Familial bilateral pheochromocytoma: a case report
10.3760/cma.j.cn112330-20210909-00480
- VernacularTitle:家族性双侧嗜铬细胞瘤1例报告
- Author:
Qian HOU
1
;
Biao ZHANG
;
Panfeng SHANG
;
Ningqiang YANG
;
Yao LUO
;
Shujun YANG
;
Tianci DU
;
Pengyuan WANG
;
Chuang LUO
Author Information
1. 兰州大学第二医院泌尿外科，兰州 730030
- Keywords:
Adrenal gland;
Pheochromocytoma;
Familial;
Gene detection
- From:
Chinese Journal of Urology
2023;44(1):64-65
- CountryChina
- Language:Chinese
-
Abstract:
Familial pheochromocytoma belongs to autosomal dominant inheritance, and has complex and variable clinical manifestations. A child with bilateral PHEO was admitted to our hospital. His grandmother, father and brother were all diagnosed with PHEO, and his aunt was diagnosed with paraganglioma. The child underwent laparoscopic left partial adrenalectomy and open surgery for the contralateral tumor, and was in good postoperative condition. The blood pressure returned to normal and there was no local recurrence and metastasis during the follow-up of 8 months after the second operation.
