原发于卵巢的纯原发性非妊娠期绒毛膜癌1例报告并文献复习。

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2021-10-08 eCollection Date: 2021-01-01 DOI:10.1177/20363613211052506
Xiujie Yu, Qiuyue Du, Xiaojing Zhang, Yixin Liu, Yan Shen
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引用次数: 6

摘要

卵巢非妊娠期绒毛膜癌(NGCO)是罕见的,患病率低于0.6%的所有卵巢生殖细胞肿瘤;在其他生殖细胞肿瘤中,纯NGCO是非常罕见的。我们在此报告的情况下,22岁的妇女谁抱怨月经紊乱超过2个月。MRI示右侧子宫附件肿块11.4 cm,血清β-hCG水平升高77,928 mIU/ml。行保生育手术,病理诊断为纯NGCO;免疫组化染色显示癌细胞β-hCG、CK、hPL、SALL4和Ki-67阳性(>80%的细胞染色)。我们进行了多态性DNA分析,证实了非妊娠起源。患者接受6个疗程的BEP方案化疗,术后血清β-hCG水平降至正常水平,随访30个月无疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Pure primary non-gestational choriocarcinoma originating in the ovary: A case report and literature review.

Non-gestational choriocarcinoma (NGCO) of the ovary is rare, with a prevalence of less than 0.6% of all ovarian germ-cell tumors; and when found with other germ cell tumors, pure NGCO is exceedingly rare. We herein report the case of a 22-year-old woman who complained of menstrual disorders for over 2 months. MRI examination revealed an 11.4 cm right adnexal mass of the uterus, and the patients manifested an elevated serum level of β-hCG of 77,928 mIU/ml. Fertility-preserving surgery was performed, and the pathologic diagnosis was pure NGCO; immunohistochemical staining showed cancer cells that were positive for β-hCG, CK, hPL, SALL4, and Ki-67 (>80% of cells stained). We performed polymorphic DNA analysis and non-gestational origin was confirmed. The patient was then treated with six courses of chemotherapy with a BEP regimen, after which her serum β-hCG levels declined to normal levels, and she was free of disease at the 30-month follow-up.

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Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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