Management and Long-Term Monitoring of a Young Patient with Pheochromocytoma and RET Mutation: A Case Report
Patients with MEN2A require comprehensive, long-term follow-up to monitor for recurrence of pheochromocytoma and the development of additional endocrine neoplasms. This case highlights the role of genetic testing in guiding the management of hereditary pheochromocytoma and supports the importance of personalized monitoring strategies in patients with MEN2A.
Authors
- Shufang Yang (ORCID: https://orcid.org/0000-0001-8051-9918)
- Lu Yu (ORCID: https://orcid.org/0000-0001-7842-9550)
- Qingqing Zhang (ORCID: https://orcid.org/0000-0002-4617-7384)
- Wei Xue (ORCID: https://orcid.org/0000-0001-6089-8041)
- Jing Zheng
- Yucheng Wu (ORCID: https://orcid.org/0000-0002-4895-0027)
- Bangkui Xu
Institutions
- Nantong University (CN)
- The Affiliated Taizhou People's Hospital of Nanjing Medical University (CN)
- Nanjing Medical University (CN)
Publication Details
- Journal
- International Medical Case Reports Journal
- Published
- 2025-03-01
- DOI
- https://doi.org/10.2147/imcrj.s504562
- Primary Topic
- Adrenal and Paraganglionic Tumors
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Nanjing Medical University