Wilms Tumor and a Duplex Collecting System: A Case Report and Review of Literature

被引：4

作者：

Kajbafzadeh, Abdol-Mohammad ^{[1
]}

Harsini, Sara ^{[1
]}

Baghayee, Arash ^{[1
]}

Javan-Farazmand, Niloufar ^{[1
]}

机构：

[1] Univ Tehran Med Sci, Pediat Urol Res Ctr, Dept Pediat Urol, Childrens Hosp Med Ctr, Tehran 1998714616, Iran

来源：

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 2013年 / 35卷 / 03期

关键词：

duplex collecting system; ureter; Wilms tumor; RISK; CHILDREN;

D O I：

10.1097/MPH.0b013e31826683a8

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Wilms tumor (WT) is described as a component of many different clinical conditions and genetic syndromes. However, the simultaneous occurrence of WT and a duplex collecting system is extremely rare. We report a case of a 4-year-old boy diagnosed with WT and a left duplex collecting system. The patient underwent a left radical nephrectomy. The histologic examination diagnosed it to be a case of WT with favorable histology. The patient received the chemotherapy regimen for stage 1 WT and was in complete remission during the follow-up period of 2 years. Further investigations are required for assessing the need for screening of WT in children with genitourinary malformations.

引用

页码：E109 / E111

页数：3

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