M. Sung, S. Ko, M. Hsieh, Yi Ju Chen, Wei Jen Chen, Hsuan-Ying Huang
{"title":"Thymoliposarcoma。","authors":"M. Sung, S. Ko, M. Hsieh, Yi Ju Chen, Wei Jen Chen, Hsuan-Ying Huang","doi":"10.32388/hgk9ui","DOIUrl":null,"url":null,"abstract":"Thymoliposarcoma is an exceedingly rare thymic neoplasm with only five reports in English literature to date. We report another patient, a 36-year-old male, who developed local recurrences 4-years after initial resection. The clinicopathologic features of the present and previously reports were compared with particular emphasis on their morphologic spectrum and differential diagnosis.","PeriodicalId":436929,"journal":{"name":"The Annals of thoracic surgery","volume":"28 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Thymoliposarcoma.\",\"authors\":\"M. Sung, S. Ko, M. Hsieh, Yi Ju Chen, Wei Jen Chen, Hsuan-Ying Huang\",\"doi\":\"10.32388/hgk9ui\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Thymoliposarcoma is an exceedingly rare thymic neoplasm with only five reports in English literature to date. We report another patient, a 36-year-old male, who developed local recurrences 4-years after initial resection. The clinicopathologic features of the present and previously reports were compared with particular emphasis on their morphologic spectrum and differential diagnosis.\",\"PeriodicalId\":436929,\"journal\":{\"name\":\"The Annals of thoracic surgery\",\"volume\":\"28 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Annals of thoracic surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32388/hgk9ui\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Annals of thoracic surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32388/hgk9ui","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Thymoliposarcoma is an exceedingly rare thymic neoplasm with only five reports in English literature to date. We report another patient, a 36-year-old male, who developed local recurrences 4-years after initial resection. The clinicopathologic features of the present and previously reports were compared with particular emphasis on their morphologic spectrum and differential diagnosis.