Hereditary pheochromocytoma with the von Hippel-Lindau gene mutation in a child: A case report

Asian J Surg. 2023 May;46(5):2256-2258. doi: 10.1016/j.asjsur.2022.11.129. Epub 2022 Dec 15.

Authors

Shengqi Zheng¹, Guicao Yin¹, Ming Zhou¹, Yifan Li²

Affiliations

¹ Department of Urology, The Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, 225000, Jiangsu Province, China.
² Department of Urology, The Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, 225000, Jiangsu Province, China. Electronic address: yfli@bjmu.edu.cn.

PMID: 36528531
DOI: 10.1016/j.asjsur.2022.11.129

No abstract available

Keywords: Child; Pheochromocytoma; Von Hippel-Lindau disease.

Publication types

Case Reports
Letter

MeSH terms

Adrenal Gland Neoplasms* / diagnostic imaging
Adrenal Gland Neoplasms* / genetics
Adrenal Gland Neoplasms* / surgery
Child
Humans
Mutation
Pheochromocytoma* / genetics
Pheochromocytoma* / surgery