Epithelioid trophoblastic tumor

Epithelioid trophoblastic tumor
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DOI:
10.1016/j.tjog.2015.08.020
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发表时间:
2015-10-01
影响因子:
2.1
通讯作者:
Karadayi, Nimet
Karadayi, Nimet
中科院分区:
医学4区
文献类型:
--
作者:
Keser, Sevinc Hallac;Kokten, Sermin Coban;Karadayi, Nimet

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目的:描述一例绝经后妇女的上皮样滋养细胞瘤(ETT),其具有与先前报道的ETT不同的几个特殊特征。病例报告:子宫ETT是一种罕见的滋养细胞肿瘤,至今仅有100例。我们的病例不同于以前报道的病例,因为它有几个特殊的特征。本例患者无滋养细胞或妇科疾病病史;绝经后;一开始就有宫颈内伸;随访时复发及转移;Ki-67指数高,人绒毛膜促性腺激素值正常。结论:由于准确的鉴别诊断将改变治疗方法和预后,治疗医生有必要了解这些不寻常的表现。版权所有:台湾妇产科学协会。爱思唯尔台湾有限责任公司出版,版权所有。
Objective: To describe a case of epithelioid trophoblastic tumor (ETT) in a postmenopausal woman, which had several peculiar features that differentiate it from previously reported ETTs.Case report: ETT of the uterus is a rare form of trophoblastic tumor with only 100 cases distinguished until now. Our case differs from the previously reported ones due to its several exceptional features. Our patient had no history of trophoblastic or gynecological disease; is postmenopausal; had endocervical extension from the beginning; recurrences and metastasis at follow up; and had a high Ki-67 index and a normal beta-human chorionic gonadotropin value.Conclusion: Because precise differential diagnosis will alter the therapeutic approach and prognosis, it is necessary for treating physicians to be aware of these unusual presentations. Copyright (C) 2015, Taiwan Association of Obstetrics & Gynecology. Published by Elsevier Taiwan LLC. All rights reserved.