Sandeep Rana, Robin Choudhary, M. Kirti, Deepak Mulajkar, S. Shivani
{"title":"一个罕见的骨外尤文氏肉瘤病例","authors":"Sandeep Rana, Robin Choudhary, M. Kirti, Deepak Mulajkar, S. Shivani","doi":"10.4103/jacp.jacp_1_24","DOIUrl":null,"url":null,"abstract":"Ewing’s sarcoma (ES) is a rare and highly aggressive tumour of neuroectodermal origin. Primary pulmonary ES is extremely rare and difficult to distinguish from other lung tumours due to its similar presentation and nonspecific symptoms. It requires a deliberate interplay of imaging, histopathological exam, immunohistochemistry (IHC) and genetic analysis to confirm the diagnosis. Here we present a rare case of extra osseus ES.","PeriodicalId":30411,"journal":{"name":"The Journal of Association of Chest Physicians","volume":"30 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A rare case of extraosseous Ewing’s sarcoma\",\"authors\":\"Sandeep Rana, Robin Choudhary, M. Kirti, Deepak Mulajkar, S. Shivani\",\"doi\":\"10.4103/jacp.jacp_1_24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ewing’s sarcoma (ES) is a rare and highly aggressive tumour of neuroectodermal origin. Primary pulmonary ES is extremely rare and difficult to distinguish from other lung tumours due to its similar presentation and nonspecific symptoms. It requires a deliberate interplay of imaging, histopathological exam, immunohistochemistry (IHC) and genetic analysis to confirm the diagnosis. Here we present a rare case of extra osseus ES.\",\"PeriodicalId\":30411,\"journal\":{\"name\":\"The Journal of Association of Chest Physicians\",\"volume\":\"30 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Association of Chest Physicians\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/jacp.jacp_1_24\",\"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 Journal of Association of Chest Physicians","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jacp.jacp_1_24","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Ewing’s sarcoma (ES) is a rare and highly aggressive tumour of neuroectodermal origin. Primary pulmonary ES is extremely rare and difficult to distinguish from other lung tumours due to its similar presentation and nonspecific symptoms. It requires a deliberate interplay of imaging, histopathological exam, immunohistochemistry (IHC) and genetic analysis to confirm the diagnosis. Here we present a rare case of extra osseus ES.
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