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Introduction: Pherochromocytoma (PH) and paraganglioma (PG) are neuroendocrine tumors arising in cromaffin cells in the adrenal medulla or extra adrenal paraganglia respectively. Clinical presentation is diverse. All PG/PH have malignant potential. Hereditary cases comprise up to 40% of all PG/PH.
Conference: 17th Annual ENETSConcerence (2020)
Presenting Author:
Authors: Dioca M, Calabretta M, Iglesias L, Rojas Bilbao E, Califano I,
Keywords: Pherochromocytoma and paraganglioma (PG),
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