Department of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, People's Republic of China.
Arch Gynecol Obstet. 2019 Nov;300(5):1177-1187. doi: 10.1007/s00404-019-05309-3. Epub 2019 Sep 23.
Yolk sac tumor (YST) is a malignant tumor derived from germ cells and usually occurs in the gonads. Extra-gonadal YST is most commonly seen in the vagina of children, but rarely in the cervix, vulva and endometrium. Primary YST of endometrium was extremely rare, standard treatment was still controversial and no guideline was established so far. The aim of the present study was to provide a comprehensive understanding and systematic thought for the management of primary YST of endometrium.
A systematic research of the literature was conducted in Scopus, PubMed database and Cochrane Library, including case reports and case series. We summarized clinical characteristics, treatments and prognosis of all collected cases. We collected data regarding patients, serum AFP level, initial symptoms, surgical information, postoperative chemotherapy and radiotherapy. A new case was also discussed.
We found only 26 cases have been reported previously. We reported a new case of primary endometrial YST in a 27-year-old woman, and in this case, we creatively performed bilaterally ovarian preservation and used DC (docetaxel and carboplatin) regimen of postoperative chemotherapy, we achieved a relatively good prognosis during the follow-up period of 14 months.
Primary YST of endometrium, kind of highly malignant germ cell tumors, was extremely rare, of which initial symptom is usually abnormal vaginal bleeding. Standard treatment was still controversial and no guideline was established so far. Surgery combining with postoperative chemotherapy was considered effective for treatment of primary endometrial YST. Decision on whether to preserve ovaries in young patient with early stage needs careful consideration, comprehensive preoperative assessment and full communication. Intraoperative biopsy and strict postoperative follow-up are recommended. However, standard chemotherapy regimen and feasibility of postoperative radiotherapy remains to be discussed.
卵黄囊瘤(YST)是一种来源于生殖细胞的恶性肿瘤,通常发生在性腺。卵巢外 YST 最常见于儿童阴道,但在宫颈、外阴和子宫内膜中很少见。原发性子宫内膜 YST 极为罕见,标准治疗仍存在争议,迄今尚未制定指南。本研究旨在为子宫内膜原发性 YST 的管理提供全面的理解和系统的思路。
在 Scopus、PubMed 数据库和 Cochrane Library 中进行了系统的文献研究,包括病例报告和病例系列。我们总结了所有收集病例的临床特征、治疗方法和预后。我们收集了患者、血清 AFP 水平、首发症状、手术信息、术后化疗和放疗的数据。还讨论了一个新病例。
我们仅发现之前有 26 例报道。我们报告了 1 例 27 岁女性原发性子宫内膜 YST 的新病例,在该病例中,我们创新性地进行了双侧卵巢保留,并采用术后化疗的 DC(多西他赛和卡铂)方案,在 14 个月的随访期间取得了相对较好的预后。
原发性子宫内膜 YST 是一种高度恶性生殖细胞肿瘤,极为罕见,其首发症状通常为异常阴道出血。标准治疗仍存在争议,迄今尚未制定指南。手术结合术后化疗被认为是治疗原发性子宫内膜 YST 的有效方法。对于早期年轻患者是否保留卵巢的决策需要仔细考虑、全面的术前评估和充分的沟通。建议术中活检和严格的术后随访。然而,标准的化疗方案和术后放疗的可行性仍有待讨论。