{"title":"成人艾滋病毒感染者横纹肌肉瘤","authors":"S. Jhawar, G. Sharma, H. Ballard","doi":"10.12788/J.CMONC.0041","DOIUrl":null,"url":null,"abstract":"Rhabdomyosarcomas are a rare group of soft tissue neoplasms of mesenchymal origin. RMS is common among childhood cancers, but it is among the rarest of adult tumors. They account for about 5% of all childhood cancers. Soft-tissue sarcomas account for less than 1% of adult malignancies, and RMS account for only 3% of those sarcomas. Here, we report a case of RMS in the neck, which led to dysphagia due to external compression of the esophagus.","PeriodicalId":72649,"journal":{"name":"Community oncology","volume":"10 1","pages":"175-177"},"PeriodicalIF":0.0000,"publicationDate":"2013-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rhabdomyosarcoma in an adult with HIV\",\"authors\":\"S. Jhawar, G. Sharma, H. Ballard\",\"doi\":\"10.12788/J.CMONC.0041\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Rhabdomyosarcomas are a rare group of soft tissue neoplasms of mesenchymal origin. RMS is common among childhood cancers, but it is among the rarest of adult tumors. They account for about 5% of all childhood cancers. Soft-tissue sarcomas account for less than 1% of adult malignancies, and RMS account for only 3% of those sarcomas. Here, we report a case of RMS in the neck, which led to dysphagia due to external compression of the esophagus.\",\"PeriodicalId\":72649,\"journal\":{\"name\":\"Community oncology\",\"volume\":\"10 1\",\"pages\":\"175-177\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Community oncology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.12788/J.CMONC.0041\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Community oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12788/J.CMONC.0041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Rhabdomyosarcomas are a rare group of soft tissue neoplasms of mesenchymal origin. RMS is common among childhood cancers, but it is among the rarest of adult tumors. They account for about 5% of all childhood cancers. Soft-tissue sarcomas account for less than 1% of adult malignancies, and RMS account for only 3% of those sarcomas. Here, we report a case of RMS in the neck, which led to dysphagia due to external compression of the esophagus.