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A current review of the etiology, diagnosis, and treatment of pediatric pheochromocytoma and paraganglioma.
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Abstract
Pheochromocytomas and paragangliomas (PHEO/PGL) are neuroendocrine tumors that arise from sympathetic and parasympathetic paraganglia. Diagnosed rarely during childhood, PHEO/PGL are nonetheless important clinical entities, particularly given our evolving understanding of their pathophysiology.