S. Sellami, S. Ammar, H. Fourati, M. Zouari, Manel Weli, H. Zitouni, M. B. Dhaou, R. Mhiri
{"title":"婴幼儿非转移性横纹肌样瘤与肾母细胞瘤术前如何鉴别:1例报告并文献复习","authors":"S. Sellami, S. Ammar, H. Fourati, M. Zouari, Manel Weli, H. Zitouni, M. B. Dhaou, R. Mhiri","doi":"10.46619/JOCCR.2019.2-1041","DOIUrl":null,"url":null,"abstract":"Background: Rhabdoid tumor of the kidney is an uncommon and aggressive tumor characterized by poor outcomes. Given the rarity of this tumor, the diagnosis is still a challenge and the treatment are not well codified. Case report: A 4-month-old girl presented with abdominal mass. Clinical and radiologic explorations suggested nephroblastoma. The diagnosis of rhabdoid tumor was made post operatively based on anatomopathological findings.","PeriodicalId":73665,"journal":{"name":"Journal of clinical cases & reports","volume":"50 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"How to Distinguish Non-Metastatic Rhabdoid Tumor from Wilms Tumor in Young Infants Preoperatively: A Case Report and Literature Review\",\"authors\":\"S. Sellami, S. Ammar, H. Fourati, M. Zouari, Manel Weli, H. Zitouni, M. B. Dhaou, R. Mhiri\",\"doi\":\"10.46619/JOCCR.2019.2-1041\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Rhabdoid tumor of the kidney is an uncommon and aggressive tumor characterized by poor outcomes. Given the rarity of this tumor, the diagnosis is still a challenge and the treatment are not well codified. Case report: A 4-month-old girl presented with abdominal mass. Clinical and radiologic explorations suggested nephroblastoma. The diagnosis of rhabdoid tumor was made post operatively based on anatomopathological findings.\",\"PeriodicalId\":73665,\"journal\":{\"name\":\"Journal of clinical cases & reports\",\"volume\":\"50 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-12-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of clinical cases & reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.46619/JOCCR.2019.2-1041\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of clinical cases & reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46619/JOCCR.2019.2-1041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
How to Distinguish Non-Metastatic Rhabdoid Tumor from Wilms Tumor in Young Infants Preoperatively: A Case Report and Literature Review
Background: Rhabdoid tumor of the kidney is an uncommon and aggressive tumor characterized by poor outcomes. Given the rarity of this tumor, the diagnosis is still a challenge and the treatment are not well codified. Case report: A 4-month-old girl presented with abdominal mass. Clinical and radiologic explorations suggested nephroblastoma. The diagnosis of rhabdoid tumor was made post operatively based on anatomopathological findings.
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