Congenital Bilateral Wilms Tumor: A Case Report

被引：1
|
作者：
Meng, Deguang
Chang, Xiaofeng
Ren, Qinghua
Xu, Jiatong
Wang, Huanmin [1 ]
机构：
[1] Capital Med Univ, Dept Surg Oncol, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, 56 Nanlishi Rd, Beijing 100045, Peoples R China
来源：
UROLOGY | 2021年 / 157卷
关键词：
D O I：
10.1016/j.urology.2021.08.011
中图分类号：
R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];
学科分类号：
1002 ; 100201 ;
摘要：
Compare to congenital mesoblastic nephroma in fetus, congenital wilms tumor is extremely rare. Herein we report a case of congenital bilateral solid masses on antenatal ultrasound. The mass was evaluated by ultrasonography and contrast computed tomography scan in postnatal period, and the patient was undergoing tumor enucleation separately in short period after neoadjuvant chemotherapy. The diagnosis was confirmed by histology analysis for each side, and the treatment was taken according to the International Society of Pediatric Oncology. (C) 2021 Elsevier Inc.
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收藏
页码：242 / 245
页数：4
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