子宫碰撞肿瘤。病例报告和文献回顾。

Franco Rafael Ruiz-Echeverría, María Islena Beltrán-Salazar, Lina María Caicedo-Páez, Maribel Palencia-Palacios, Catherin Salazar-Silva, David Viveros-Carreño
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摘要

目的:报告一名子宫碰撞肿瘤患者的病例,并回顾有关该疾病的组织病理诊断、治疗和预后的文献。材料和方法:一名76岁的妇女咨询了哥伦比亚波哥大的国家癌症参考中心,在那里诊断出子宫碰撞肿瘤,由浆液性子宫内膜腺癌和宫颈腺肉瘤组成。他接受了手术治疗加上化疗和补充放疗,16个月后去世。通过PubMed和Embase在Medline数据库中搜索了文献,其中包括诊断为子宫碰撞肿瘤的妇女的报告和病例系列,并提取了有关诊断、治疗和预后的信息。对发现进行了叙述性总结。结果:搜索确定了36个标题,其中包括14项研究,其中包括17名患者。最常见的组织病理诊断是子宫内膜样腺癌和高低级别子宫内膜肉瘤(47%)。基本治疗是外科手术。近50%的人接受了化疗和放疗的辅助治疗(15%)。1年生存率为75%。结论:在文献中,没有发现子宫碰撞肿瘤的病例与组织病理学和出现病例的位置有关。如果考虑到报告的病例,两年死亡率接近28%。需要进行更多的研究来描述这种情况的免疫组化、治疗和预后。
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Uterine collision tumor. Case report and review of the literature

Objectives: To report the case of a patient with a uterine collision tumor and to conduct a review of the literature.

Material and methods: A 76-year-old patient who presented to the national cancer referral center in Bogota (Colombia), where she was diagnosed with a uterine collision tumor consisting of a seroustype endometrial adenocarcinoma and a cervical adenosarcoma. The patient underwent surgical treatment followed by chemotherapy and supplemental radiotherapy, and died 16 months later. A search was conducted in the Medline via PubMed and Embase databases, including reports and case series of women with a diagnosis of uterine collision tumor, with retrieval of information regarding diagnosis, treatment and prognosis. A narrative summary of the findings was made.

Results: The search identified 36 titles, of which 14 studies with 17 patients were included. The most frequent histopathological diagnosis was endometrial adenocarcinoma and high and low grade endometrial sarcoma (47 %). Primary treatment was surgery and adjuvant treatment with chemotherapy and radiotherapy (15 %) was performed in close to 50 % of cases. One-year survival was 75 %.

Conclusions: No cases of uterine collision tumors with the histopathology or in the location of the reported case were found in the literature. If this reported case is taken into account, 2-year mortality is 28 %. Further studies to describe the immunohistochemistry, treatment and prognosis of this condition are needed.

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