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

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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… Click to show full abstract

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 co-existence of the two tumors may cause confusion as to whether they share genetic links or that IMTs may appear as late effects of the treatment of WT.

Keywords: tumor; myofibroblastic tumor; literature review; treatment; wilms tumor; inflammatory myofibroblastic

Journal Title: Urology
Year Published: 2020

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