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Adult Wilms Tumour: Rare case report with an exceptional survival in metastatic disease

机译:成年威尔姆氏瘤:罕见病例报告,转移性疾病存活率高

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Incidence of wilms tumour(WT) in adults is low, the exact number is unknown owing to insufficient documentation or incorrect diagnosis. Compared to their paediatric counterparts, adult wilms tumour has shown poorer prognosis, but with use of multi-modality treatment there is improvement in response and overall survival. Here in this case report we discuss a case of adult wilms tumour with characteristic triphasic histology & unusual 3 year survival post operatively with irregular treatment in the face of metastatic disease.
机译:成人的野生肿瘤(WT)发病率低,由于文献不足或诊断错误,确切的数目尚不清楚。与小儿同行相比,成年Wilm肿瘤预后较差,但采用多模式治疗可改善反应和总体生存率。在本病例报告中,我们讨论了一例具有特征性三层组织学特征且在手术后面对转移性疾病不规则治疗的3年生存率异常的成人蠕虫肿瘤。

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