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Article

Hereditary Pheochromocytoma.

International journal of surgical pathology - 1 Aug 2014

Santos Pedro, Pimenta Tiago, Taveira-Gomes Antonio

Abstract excerpt

INTRODUCTION: Pheochromocytomas (PHEO) and paragangliomas (PGL) are rare neuroendocrine tumors with an estimated occurrence of 2 to 5 patients per million per year and an incidence of about 1 per 100 000 in the general population. These tumors may arise sporadically or be associated to various syndromes, namely multiple endocrine neoplasia type 2, neurofibromatosis type 1, Von Hippel-Lindau syndrome, and...

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Source

Identifiers

PMID: 24903423
DOI: 10.1177/1066896914537683

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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