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BMJ Case Rep. 2020 Jul 9;13(7):e234757. doi: 10.1136/bcr-2020-234757.
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本文引用的文献

1
Spindle cell sarcoma: a SEER population-based analysis.梭形细胞肉瘤:一项 SEER 基于人群的分析。
Sci Rep. 2018 Mar 22;8(1):5024. doi: 10.1038/s41598-018-23145-4.
2
Genomics of a pediatric ovarian fibrosarcoma. Association with the DICER1 syndrome.儿童卵巢纤维肉瘤的基因组学。与 DICER1 综合征相关。
Sci Rep. 2018 Feb 19;8(1):3252. doi: 10.1038/s41598-018-21663-9.
3
Current diagnostics and treatment of fibrosarcoma -perspectives for future therapeutic targets and strategies.纤维肉瘤的当前诊断与治疗——未来治疗靶点与策略的展望
Oncotarget. 2017 Aug 10;8(61):104638-104653. doi: 10.18632/oncotarget.20136. eCollection 2017 Nov 28.
4
Primary ovarian fibrosarcoma: a case report and review of the literature.原发性卵巢纤维肉瘤:一例病例报告及文献复习
J Exp Ther Oncol. 2016 Jul;11(3):225-235.
5
Ovarian fibrosarcoma: case report and latest trends in diagnostic and therapeutic management.卵巢纤维肉瘤:病例报告及诊断与治疗管理的最新趋势
Eur J Gynaecol Oncol. 2015;36(6):742-5.
6
Gynecologic Cancer InterGroup (GCIG) consensus review for ovarian sex cord stromal tumors.妇科肿瘤研究组(GCIG)关于卵巢性索间质肿瘤的共识综述。
Int J Gynecol Cancer. 2014 Nov;24(9 Suppl 3):S42-7. doi: 10.1097/IGC.0000000000000249.
7
Giant primary ovarian fibrosarcoma: Case report and review of pitfalls.巨大原发性卵巢纤维肉瘤:病例报告及陷阱回顾
J Cytol. 2012 Oct;29(4):255-7. doi: 10.4103/0970-9371.103946.
8
Clinicopathologic characteristics and prognostic factors of ovarian fibrosarcoma: the results of a multi-center retrospective study.卵巢纤维肉瘤的临床病理特征和预后因素:一项多中心回顾性研究的结果。
BMC Cancer. 2010 Oct 27;10:585. doi: 10.1186/1471-2407-10-585.
9
Ovarian Fibrosarcoma: Clinicopathologic Considerations about the Intraoperative and Post-Surgical Procedures.卵巢纤维肉瘤:关于术中及术后操作的临床病理考量
Case Rep Med. 2009;2009:802817. doi: 10.1155/2009/802817. Epub 2010 Feb 7.
10
Sarcomas with spindle cell morphology.具有梭形细胞形态的肉瘤。
Semin Oncol. 2009 Aug;36(4):324-37. doi: 10.1053/j.seminoncol.2009.06.007.

46 岁女性在接受最佳减瘤手术后迅速复发卵巢纤维肉瘤。

Rapidly recurring ovarian fibrosarcoma after optimal debulking surgery in a 46-year-old woman.

机构信息

Department of Obstetrics and Gynaecology, Dr Cipto Mangunkusumo Hospital, Central Jakarta, Indonesia

Faculty of Medicine, Universitas Indonesia, Central Jakarta, Indonesia.

出版信息

BMJ Case Rep. 2020 Jul 9;13(7):e234757. doi: 10.1136/bcr-2020-234757.

DOI:10.1136/bcr-2020-234757
PMID:32646936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7351292/
Abstract

Ovarian fibrosarcoma is an extremely rare tumour with no universally accepted guidelines for treatment. We present a 46-year-old nulliparous woman with ovarian fibrosarcoma who mainly presented with a painful abdominal enlargement. Optimal debulking surgery was performed, and a specimen of the tumour was examined. A frozen section examined during surgery revealed spindle cell morphology, raising the suspicion of ovarian fibrosarcoma, which was later confirmed by immunohistochemistry staining. Our patient refused to undergo chemotherapy and died 3 months after surgery due to tumour recurrence. Although no clear consensus exists for administering chemotherapy for fibrosarcoma, some published case reports have shown a lower chance of recurrence and better prognosis in patients who undergo chemotherapy compared with our patient.

摘要

卵巢纤维肉瘤是一种极其罕见的肿瘤,目前尚无普遍接受的治疗指南。我们报告了一例 46 岁的未产妇,主要表现为腹痛性腹部增大。进行了最佳的肿瘤细胞减灭术,并对肿瘤标本进行了检查。术中冷冻切片检查显示梭形细胞形态,提示卵巢纤维肉瘤,随后通过免疫组织化学染色得到证实。我们的患者拒绝接受化疗,术后 3 个月因肿瘤复发死亡。虽然对于纤维肉瘤是否进行化疗尚未达成明确共识,但一些已发表的病例报告显示,与我们的患者相比,接受化疗的患者复发机会更低,预后更好。