Inflammatory Myofibroblastic Tumor After Treatment of Wilms Tumor in a 6-Year-Old Boy: A Case Report and Literature Review

被引：4
作者：
Li, Yun-peng [1 ]
Han, Wen-wen [1 ]
He, Le-jian [2 ]
Zheng, Wen-tao [2 ]
Zhang, Wei-ping [1 ]
机构：
[1] Capital Med Univ, Beijing Childrens Hosp, Dept Urol, Natl Ctr Childrens Hlth, 56 Nanlishi St, Beijing 100045, Peoples R China
[2] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Pathol, Beijing, Peoples R China
来源：
UROLOGY | 2021年 / 149卷
关键词：
PSEUDOTUMOR;
D O I：
10.1016/j.urology.2020.11.012
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：
Inflammatory myofibroblastic tumor (IMT) is a rare tumor with an indolent course. It is less often reported as a second tumor that occurs after treatment of malignant tumors in pediatric patients. Here, we report a case of IMT following Wilms tumor (WT), and conduct a literature review concerning IMTs and WT to evaluate the diagnostic possibility of IMT as a second tumor. The coexistence of the 2 tumors may cause confusion as to whether they share genetic links or that IMTs may appear as late effects of the treatment of WT. (C) 2020 Elsevier Inc.
引用
收藏
页码：E25 / E28
页数：4
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