Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan; Department of Biotechnology, Asia University, Taichung, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang-Ming University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang-Ming University, Taipei, Taiwan.
Genephile Bioscience Laboratory, Ko's Obstetrics and Gynecology, Taipei, Taiwan.
Taiwan J Obstet Gynecol. 2014 Dec;53(4):572-8. doi: 10.1016/j.tjog.2014.10.001.
To present first-trimester molecular diagnosis of complete hydatidiform mole (CHM) associated with dizygotic twin pregnancy conceived by intrauterine insemination.
A 32-year-old woman presented to the hospital with a huge complex cystic mass measuring about 8.5 cm × 4.1 cm in the uterine cavity and a living co-existing fetus with fetal biometry equivalent to 9 weeks. She underwent chorionic villus sampling at 13 weeks of gestation, and microsatellite genotyping for molar pregnancy test was applied. A molar pregnancy test was performed by a short tandem repeat (STR) identifier polymerase chain reaction (PCR) polymorphic marker analysis. The pregnancy was terminated at 14 weeks of gestation. Postnatal polymorphic DNA marker analysis of the placenta by quantitative fluorescent PCR (QF-PCR) was performed. Analysis of maternal blood total β-human chorionic gonadotropin revealed a high level of 551,600 mIU/mL at 10 weeks of gestation and a level of 1.0 mIU/mL at 15 weeks postpartum. The woman was doing well at 4 months after delivery.
The results of STR identifier PCR polymorphic marker analysis showed androgenic conception in the complex cystic mass and biparental conception in the living fetus. Pathological analysis of the cystic mass confirmed the diagnosis of CHM. The results of QF-PCR showed biparental inheritance in the normal fetus and complete paternal homozygosity in the CHM of the abnormal fetus in all STRs, indicating dizygotic twinning and CHM of monospermy.
Prenatal sonographic diagnosis of placentomegaly with many grape-like vesicles should include a differential diagnosis of CHM, partial hydatidiform mole (PHM), placental mesenchymal dysplasia (PMD), and recurrent hydatidiform mole. Microsatellite genotyping for molar pregnancy testing and zygosity testing is useful in cases of prenatal diagnosis of placentomegaly associated with many grape-like vesicles and a twin pregnancy with a living fetus in the first trimester.
介绍首例通过宫腔内授精受孕的二倍体双胞胎妊娠的完全性葡萄胎(CHM)的早孕期分子诊断。
一位 32 岁的女性因宫腔内 8.5cm×4.1cm 的巨大复杂囊性肿块和共存的活胎就诊,胎儿生物测量相当于 9 周。她在妊娠 13 周时进行了绒毛膜绒毛取样,并进行了葡萄胎试验的微卫星基因分型。通过短串联重复(STR)标识符聚合酶链反应(PCR)多态性标记分析进行了葡萄胎试验。在妊娠 14 周时终止了妊娠。通过定量荧光 PCR(QF-PCR)对胎盘产后多态性 DNA 标记进行了分析。在妊娠 10 周时,母体血总β-人绒毛膜促性腺激素水平为 551600mIU/mL,在产后 15 周时为 1.0mIU/mL。该女性在产后 4 个月时情况良好。
STR 标识符 PCR 多态性标记分析结果显示,复杂囊性肿块为雄性妊娠,活胎为双亲妊娠。囊性肿块的病理分析证实了 CHM 的诊断。QF-PCR 结果显示,在所有 STR 中,正常胎儿为双亲遗传,异常胎儿的 CHM 为完全父系纯合子,提示为二倍体双胞胎和单精受精的 CHM。
早孕期超声诊断胎盘肿大伴多发葡萄状囊泡时,应包括 CHM、部分性葡萄胎(PHM)、胎盘间质发育不良(PMD)和复发性葡萄胎的鉴别诊断。在早孕期胎盘肿大伴多发葡萄状囊泡和双胎妊娠且有活胎的情况下,微卫星基因分型进行葡萄胎试验和二倍体检测有助于产前诊断。