Rhabdoid Differentiation in Wilms Tumor

Aashita, Jaspreet Kaur, Apratim Roy Choudhury, Vikas Yadav, Pragyat Thakur
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Abstract

ABSTRACT Wilms tumor (WT) is a relatively common pediatric tumor. Depending on the stage of disease, treatment includes surgery, chemotherapy, and radiotherapy. Chemotherapy and radiotherapy can induce differentiation of tumor cells to rhabdoid morphology that can masquerade as rhabdoid tumor of the kidney. We report a rare case of WT with rhabdoid differentiation subsequent to treatment with neoadjuvant chemotherapy. Rhabdoid tumor of the kidney was initially considered a sarcomatous variant of WT, however was later classified separately due to distinct behavior. This makes it challenging to differentiate from WT with rhabdoid differentiation which is important as that would also affect the aggressiveness of treatment and prognosis.
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Wilms 肿瘤中的横纹肌样分化
摘要 Wilms 肿瘤(WT)是一种比较常见的儿童肿瘤。根据疾病的不同阶段,治疗方法包括手术、化疗和放疗。化疗和放疗可诱导肿瘤细胞分化为横纹肌瘤形态,从而伪装成肾脏横纹肌瘤。我们报告了一例罕见的新辅助化疗后出现横纹肌样分化的WT病例。肾脏横纹肌瘤最初被认为是WT的肉瘤变异型,但后来由于其独特的表现而被单独分类。这使得将横纹肌瘤分化的 WT 与横纹肌瘤区分开来具有挑战性,这一点非常重要,因为这也会影响治疗的积极性和预后。
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0.00%
发文量
27
审稿时长
11 weeks
期刊最新文献
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