Malignant recurrent orbital solitary fibrous tumor.

IF 0.8 4区 医学 Q4 PATHOLOGY Indian Journal of Pathology and Microbiology Pub Date : 2023-10-01 DOI:10.4103/ijpm.ijpm_713_21
Jaydeep N Pol, Dipti B Patil, Sharad S Desai, Adnan B Calcuttawala
{"title":"Malignant recurrent orbital solitary fibrous tumor.","authors":"Jaydeep N Pol, Dipti B Patil, Sharad S Desai, Adnan B Calcuttawala","doi":"10.4103/ijpm.ijpm_713_21","DOIUrl":null,"url":null,"abstract":"<p><p>Solitary fibrous tumor (SFT) is a rare mesenchymal tumor of fibroblastic origin commonly occurring in pleura. It can occur at many extrapleural sites but is rare in orbit. Most cases are benign and recurrence is not unusual in the head and neck and orbit and is usually due to incomplete surgical excision. However, malignant transformation (MT) in orbital SFT is extremely unusual. We present a case of orbital SFT in adult male who developed recurrence with MT eight years after initial surgical excision. He underwent left orbital exenteration. The recurrent tumor revealed features of malignancy with areas exhibiting morphology typical of SFT. The immunochemistry confirmed the diagnosis of SFT with MT. The patient was given adjuvant radiation and was disease free for the last 18 months. Identification of malignancy in orbital SFT is important for the patient to receive appropriate postoperative treatment, as seen in the present case.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":0.8000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Pathology and Microbiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4103/ijpm.ijpm_713_21","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Solitary fibrous tumor (SFT) is a rare mesenchymal tumor of fibroblastic origin commonly occurring in pleura. It can occur at many extrapleural sites but is rare in orbit. Most cases are benign and recurrence is not unusual in the head and neck and orbit and is usually due to incomplete surgical excision. However, malignant transformation (MT) in orbital SFT is extremely unusual. We present a case of orbital SFT in adult male who developed recurrence with MT eight years after initial surgical excision. He underwent left orbital exenteration. The recurrent tumor revealed features of malignancy with areas exhibiting morphology typical of SFT. The immunochemistry confirmed the diagnosis of SFT with MT. The patient was given adjuvant radiation and was disease free for the last 18 months. Identification of malignancy in orbital SFT is important for the patient to receive appropriate postoperative treatment, as seen in the present case.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
恶性复发性眼眶单发纤维瘤。
孤立性纤维瘤(SFT)是一种罕见的间叶性纤维肿瘤,常发生于胸膜。它可发生在胸膜外的许多部位,但在眼眶内罕见。大多数病例为良性,在头颈部和眼眶复发并不罕见,通常是由于手术切除不彻底所致。然而,眼眶 SFT 的恶性转化(MT)却极为罕见。我们报告了一例成年男性眼眶 SFT 病例,他在初次手术切除八年后复发并伴有 MT。他接受了左眼眶外扩张术。复发的肿瘤显示出恶性肿瘤的特征,其区域呈现出典型的 SFT 形态。免疫化学确诊为 SFT 伴 MT。患者接受了辅助放射治疗,在过去的18个月中一直没有患病。如本病例所示,眼眶 SFT 中恶性肿瘤的鉴别对于患者接受适当的术后治疗非常重要。
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 去求助
来源期刊
CiteScore
1.20
自引率
0.00%
发文量
422
审稿时长
1 months
期刊介绍: The journal will cover studies related to pathology including morbid anatomy, surgical pathology, clinical pathology, diagnostic cytopathology including gynecologic cytology and aspiration cytology, hematology including immuno-hematology and medical microbiology. The journal gives preference to clinically oriented studies over experimental and animal studies. The Journal would publish peer-reviewed original research papers, case reports, systematic reviews, meta-analysis, letters to the editor and brief communications. Review articles on current topics usually are invited by the editor.
期刊最新文献
Low-grade fibromyxoid sarcoma of the maxilla: A diagnosis not to be missed Ischemic fasciitis scalp-unusual presentation and location. Post-mortem detection of a calcifying fibrous pseudotumor at a rare site-A case report. Mesenchymal chondrosarcoma with rhabdomyoblastic differentiation: A malignant round cell tumor with enigmatic immunohistochemical profile. Burnt out testicular tumor - A case report.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1