1. Inflammatory Myofibroblastic Tumor After Treatment of Wilms Tumor in a 6-Year-Old Boy: A Case Report and Literature Review
- Author
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Wen-tao Zheng, Yun-peng Li, Weiping Zhang, Le-jian He, and Wenwen Han
- Subjects
Male ,Pathology ,medicine.medical_specialty ,Urology ,030232 urology & nephrology ,Wilms Tumor ,Granuloma, Plasma Cell ,03 medical and health sciences ,Postoperative Complications ,0302 clinical medicine ,Humans ,Medicine ,cardiovascular diseases ,Child ,Confusion ,Ileal Diseases ,business.industry ,Wilms' tumor ,musculoskeletal system ,medicine.disease ,Kidney Neoplasms ,Rare tumor ,030220 oncology & carcinogenesis ,cardiovascular system ,medicine.symptom ,business ,tissues ,After treatment - 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 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.
- Published
- 2021
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