You’ll most likely need surgery to remove the tumor. The clinical syndrome of severe and symptomatic paroxysmal hypertension always generates suspicion of a catecholamine-secreting pheochromocytoma. Chemotherapy, radiation or radionuclide therapy are also treatment options in some cases. Treatment of pheochromocytoma in adults. 37 Full PDFs related to this paper. ↑WJ Elliott, J Varon. pheochromocytoma is the hypertensive crisis due to the tumoral secretion of catecholamines (1). Briggs et al. But tumors can develop in both. If a pheochromocytoma isn't treated, severe or life-threatening damage to other body systems can … Pheochromocytoma. Amlodipine (Norvasc) is given in a dose from 10–20 mg, and nicardipine (Cardene) in a … Although labetalol has been used in the pharmacological treatment of pheochromocytoma [Van Stratum et al., 1983] [Yabe et al., 1987], its use is controversial [Reach et al., 1980]. Learn more in this expert-reviewed summary. Malignant pheochromocytoma: effective treatment with a combination of cyclophosphamide, vincristine, and dacarbazine Ann Intern Med. Treatment of pheochromocytoma in adults. Usually, a pheochromocytoma develops in only one adrenal gland. When a tumor composed of the same cells as a pheochromocytoma develops outside the adrenal gland, it is referred to as a paraganglioma. In: UpToDate, Post TW (Ed), UpToDate, Waltham, MA. Download PDF. Treatment of pheochromocytoma … P. Saenz Rico Cruz. Your doctor may be able to do this using tiny cuts instead of one large opening. Pheochromocytoma Treatment. Authors S D Averbuch 1 , C S Steakley, R C Young, E P Gelmann, D S Goldstein, R Stull, H R Keiser. This paper. 1 However, most patients with this disorder do not have this tumor and, once it is ruled out, diagnostic investigation rarely uncovers a cause. Discussions Epidemiology and etiology Pheochromocytoma occurs with equal frequency in Drugs used for the treatment of hypertensive emergencies. The treatment of choice for the condition is to surgically remove the tumor. In some medical institutions, calcium channel blockers are the primary preoperative treatment of choice in normotensive patients with pheochromocytoma . Chemotherapy, radiation therapy, targeted therapy, ablation, and embolization can be used for disease that has spread or come back. 1988 Aug 15;109(4):267-73. doi: 10.7326/0003-4819-109-4-267. Pheochromocytoma, if detected early, can be successfully treated and managed in the vast majority of cases. Pheochromocytoma is a catecholamine-secreting tumor derived from chromaffin cells. If you have a pheochromocytoma, the tumor releases hormones that may cause high blood pressure, headache, sweating and symptoms of a panic attack. A short summary of this paper. (Accessed on January 11, 2016.) Download. ; Headache, sweating, and a fast heartbeat are typical symptoms, usually in association with markedly high blood pressure.A pheochromocytoma secretes catecholamine hormones (adrenaline and related hormones) … These neuroendocrine tumors are capable of producing and releasing massive amounts of … Surgical removal of the tumor represents the treatment of choice in order to cure and prevent cardiovascular complications (3). Pheochromocytoma is a relatively rare tumor of the adrenal glands or of similarly specialized cells outside of the adrenal glands. Pheochromocytoma and paraganglioma treatment is usually surgery and drug therapy. Download Full PDF Package. Most remain ineffectively treated, and many experience chronic disability. READ PAPER. The majority of tumors originate in the adrenal medulla, but they may also arise from sympathetic ganglia (also referred to as paraganglioma). Pheochromocytoma (PHEO or PCC) is a rare tumor of the adrenal medulla composed of chromaffin cells, also known as pheochromocytes.