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Primary yolk sac tumor of the endometrium: a case report and review of the literatures

机译:子宫内膜的主要蛋黄囊肿瘤:一个案例报告和文献审查

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Purpose 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. Methods 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. Results 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. Conclusion 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.
机译:目的yolk sac肿瘤(YST)是衍生自生殖细胞的恶性肿瘤,并且通常发生在GONADS中。额外的Gonadal YST是最常见的儿童阴道,但很少在子宫颈,外阴和子宫内膜中。子宫内膜的主要YST非常罕见,标准治疗仍然存在争议,到目前为止没有建立指导。本研究的目的是为管理子宫内膜的主要YST提供全面的理解和系统思维。方法在Scopus,Pubmed数据库和Cochrane图书馆进行文献的系统研究,包括案例报告和案例系列。我们总结了所有收集病例的临床特征,治疗和预后。我们收集了有关患者,血清AFP水平,初始症状,手术信息,术后化疗和放射疗法的数据。还讨论了一个新案例。结果我们发现尚未报告26例。我们报告了一个27岁的女性中初级子宫内膜炎的新案例,在这种情况下,我们创造性地进行了双侧卵巢保存和使用的DC(多西紫杉醇和卡铂)术后化疗方案,我们在此期间取得了相对良好的预后随访时间为14个月。结论子宫内膜的主要YST,一种高度恶性生殖细胞肿瘤,非常罕见,其中初始症状通常是阴道出血异常。标准治疗仍然存在争议,到目前为止没有建立指导。与术后化疗结合的手术被认为是治疗原代子宫内膜YST的有效。关于是否在早期阶段保存卵巢的决定需要仔细考虑,全面的术前评估和全面的沟通。建议术中活组织检查和严格的术后随访。然而,术后放疗的标准化疗方案及可行性仍有待讨论。

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