Bohec Caroline, Douet-Guilbert Nathalie, Basinko Audrey, Le Bris Marie-Josée, Marcorelles Pascale, Audrézet Marie-Pierre, Tetefort Rémi, Bages Karine, Collet Michel, Morel Frederic, De Braekeleer Marc
Department of Gynecology, Obstetrics and Reproductive Medicine, Centre Hospitalier Universitaire Brest, Brest, France.
Fetal Pediatr Pathol. 2010;29(6):424-30. doi: 10.3109/15513815.2010.505630.
We report twins for whom ultrasound examinations revealed a Turner syndrome in the female fetus and a normal male fetus. A selective pregnancy termination was decided on the female fetus with hydrops. The death of both twins called in question the chorionic diagnosis. Amniotic fluid cytogenetic analysis revealed a 45,X karyotype in the female twin and a 47,XYY karyotype in the male twin. Molecular cytogenetic analysis on genital and renal cells showed different levels of 45,X/47,XYY mosaicism in both twins; molecular analysis on the amniocytes showed monozygosity. Monozygotic twins with discordant sex are very rare. This study showed the difficult diagnosis and management of a monochorionic twin pregnancy with discordant fetal sex.
我们报告了一对双胞胎,超声检查显示女性胎儿为特纳综合征,男性胎儿正常。对患有水肿的女性胎儿决定进行选择性终止妊娠。双胞胎均死亡,这使绒毛膜诊断受到质疑。羊水细胞遗传学分析显示,女性双胞胎的核型为45,X,男性双胞胎的核型为47,XYY。对生殖器官和肾脏细胞进行的分子细胞遗传学分析显示,两个双胞胎中均存在不同程度的45,X/47,XYY嵌合体;对羊水细胞的分子分析显示为单合子性。性别不一致的单卵双胞胎非常罕见。本研究显示了单绒毛膜双胎妊娠且胎儿性别不一致时诊断和处理的困难。