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Clinical Syndromes and Genetic Screening Strategies of Pheochromocytoma and Paraganglioma

27 Dec 2018

Abstract excerpt

Pheochromocytomas (PCCs) are rare neuroendocrine tumors that originate from chromaffin cells of the adrenal medulla, and paragangliomas (PGLs) are extra-adrenal pheochromocytomas. These can be mainly found in clinical syndromes including multiple endocrine neoplasia (MEN), von Hippel-Lindau (VHL) syndrome, neurofibromatosis-1 (NF-1) and familial paraganglioma (FPGL). PCCs and PGLs are thought to have the highest...

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PMID: 30613466
DOI: 10.15586/jkcvhl.2018.113

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