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作 者:Hani Maalouf Ribal Aby Hadeer Souad Ghattas Omar Tabbikha Hasan Numan Raja Wakim
机构地区:[1]Department of General Surgery,University of Balamand,Beirut 100,Lebanon [2]Department of General Surgery,Mount Lebanon Hospital University Medical Center,Beirut 7031,Lebanon
出 处:《World Journal of Clinical Cases》2024年第25期5791-5797,共7页世界临床病例杂志
摘 要:BACKGROUND Solitary fibrous tumor(SFT)is a remarkably uncommon mesenchymal tumor.STAT6 level and a combination of clinical,pathological,and molecular features are required to arrive at a proper diagnosis.CASE SUMMARY In this report,we present an intriguing case involving a 43-year-old woman who initially exhibited symptoms of a bleeding retroperitoneal tumor,initially resembling a gastrointestinal stromal tumor,but later confirmed as an SFT.However,a year later,what was initially believed to be a recurrence of her SFT was instead identified as a desmoid tumor.CONCLUSION Distinguishing SFT from other tumors was pivotal.Correcting misdiagnoses of tumor type initially and of recurrence later was necessary for appropriate treatment of the correct desmoid type.
关 键 词:Solitary fibrous tumor Retroperitoneal tumor Soft tissue neoplasms SARCOMA NAB2-STAT6 Case report
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