Pheochromocytoma in von Hippel‐Lindau Disease: Clinical Features and Comparison With Sporadic Pheochromocytoma
VHL disease-related PPGLs were often multifocal and noradrenergic, and more likely to relapse compared with sporadic PPGLs. No relationships were identified between the mutation sites and the clinical characteristics of PPGLs.
Authors
- T Y Li (ORCID: https://orcid.org/0000-0001-7363-5216)
- Shi Chen (ORCID: https://orcid.org/0000-0002-8965-1015)
- Yue Zhou (ORCID: https://orcid.org/0000-0002-2639-6934)
- Ting Zhou (ORCID: https://orcid.org/0000-0002-4685-3055)
- Yunying Cui
- Lin Lü (ORCID: https://orcid.org/0000-0003-3379-8277)
- Anli Tong (ORCID: https://orcid.org/0000-0002-1418-1012)
- Yushi Zhang (ORCID: https://orcid.org/0009-0009-4841-9971)
Institutions
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Peking Union Medical College Hospital (CN)
Publication Details
- Journal
- Clinical Endocrinology
- Published
- 2024-12-25
- DOI
- https://doi.org/10.1111/cen.15190
- Citations
- 1
- Primary Topic
- Cancer, Hypoxia, and Metabolism
- Type
- article
- Field-Weighted Citation Impact
- 0.29
Funders
- Peking Union Medical College Hospital
- National Key Research and Development Program of China