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两例绝经后妇女的上皮样滋养细胞肿瘤

Two cases of epithelioid trophoblastic tumors in postmenopausal women.

作者信息

Rodríguez-Trujillo Adriano, Martínez-Serrano María José, Saco Adela, Torné Aureli

机构信息

1Department of Gynecology and Obstetrics, Hospital Clìnic i Provincial, University of Barcelona, Spain 2Department of Pathology, Hospital Clínic i Provincial, University of Barcelona, Spain.

出版信息

Menopause. 2017 Nov;24(11):1304-1308. doi: 10.1097/GME.0000000000000908.

Abstract

OBJECTIVE

Epithelioid trophoblastic tumor is a rare gestational trophoblastic neoplasm usually presenting in women of reproductive age, with a history of a prior gestational event. Its presentation in postmenopausal women is extremely rare. Immunohistochemical staining is a helpful aid to distinguish epithelioid trophoblastic tumor from other gestational trophoblastic neoplasms. Correct diagnosis is crucial for clinical management that can vary according to the type of gestational trophoblastic neoplasm.

METHODS

We report the case of a 63-year-old postmenopausal woman 33 years after her last full-term pregnancy and another case of a 57-year-old postmenopausal woman who had had a first-trimester abortion 30 years previously as her last gestational event, both presenting cervical epithelioid trophoblastic tumors. In both cases, immunohistochemistry played an important role in differentiating this entity from other gestational trophoblastic neoplasms. Surgery was the primary treatment in both cases. The first patient remained disease-free and died 5 years later due to a rectal adenocarcinoma, and the second patient remains disease-free at publication.

RESULTS

In both cases, the hysterectomy specimen confirmed the presence of two large epithelioid trophoblastic tumors arising in the endocervix and lower uterine segment with no extrauterine disease. Nuclear positivity for p63 allowed differentiation from a placental site trophoblastic tumor. The Ki67 proliferative index was 20% and 35%, respectively.

CONCLUSIONS

Epithelioid trophoblastic tumors may occur a long time after a prior gestational event and should even be excluded in postmenopausal women with uterine masses. Immunohistochemical staining is helpful to make the differential diagnosis with other gestational trophoblastic neoplasms.

摘要

目的

上皮样滋养细胞肿瘤是一种罕见的妊娠滋养细胞肿瘤,通常发生于育龄期妇女,有既往妊娠史。其在绝经后妇女中极为罕见。免疫组织化学染色有助于将上皮样滋养细胞肿瘤与其他妊娠滋养细胞肿瘤区分开来。正确诊断对于临床管理至关重要,临床管理会因妊娠滋养细胞肿瘤的类型而异。

方法

我们报告了一例63岁绝经后妇女,其末次足月妊娠33年后发病,以及另一例57岁绝经后妇女,其末次妊娠为30年前的早期流产,这两例均表现为宫颈上皮样滋养细胞肿瘤。在这两例中,免疫组织化学在将该实体与其他妊娠滋养细胞肿瘤区分开来方面发挥了重要作用。手术是这两例的主要治疗方法。第一例患者无疾病复发,5年后因直肠腺癌死亡,第二例患者在发表本文时仍无疾病复发。

结果

在这两例中,子宫切除标本均证实宫颈管和子宫下段存在两个大的上皮样滋养细胞肿瘤,无子宫外病变。p63核阳性有助于与胎盘部位滋养细胞肿瘤相鉴别。Ki67增殖指数分别为20%和35%。

结论

上皮样滋养细胞肿瘤可能在既往妊娠事件后很长时间发生,甚至绝经后子宫肿块的妇女也应排除该病。免疫组织化学染色有助于与其他妊娠滋养细胞肿瘤进行鉴别诊断。

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