromocytoma.
- The patient required intensive cardiovascular support, including escalating alpha and beta-adrenergic blockade, to manage simultaneous crises.
Implications:
- Simultaneous thyrotoxic and pheochromocytoma crises demand complex and individualized cardiovascular management strategies.
- Beta-blockade augmentation under intensive care was necessary for thyrotoxic crisis management, diverging from typical pheochromocytoma protocols.
- This case highlights the critical need for vigilant monitoring and tailored interventions in managing rare, co-occurring endocrine emergencies.

