Abstract
The prevalence of secondary hypertension in young adults is approximately 30%, most of which are endocrine disorders such as primary aldosteronism, pheochromocytoma/paraganglioma (PPGL), and Cushing syndrome. Pheochromocytoma and paraganglioma (PPGL) are neuroendocrine tumors that arise from adrenal or extra-adrenal chromaffin cells, and they can occur either sporadically or hereditary. It is a necessity to establish an accurate diagnosis through careful workup to provide optimal treatment.
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