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Article

Multiple endocrine neoplasia 2A with RET mutation p.Cys611Tyr: A case report.

Medicine - 4 Jun 2021

Li Yan, Tan Ya-Qin, Tang Zhi-Xiang, Liao Qing-Hui, Guo Zhong-Qiu, Lai Kang-Bao, Wang Rong, Chen Yu-Hua

Abstract excerpt

RATIONALE: Multiple endocrine neoplasia 2A (MEN2A) is a rare autosomal-dominant genetic syndrome, frequently misdiagnosed or neglected clinically, resulting in delayed therapy to patients. PATIENT CONCERNS: A 47-year-old Chinese male patient underwent laparoscopic right adrenal tumorectomy, and postoperative pathology confirmed the tumor as pheochromocytoma (PHEO). He was readmitted to the department of...

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Identifiers

PMID: 34087905
DOI: 10.1097/MD.0000000000026230
PMCID: PMC8183697

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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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