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Updated: Jun 4, 2025

A Novel Method: Super-selective Adrenal Venous Sampling
Published on: September 15, 2017
Metastatic Pheochromocytoma/Paraganglioma Overproducing Multiple Catecholamines.
Keiko Yoshioka1, Yujiro Nakano1, Moeka Horichi1
1Department of Endocrinology and Metabolism, Kanazawa University Graduate School of Medical Sciences, Kanazawa University, Kanazawa, 920-8641, Ishikawa, Japan.
This study presents a rare case of pheochromocytoma and paraganglioma (PPGL) with a unique dopamine secretion profile. Heterogeneity in nuclear imaging may indicate varying tumor differentiation and catecholamine output in PPGL.
Area of Science:
- Endocrinology
- Oncology
- Medical Imaging
Background:
- Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors originating from chromaffin cells.
- These tumors are characterized by the excessive production of catecholamines like adrenaline, noradrenaline, and sometimes dopamine.
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