1例实现R0切除但快速进展伴脑转移的晚期 卵巢未分化肉瘤及其文献复习
A Case of Advanced Undifferentiated Ovarian Sarcoma with Rapid Progression and Brain Metastasis after R0 Resection and Literature Review
DOI: 10.12677/acm.2026.1652147, PDF,    科研立项经费支持
作者: 刘印美, 谢贝贝*, 张海燕, 吴 怡, 孔 悦:临沂市人民医院妇科一病区,山东 临沂;孙 雪:临沂市人民医院病理科,山东 临沂;周士娟:临沂市人民医院影像科,山东 临沂;郭玲娣:临沂市人民医院产科六病区,山东 临沂
关键词: 卵巢未分化肉瘤卵巢肉瘤免疫组织化学诊断鉴别诊断手术治疗Undifferentiated Ovarian Sarcoma Ovarian Sarcoma Immunohistochemistry Diagnosis Differential Diagnosis Surgical Treatment
摘要: 卵巢未分化肉瘤(Undifferentiated Ovarian Sarcoma, UOS)是一种起源于卵巢间质的高度恶性肿瘤,极为罕见,国内外仅以个案报道出现。其临床表现缺乏特异性,侵袭性强,预后差,早期难以识别,确诊主要依靠病理形态学及免疫组化检查。目前治疗上尚无标准的治疗方案,一般借鉴卵巢上皮性癌(Ovarian cancer, OC)的治疗原则。本文报道1例晚期卵巢未分化肉瘤患者,初次治疗行肿瘤细胞减灭术并达到R0切除,术后补充紫杉醇 + 表柔比星方案6周期化疗,最后因脑转移死亡,总生存期限11个月。现将其诊治过程结合相关文献进行回顾,旨在提高对本病的认识,减少误诊和漏诊。
Abstract: Undifferentiated ovarian sarcoma (UOS) is a highly malignant tumor derived from ovarian stroma. It is extremely rare and has only been reported in sporadic case reports at home and abroad. This disease presents with non-specific clinical manifestations, high invasiveness and poor prognosis, and is difficult to identify at an early stage. The definitive diagnosis mainly relies on pathological morphology and immunohistochemical examination. At present, there is no standardized therapeutic regimen, and the treatment principles for ovarian epithelial carcinoma (OC) are generally adopted for reference. Herein, we report a case of advanced undifferentiated ovarian sarcoma. The patient underwent primary cytoreductive surgery with successful R0 resection, followed by six cycles of adjuvant chemotherapy with paclitaxel plus epirubicin. Eventually, the patient died of brain metastasis, with an overall survival of 11 months. The diagnosis and treatment process of this case were reviewed in combination with relevant literature, aiming to deepen the understanding of this disease and reduce the incidence of misdiagnosis and missed diagnosis.
文章引用:刘印美, 谢贝贝, 张海燕, 吴怡, 孔悦, 孙雪, 周士娟, 郭玲娣. 1例实现R0切除但快速进展伴脑转移的晚期 卵巢未分化肉瘤及其文献复习[J]. 临床医学进展, 2026, 16(5): 3267-3272. https://doi.org/10.12677/acm.2026.1652147

参考文献

[1] 张鸿瑞, 何春年. 卵巢原发性未分化肉瘤1例及文献复习[J]. 临床与实验病理学杂志, 2009, 25(4): 428-430.
[2] Mekni, K., Mlika, M., Houcine, Y. and ElFekih, C. (2022) Undifferentiated Sarcoma Arising in an Immature Teratoma of the Ovary. International Journal of Surgery Case Reports, 101, Article ID: 107791. [Google Scholar] [CrossRef] [PubMed]
[3] Sood, A.K., Sorosky, J.I., Gelder, M.S., Buller, R.E., Anderson, B., Wilkinson, E.J., et al. (1998) Primary Ovarian Sarcoma. Cancer, 82, 1731-1737. [Google Scholar] [CrossRef] [PubMed]
[4] 谢幸, 苟文丽. 妇产科学[M]. 第8版. 北京: 人民卫生出版社, 2013: 163.
[5] Sahin, A. and Benda, J.A. (1988) An Immunohistochemical Study of Primary Ovarian Sarcoma. An Evaluation of Nine Tumors. International Journal of Gynecological Pathology, 7, 268-279. [Google Scholar] [CrossRef] [PubMed]
[6] WHO Classification of Tumours Editorial Board (2020) WHO Classification of Tumours: Female Genital Tumours. IARC Publications, 1-26, 32.
