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Article

Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a case.

Surgery today - 1 Nov 2014

Hibi Yatsuka, Ohye Tamae, Ogawa Kimio, Shimizu Yoshimi, Shibata Masahiro, Kagawa Chikara, Mizuno Yutaka, Uchino Shinya, Kosugi Shinji, Kurahashi Hiroki, Iwase Katsumi

Abstract excerpt

We report a rare case with pheochromocytoma as the first manifestation of multiple endocrine neoplasia type 2A with RET mutation S891A. Bilateral pheochromocytomas were identified in a 54-year-old woman. Screening for RET revealed a rare S891A mutation located in the intracellular tyrosine kinase domain. This mutation was previously recognized as one of the mutations only in cases manifesting solely medullary...

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Identifiers

PMID: 24449023
DOI: 10.1007/s00595-013-0826-8
PMCID: PMC4194010

Genes

RET

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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