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先天性双侧肾母细胞瘤:一例报告。

Congenital Bilateral Wilms Tumor: A Case Report.

机构信息

Baoding Children's Hospital, Baoding, Hebei, PR China.

Department of Surgical Oncology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, PR China.

出版信息

Urology. 2021 Nov;157:242-245. doi: 10.1016/j.urology.2021.08.011. Epub 2021 Aug 24.

Abstract

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.

摘要

与胎儿先天性中胚层肾瘤相比,先天性肾母细胞瘤极为罕见。本文报道了一例产前超声检查发现双侧先天性实性肿块的病例。在新生儿期,通过超声和对比增强 CT 扫描对肿块进行了评估,并在新辅助化疗后短期内分别进行了肿瘤剜除术。通过对每一侧的组织学分析进行诊断,并根据国际小儿肿瘤学会的治疗方案进行治疗。

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