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Article

The characterization of pheochromocytoma and its impact on overall survival in multiple endocrine neoplasia type 2.

The Journal of clinical endocrinology and metabolism - 1 Nov 2013

Thosani Sonali, Ayala-Ramirez Montserrat, Palmer Lynn, Hu Mimi I, Rich Thereasa, Gagel Robert F, Cote Gilbert, Waguespack Steven G, Habra Mouhammed Amir, Jimenez Camilo

Abstract excerpt

CONTEXT: Pheochromocytoma (PHEO) occurs in 50% of patients with multiple endocrine neoplasia type 2 (MEN2). It is unknown if the presence of PHEO is associated with more aggressive medullary thyroid cancer (MTC). OBJECTIVE: To present our experience with MEN2 PHEO and evaluate whether PHEO impacts MTC overall survival in patients with RET codon 634 mutations. DESIGN: We performed a retrospective chart review of...

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Source

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Identifiers

PMID: 24030942
DOI: 10.1210/jc.2013-1653
PMCID: PMC5399523

Genes

RET

Provenance

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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