[7] Prat, J. (2015) Staging Classification for Cancer of the Ovary, Fallopian Tube, and Peritoneum: Abridged Republication of Guidelines From the International Federation of Gynecology and Obstetrics (FIGO). Obstetrics & Gynecology, 126, 171-174. [Google Scholar] [CrossRef] [PubMed]
[8] 迪娜∙海沙尔, 周绍波, 陈放, 等. 原发性卵巢血管肉瘤的研究进展[J]. 中华妇产科杂志, 2023, 58(12): 957-960.
[9] Peng, X., Duan, Z., Yin, H., Dai, F. and Liu, H. (2021) Ovarian Epithelioid Angiosarcoma Complicating Pregnancy: A Case Report and Review of the Literature. Journal of International Medical Research, 49, 1-8. [Google Scholar] [CrossRef] [PubMed]
[10] Dundar, B., Alrwashdeh, A. and Dahmoush, L. (2023) Tumor to Tumor Metastasis: A Case Report of Metastatic Angiosarcoma to an Ovarian Brenner Tumor and Review of the Literature. International Journal of Gynecological Pathology, 42, 176-181. [Google Scholar] [CrossRef] [PubMed]
[11] 张嫱, 张京顺, 郑连文. 老年女性原发性卵巢平滑肌肉瘤临床特征及诊断研究进展[J]. 中国老年学杂志, 2023, 43(5): 1260-1263.
[12] Bennett, J.A. and Oliva, E. (2021) Undifferentiated and Dedifferentiated Neoplasms of the Female Genital Tract. Seminars in Diagnostic Pathology, 38, 137-151. [Google Scholar] [CrossRef] [PubMed]
[13] Thankamony, P., Chandar, R., Kattoor, J. and Nair, R.K. (2018) Pediatric Primary Ovarian Angiosarcoma: From Rarity to a Realization. Journal of Pediatric and Adolescent Gynecology, 31, 629-631. [Google Scholar] [CrossRef] [PubMed]
[14] Buza, N. (2019) Frozen Section Diagnosis of Ovarian Epithelial Tumors: Diagnostic Pearls and Pitfalls. Archives of Pathology & Laboratory Medicine, 143, 47-64. [Google Scholar] [CrossRef] [PubMed]
[15] 中国医师协会整合医学分会妇产疾病整合专业委员会, 中国医师协会微无创专业委员会妇科肿瘤学组. 妇科手术术前评估与准备的中国专家共识(2022年版) [J]. 中国实用妇科与产科杂志, 2022, 38(6): 622-627.
[16] 余健, 张国楠. 原发性卵巢肉瘤[J]. 四川肿瘤防治, 2000(1): 62-64.
[17] Rogawski, D., Wheeler, J., Nie, E., Zhu, W., Villanueva, E., Coffey, G., et al. (2024) A Rare Non-Gadolinium Enhancing Sarcoma Brain Metastasis with Microenvironment Dominated by Tumor-Associated Macrophages. Acta Neuropathologica Communications, 12, Article No. 15. [Google Scholar] [CrossRef] [PubMed]
[18] Trozzi, R., Salvi, M., Karimi, M., Minucci, A., Raspaglio, G., De Donato, M., et al. (2026) Deciphering Brain Metastasis in Epithelial Ovarian Cancer: Multimodal Analysis and Potential Biomarkers. npj Precision Oncology, 10, Article No. 83. [Google Scholar] [CrossRef
[19] Jackson, G.A. and Adamson, D.C. (2025) Similarities in Mechanisms of Ovarian Cancer Metastasis and Brain Glioblastoma Multiforme Invasion Suggest Common Therapeutic Targets. Cells, 14, Article 171. [Google Scholar] [CrossRef] [PubMed]
[20] van der Laan, P., van Houdt, W.J., van Boven, H., Snaebjornsson, P., Bosch, L.J.W., Monkhorst, K., et al. (2025) The Role of Whole-Genome Sequencing for Guiding Systemic Therapy in Patients with Soft Tissue Sarcoma. ESMO Open, 10, Article ID: 105287. [Google Scholar] [CrossRef] [PubMed]