Standard treatments for pheochromocytoma include1,2:
- Surgical removal of the tumor
- Medications (chemotherapy) designed to kill tumor cells
- Radiotherapy: using radio waves to destroy the tumors
- Medications to control the signs and symptoms of the disease
Types of Therapies for Pheochromocytoma:
Ninety percent of patients are cured by surgery to remove benign pheochromocytoma tumors.3 Surgery for tumor removal is typically done by laparoscopy, during which a small incision is made in the abdomen.3,4 During surgery to remove the tumor, the physician will usually examine nearby organs to determine whether the pheochromocytoma has spread to other parts of the body.
Medications are prescribed to treat the clinical signs and symptoms of pheochromocytoma.
Commonly prescribed medications include the following1:
- Alpha-adrenergic blockers to lower blood pressure
- Beta blockers for controlling rapid, irregular pulse
For patients whose tumors are successfully removed, blood pressure and hormone levels usually return to expected levels over the weeks immediately following surgery.
Citations
- National Cancer Institute. (2012). Pheochromocytoma and paraganglioma treatment (PDQ). Retrieved March 7, 2012, from https://www.ncbi.nlm.nih.gov/books/NBK82944/
- Waguespack, S. G., Rich, T., Grubbs, E., Ying, A. K., Perrier, N. D., Ayala-Ramirez, M., et al. (2010). A current review of the etiology, diagnosis, and treatment of pediatric pheochromocytoma and paraganglioma. Journal of Clinical Endocrinology and Metabolism, 95(5), 2023–2037.
- National Organization for Rare Diseases (2011). Pheochromocytoma. https://rarediseases.org/rare-diseases/pheochromocytoma/
- Lentschener, C., Gaujoux, S., Tesniere, A., & Dousset, B. (2011). Point of controversy: Perioperative care of patients undergoing pheochromocytoma removal—time for a reappraisal? European Journal of Endocrinology, 165(: 365-373.
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