Extraosseous Primary Ewing's Sarcoma of the Lungs Mistakenly Diagnosed and Managed as Hemothorax: An Extremely Aggressive and Fatal Rare Tumor with an Unusual Site

A. Osman, Ibrahim Mohamed Hirsi, Mohamed Osman Dahir, Ahmed Abdirahman Hussein, A. Bashir
{"title":"Extraosseous Primary Ewing's Sarcoma of the Lungs Mistakenly Diagnosed and Managed as Hemothorax: An Extremely Aggressive and Fatal Rare Tumor with an Unusual Site","authors":"A. Osman, Ibrahim Mohamed Hirsi, Mohamed Osman Dahir, Ahmed Abdirahman Hussein, A. Bashir","doi":"10.58322/stmj.v2i2.23","DOIUrl":null,"url":null,"abstract":"Extraosseous Ewing's sarcoma of the lungs is a rare soft tissue tumor of children and adolescents usually found in the extremities. In this case report, we present a 4-year-old male child with primary Ewing Sarcoma of the lungs who presented with shortness of breath, cough, left-side chest pain, and hemoptysis for two months. We reviewed clinical, radiological, and pathological findings for this rare malignancy.","PeriodicalId":122824,"journal":{"name":"Somalia Turkiye Medical Journal (STMJ)","volume":"34 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Somalia Turkiye Medical Journal (STMJ)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.58322/stmj.v2i2.23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Extraosseous Ewing's sarcoma of the lungs is a rare soft tissue tumor of children and adolescents usually found in the extremities. In this case report, we present a 4-year-old male child with primary Ewing Sarcoma of the lungs who presented with shortness of breath, cough, left-side chest pain, and hemoptysis for two months. We reviewed clinical, radiological, and pathological findings for this rare malignancy.
肺骨外原发性尤文氏肉瘤误诊为血胸:一种具有异常部位的极具侵袭性和致命性的罕见肿瘤
肺骨外尤文氏肉瘤是一种罕见的儿童和青少年软组织肿瘤,通常发现于四肢。在这个病例报告中,我们报告了一个4岁的男孩,他患有原发性肺尤文氏肉瘤,表现为呼吸急促,咳嗽,左侧胸痛和咯血两个月。我们回顾了这种罕见恶性肿瘤的临床、放射学和病理表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信