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Up to: Adrenal gland neoplasm

Pheochromocytoma-paraganglioma

A rare neuroendocrine tumor arising from chromaffin cells of the adrenal medulla (pheochromocytoma) or from sympathetic and parasympathetic ganglia (paraganglioma). These tumors are most often benign and may produce catecholamines in excess causing hypertension and sometimes severe acute cardiovascular complications.

18 trials tagged with this condition →

This condition has no sub-types.