儿童患 Wilms 瘤治疗后发生炎性肌纤维母细胞瘤：病例报告及文献复习。
Inflammatory Myofibroblastic Tumor After Treatment of Wilms Tumor in a 6-Year-Old Boy: A Case Report and Literature Review.
机构信息
Department of Urology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Department of Pathology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
出版信息
Urology. 2021 Mar;149:e25-e28. doi: 10.1016/j.urology.2020.11.012. Epub 2020 Nov 19.
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.
炎性肌纤维母细胞瘤（IMT）是一种罕见的具有惰性病程的肿瘤。它作为儿科患者恶性肿瘤治疗后的第二肿瘤报道较少。在此，我们报告一例 Wilms 瘤（WT）后的 IMT，并对 IMT 和 WT 进行文献复习，以评估 IMT 作为第二肿瘤的诊断可能性。这两种肿瘤的共存可能会导致混淆，即它们是否具有遗传联系，或者 IMT 是否可能是 WT 治疗的晚期效应。
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