{"title":"成人肾母细胞瘤:罕见病例报告，在转移性疾病中有特殊的生存","authors":"Kabre Rs, Kamble Km","doi":"10.5530/OGH.2017.6.1.8","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"4 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Adult Wilms Tumour: Rare case report with an exceptional survival in metastatic disease\",\"authors\":\"Kabre Rs, Kamble Km\",\"doi\":\"10.5530/OGH.2017.6.1.8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":166206,\"journal\":{\"name\":\"Oncology, Gastroenterology and Hepatology Reports\",\"volume\":\"4 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oncology, Gastroenterology and Hepatology Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5530/OGH.2017.6.1.8\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oncology, Gastroenterology and Hepatology Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5530/OGH.2017.6.1.8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Adult Wilms Tumour: Rare case report with an exceptional survival in metastatic disease
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.
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