Pheochromocytoma and Paraganglioma—Patient Version
Pheochromocytoma and paraganglioma are rare tumors that can be benign (not cancer) or malignant. Pheochromocytomas form in the adrenal glands, and paragangliomas usually along nerve pathways in the head, neck, and spine. Explore the links on this page to learn more about these tumors, their treatment, research, and clinical trials.
Patient Information Related to Pheochromocytoma and Paraganglioma
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Pheochromocytoma and Paraganglioma Treatment
Pheochromocytoma and paraganglioma treatment is usually surgery and drug therapy. Chemotherapy, radiation, targeted therapy, ablation, and embolization are options for disease that has spread or returned. Learn more in this expert-reviewed summary.
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Childhood Pheochromocytoma & Paraganglioma Treatment
Childhood pheochromocytoma and paraganglioma treatment options include surgery, chemotherapy, high-dose 131I-MIBG therapy, and targeted therapy. Learn more about risk factors, symptoms, diagnosis, and treatment in this expert-reviewed summary.
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Clinical Trials for Pheochromocytoma
Find a list of pheochromocytoma clinical trials and use filters to refine the results.
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Clinical Trials for Paraganglioma
Find a list of paraganglioma clinical trials and use filters to refine the results.