Suppr超能文献

一名38岁女性产后四周,诊断为妊娠性绒毛膜癌,国际妇产科联盟(FIGO)分期为III期,评分8分(高危)。

Gestational choriocarcinoma FIGO stage III, score 8 (high-risk) in 38-year-old woman four weeks postpartum.

作者信息

Illi Clara, Henrich Wolfgang, Hinkson Larry

机构信息

Department of Obstetrics, Charité University Hospital, Berlin, Germany.

出版信息

Case Rep Perinat Med. 2025 Jun 12;14(1):20240041. doi: 10.1515/crpm-2024-0041. eCollection 2025 Jan.

Abstract

OBJECTIVES

Choriocarcinoma, an aggressive form of gestational trophoblastic neoplasia, can be divided into gestational and non-gestational types, each with distinct biological activity and prognosis. We report a case of gestational choriocarcinoma.

CASE PRESENTATION

A 38-year-old woman (2 Gravida, 2 Para) presented at our clinic four weeks after her second cesarean section with persistent vaginal bleeding and decreasing hemoglobin to 6.8 mg/L. In the ultrasound examination, retained placental tissue was suspected. Since conservative management with misoprostol was not effective, a curettage was performed. The histopathological result revealed a gestational choriocarcinoma invading the myometrium (CK18 positive, HPL positive, beta-hCG positive, p63 negative, PLAP positive, Ki67 (MIB-1)>80 %). Beta-hCG was 50,607 IU/L at the time of diagnosis. The computed tomography (CT) scan revealed bilateral pulmonary metastases. There were no metastases to the liver, lymph nodes, skeleton or brain. In accordance with FIGO recommendations [stage III, Score 8 (high risk) choriocarcinoma] a multi-drug chemotherapy after EMACO-regimen was started 9.5 weeks postpartum during 14 days for seven cycles. The patient has been in tumor remission since then.

CONCLUSIONS

Choriocarcinoma is a differential diagnosis of vaginal peripartum bleeding and might likely be underdiagnosed. Risk factors like a prior hydatidiform mole or abortion, Asian, Indian American, African American or Hispanic ethnicity, advanced maternal age (>40 years), blood group A, or high/increasing beta-hCG postpartum should be taken into consideration.

摘要

目的

绒毛膜癌是妊娠滋养细胞肿瘤的一种侵袭性形式,可分为妊娠性和非妊娠性类型,每种类型具有不同的生物学活性和预后。我们报告一例妊娠性绒毛膜癌病例。

病例介绍

一名38岁女性(孕2产2)在第二次剖宫产术后四周因持续阴道出血且血红蛋白降至6.8mg/L前来我院就诊。超声检查怀疑有胎盘组织残留。由于米索前列醇保守治疗无效,遂行刮宫术。组织病理学结果显示为侵袭子宫肌层的妊娠性绒毛膜癌(细胞角蛋白18阳性、人胎盘催乳素阳性、β-人绒毛膜促性腺激素阳性、p63阴性、胎盘碱性磷酸酶阳性、Ki67(MIB-1)>80%)。诊断时β-人绒毛膜促性腺激素为50607IU/L。计算机断层扫描(CT)显示双侧肺转移。无肝、淋巴结、骨骼或脑转移。根据国际妇产科联盟(FIGO)的建议[Ⅲ期,评分8(高危)绒毛膜癌],在产后9.5周开始采用EMACO方案进行多药化疗,为期14天,共七个周期。此后患者一直处于肿瘤缓解状态。

结论

绒毛膜癌是产后阴道出血的鉴别诊断之一,可能容易被漏诊。应考虑既往葡萄胎或流产史、亚洲、印度裔美国人、非裔美国人或西班牙裔种族、高龄产妇(>40岁)、血型A或产后β-人绒毛膜促性腺激素高/升高等高风险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a75/12165762/2bb6a1c4a324/j_crpm-2024-0041_fig_002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验