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足月分娩完全性葡萄胎并伴有存活胎儿,随后成功治疗母体转移性妊娠滋养细胞疾病。

Term delivery of a complete hydatidiform mole with a coexisting living fetus followed by successful treatment of maternal metastatic gestational trophoblastic disease.

作者信息

Peng Hsiu-Huei, Huang Kuan-Gen, Chueh Ho-Yen, Adlan Aizura-Syafinaz, Chang Shuenn-Dyn, Lee Chyi-Long

机构信息

Department of Obstetrics and Gynecology, Chang Gung Memorial Hospital, Linkou Medical Center and Chang Gung University College of Medicine, Kwei-Shan, Taoyuan, Taiwan.

Department of Obstetrics and Gynecology, Chang Gung Memorial Hospital, Linkou Medical Center and Chang Gung University College of Medicine, Kwei-Shan, Taoyuan, Taiwan.

出版信息

Taiwan J Obstet Gynecol. 2014 Sep;53(3):397-400. doi: 10.1016/j.tjog.2013.02.005.

Abstract

OBJECTIVE

A twin pregnancy consisting of a complete hydatidiform mole with a coexisting normal fetus is extremely rare with an incidence of 1/22,000 to 1/100,000. The incidence of preterm delivery is high and few pregnancies reach near term with a viable fetus.

CASE REPORT

A 34-year-old woman presented at 20 weeks of gestation with increased levels of serum beta human chorionic gonadotropin (beta-HCG) at 4.74 multiples of the median (310277.7 mIU/mL). Ultrasonography showed a hydatidiform mole together with a normal fetus. Fetal karyotyping revealed 46XY. The serum beta-HCG levels were followed up throughout the remainder of the pregnancy. A male infant weighting 2260 g and the molar tissue were delivered at 37 weeks of gestation. The karyotype of the molar tissue showed 46XX and the histopathological report confirmed our diagnosis. At 4 months postpartum, metastatic gestational trophoblastic disease of the lung was diagnosed in the mother by a computed tomography scan due to increased beta-HCG levels. The patient received three unsuccessful cycles of methotrexate and folinate. Another four cycles of chemotherapy consisting of etoposide, methotrexate, actinomycin D, cyclophosphamide, and vincristine (EMA-CO) were initiated and the beta-HCG levels returned to normal. There was no evidence of recurrence in the subsequent 5 years of regular follow up.

CONCLUSION

A pregnancy with a complete hydatidiform mole and a living cotwin can be a serious threat to the health of both the mother and the fetus. Early diagnosis depends on a combination of detecting an unusually high level of serum beta-HCG and ultrasound examination. We suggest that continuation of the pregnancy may be an acceptable option and that the pregnancy may continue until term if a normal fetal anatomy is assured and maternal complications are under control. Patients require careful postpartum follow up and any recurrent disease should be managed aggressively.

摘要

目的

一个双胎妊娠中,一个为完全性葡萄胎且并存一个正常胎儿的情况极为罕见,发生率为1/22,000至1/100,000。早产发生率很高,很少有妊娠能接近足月并娩出存活胎儿。

病例报告

一名34岁女性在妊娠20周时就诊,血清β-人绒毛膜促性腺激素(β-HCG)水平升高至中位数的4.74倍(310277.7 mIU/mL)。超声检查显示一个葡萄胎和一个正常胎儿。胎儿核型分析显示为46,XY。在整个孕期剩余时间对血清β-HCG水平进行了随访。在妊娠37周时娩出一名体重2260 g的男婴和葡萄胎组织。葡萄胎组织的核型显示为46,XX,组织病理学报告证实了我们的诊断。产后4个月,由于β-HCG水平升高,通过计算机断层扫描在母亲中诊断出肺部转移性妊娠滋养细胞疾病。患者接受了三个周期的甲氨蝶呤和亚叶酸治疗,但未成功。随后开始了另外四个周期由依托泊苷、甲氨蝶呤、放线菌素D、环磷酰胺和长春新碱组成的化疗(EMA-CO),β-HCG水平恢复正常。在随后5年的定期随访中没有复发迹象。

结论

一个伴有完全性葡萄胎和一个存活的双胎之一的妊娠可能对母亲和胎儿的健康构成严重威胁。早期诊断依赖于检测血清β-HCG异常高水平和超声检查相结合。我们建议继续妊娠可能是一个可接受的选择,并且如果能确保胎儿解剖结构正常且母体并发症得到控制,妊娠可以持续至足月。患者需要产后仔细随访,任何复发性疾病都应积极处理。

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