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PHEOCHROMOCYTOMA CRISIS TREATED WITH URAPIDIL: A CASE REPORT
Miro Bakula1, Lea Tomašić2, Ivana Kokan2
1Sveti Duh University Hospital, Division of Endocrinology, Department of Internal Medicine, Zagreb, Croatia.
Pheochromocytoma crisis, a rare condition, can be triggered by beta-blockers. This case report highlights successful treatment with urapidil, emphasizing careful medication management for these rare tumors.
Area of Science:
- Endocrinology
- Cardiology
- Oncology
Background:
- Pheochromocytomas are rare neuroendocrine tumors causing diverse symptoms and potential hypertensive crises.
- Catecholamine overproduction in pheochromocytoma can lead to severe cardiovascular complications.
- Triggers for pheochromocytoma crisis are varied, necessitating careful diagnostic and management approaches.
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