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原发性卵巢血管肉瘤:诊断挑战与难题

Primary Ovarian Angiosarcoma: Diagnostic Challenges and Conundrums.

作者信息

Agrawal Sujata, Chowdhury Zachariah, Jethani Roma

机构信息

Department of Oncopathology Homi Bhabha Cancer Hospital (HBCH) and Mahamana Pandit Madan Mohan Malviya Cancer Centre (MPMMCC), Tata Memorial Centre, Homi Bhabha National Institute (HBNI), Varanasi, India.

出版信息

Discoveries (Craiova). 2024 Dec 31;12(4):e198. doi: 10.15190/d.2024.17. eCollection 2024 Oct-Dec.

DOI:10.15190/d.2024.17
PMID:39845895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11746002/
Abstract

Angiosarcoma is an extremely uncommon mesenchymal neoplasm overall and moreso in female genital organs such as the ovary. Diagnosing primary ovarian angiosarcoma remains challenging on clinical grounds due to the absence of specific clinical symptoms as well as on histopathological analysis especially in poorly differentiated subtypes due to non-specific and overlapping morphologic features. Misdiagnosis in such scenarios can be devastating as this tumor is clinically very aggressive. We describe a case of primary ovarian angiosarcoma in a 33-year-old multiparous female with bilateral ovarian masses and metastasis at diagnosis. Histopathologic appraisal revealed a poorly differentiated malignant tumor with varied differential diagnoses. The saviour in such a scenario was the immunohistochemistry findings, underlining the incredible utility of this technique in the precise diagnosis and evasion of misdiagnosis. This case accentuates the paramount importance of precise diagnostic modalities in shaping clinical practice and enriching the scientific understanding of rare and aggressive neoplasms. Against this backdrop, the potential pitfalls and pearls while dealing with this entity have been elucidated, along with a review of the recent literature.

摘要

血管肉瘤总体上是一种极其罕见的间叶性肿瘤,在女性生殖器官如卵巢中更为罕见。由于缺乏特异性临床症状,以及在组织病理学分析中,尤其是在低分化亚型中,由于形态学特征不特异且相互重叠,诊断原发性卵巢血管肉瘤在临床上仍然具有挑战性。在这种情况下误诊可能是灾难性的,因为这种肿瘤在临床上具有很强的侵袭性。我们描述了一例33岁经产妇原发性卵巢血管肉瘤病例,诊断时双侧卵巢有肿块并伴有转移。组织病理学评估显示为低分化恶性肿瘤,鉴别诊断多样。在这种情况下,免疫组化结果起到了关键作用,凸显了该技术在精确诊断和避免误诊方面的巨大效用。该病例强调了精确诊断方法在指导临床实践和丰富对罕见侵袭性肿瘤的科学认识方面的至关重要性。在此背景下,阐明了处理该实体时潜在的陷阱和要点,并对近期文献进行了综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c82/11746002/0cee07d2b1e8/discoveries-12-198-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c82/11746002/0cee07d2b1e8/discoveries-12-198-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c82/11746002/0cee07d2b1e8/discoveries-12-198-g001.jpg

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本文引用的文献

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Angiosarcoma of the ovary treated with polyadenosine ribose polymerase Inhibition, a case report and review of the literature.聚腺苷酸核糖聚合酶抑制治疗卵巢血管肉瘤:一例报告并文献复习
Gynecol Oncol Rep. 2023 Aug 23;49:101264. doi: 10.1016/j.gore.2023.101264. eCollection 2023 Oct.
2
Primary ovarian angiosarcoma: Two case reports and review of literature.原发性卵巢血管肉瘤:两例病例报告及文献综述
World J Clin Cases. 2023 Jul 26;11(21):5122-5128. doi: 10.12998/wjcc.v11.i21.5122.
3
Ovarian epithelioid angiosarcoma complicating pregnancy: a case report and review of the literature.
卵巢上皮样血管肉瘤合并妊娠:病例报告及文献复习。
J Int Med Res. 2021 May;49(5):3000605211019641. doi: 10.1177/03000605211019641.
4
Primary ovarian angiosarcoma: a rare and recognizable ovarian tumor.原发性卵巢血管肉瘤:一种罕见且可识别的卵巢肿瘤。
J Ovarian Res. 2021 Jan 28;14(1):21. doi: 10.1186/s13048-021-00771-7.
5
Complete response after MAID treatment for advanced primary ovarian angiosarcoma: case report and literature review.晚期原发性卵巢血管肉瘤经MAID治疗后的完全缓解:病例报告及文献综述
Eur J Gynaecol Oncol. 2014;35(3):318-21.
6
Ovarian angiosarcoma: a case report and review of the literature.卵巢血管肉瘤:一例病例报告及文献综述
J Med Case Rep. 2014 Feb 12;8:47. doi: 10.1186/1752-1947-8-47.
7
Angiosarcoma arising in an ovarian fibroma: a case report.卵巢纤维瘤中发生的血管肉瘤:一例报告
Patholog Res Int. 2010 Oct 31;2010:842592. doi: 10.4061/2010/842592.
8
Human aging and CD31+ T-cell number, migration, apoptotic susceptibility, and telomere length.人类衰老与 CD31+T 细胞数量、迁移、凋亡易感性和端粒长度。
J Appl Physiol (1985). 2010 Dec;109(6):1756-61. doi: 10.1152/japplphysiol.00601.2010. Epub 2010 Sep 23.
9
Immunohistochemical expression of endothelial markers CD31, CD34, von Willebrand factor, and Fli-1 in normal human tissues.内皮标志物CD31、CD34、血管性血友病因子和Fli-1在正常人体组织中的免疫组化表达。
J Histochem Cytochem. 2006 Apr;54(4):385-95. doi: 10.1369/jhc.4A6514.2005. Epub 2005 Oct 18.
10
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Pathol Int. 1998 Dec;48(12):967-73. doi: 10.1111/j.1440-1827.1998.tb03868.x.