First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination

被引:4
作者
Chen, Chih-Ping [1 ,2 ,3 ,4 ,5 ,6 ]
Ko, Tsang-Ming [7 ]
Chen, Chen-Yu [1 ]
Wang, Tao-Yeuan [8 ,9 ,10 ]
Chern, Schu-Rern [2 ]
Kuo, Yu-Ling [11 ]
Wang, Wayseen [2 ,12 ]
机构
[1] Mackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[2] Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan
[3] Asia Univ, Dept Biotechnol, Taichung, Taiwan
[4] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung, Taiwan
[5] Natl Yang Ming Univ, Inst Clin & Community Hlth Nursing, Taipei 112, Taiwan
[6] Natl Yang Ming Univ, Sch Med, Dept Obstet & Gynecol, Taipei 112, Taiwan
[7] Kos Obstet & Gynecol, Genephile Biosci Lab, Taipei, Taiwan
[8] Mackay Mem Hosp, Dept Pathol, Taipei, Taiwan
[9] Mackay Med Coll, Dept Med, New Taipei City, Taiwan
[10] Mackay Jr Coll Med Nursing & Management, Taipei, Taiwan
[11] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Obstet & Gynecol, Kaohsiung, Taiwan
[12] Tatung Univ, Dept Bioengn, Taipei 104, Taiwan
来源
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | 2014年 / 53卷 / 04期
关键词
complete hydatidiform mole; dizygotic twin; intrauterine insemination; microsatellite genotyping; prenatal diagnosis; PLACENTAL MESENCHYMAL DYSPLASIA; COEXISTENT FETUS; ANDROGENETIC/BIPARENTAL MOSAICISM; GENETIC-ANALYSIS; MUTATIONS; UTILITY; ORIGIN; IDENTIFICATION; ROUTINE; FETAL;
D O I
10.1016/j.tjog.2014.10.001
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To present first-trimester molecular diagnosis of complete hydatidiform mole (CHM) associated with dizygotic twin pregnancy conceived by intrauterine insemination. Materials and methods: A 32-year-old woman presented to the hospital with a huge complex cystic mass measuring about 8.5 cm x 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 beta-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. Results: 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. Conclusion: 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. Copyright (C) 2014, Taiwan Association of Obstetrics & Gynecology. Published by Elsevier Taiwan LLC. All rights reserved.
引用
收藏
页码:572 / 578
页数:7
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