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三倍父源贡献至一个正常/完全性葡萄胎嵌合单胎胎盘。

Triple paternal contribution to a normal/complete molar chimeric singleton placenta.

作者信息

Ariel I, Goldman-Wohl D, Yagel S, Gazit E, Loewenthal R

机构信息

The Perinatal Pathology Unit, Department of Pathology, Hadassah-Hebrew University Medical Center, Mount Scopus, PO Box 24035, Jerusalem il-91240, Israel.

The Magda and Richard Hoffman Center for Human Placenta Research, Department of Obstetrics and Gynecology, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem, Israel.

出版信息

Hum Reprod. 2017 May 1;32(5):993-998. doi: 10.1093/humrep/dex053.

Abstract

A comprehensive study of unusual cases of placental pathology may provide insight into mechanisms of normal human fertilization and early embryonic development by examining the exception to the rule. A gravida three para two 39-year-old woman was monitored by ultrasound from 16 weeks of gestation for cystic placenta. A female newborn was born at 36 weeks gestation. Pathologic examination of the partially cystic placenta revealed a singleton placenta comprised of 2/3 normal placenta and 1/3 complete hydatidiform mole, largely degenerated. Immunostaining for p57 was negative in stromal cells of the molar villi. Chromogenic in-situ hybridization revealed diploidy in both normal and molar parts. A total of 16 microsatellites were studied by short tandem repeat analysis, 11 of which were informative. The analysis revealed bipaternal molar tissue of dispermic origin. The paternal monospermic contribution to the normal part was different from that in the molar part, thus resulting in tripaternal contribution to the conceptus. A chimera is a single organism composed of two or more different populations of genetically distinct cells that originated from different zygotes (tetragametic) whereas mosaic is a mixture of two cell lines in one organism originating from one zygote. The possible mechanisms leading to the formation of chimeric/mosaic placenta in our case (one of the components being complete hydatidiform mole), including twinning, fusion at an early embryonic stage and diploidization of triploids, are discussed.

摘要

对胎盘病理学异常病例进行全面研究,通过审视规则的例外情况,可能会为人类正常受精和早期胚胎发育机制提供见解。一名39岁、孕3产2的孕妇从妊娠16周起接受超声监测,以检查是否有胎盘囊肿。妊娠36周时娩出一名女婴。对部分呈囊性的胎盘进行病理检查发现,这是一个单胎胎盘,其中2/3为正常胎盘,1/3为完全性葡萄胎,且大部分已退化。葡萄状绒毛间质细胞的p57免疫染色呈阴性。显色原位杂交显示正常部分和葡萄胎部分均为二倍体。通过短串联重复序列分析研究了总共16个微卫星,其中11个具有信息价值。分析显示,葡萄胎组织起源于双精子受精的双父系。父系单精子对正常部分的贡献与对葡萄胎部分的不同,从而导致对胎儿的三父系贡献。嵌合体是指由两种或更多种遗传上不同的细胞群体组成的单一生物体,这些细胞群体源自不同的受精卵(四配子体),而镶嵌体是指在一个生物体中由源自一个受精卵的两种细胞系组成的混合物。本文讨论了导致我们病例中形成嵌合/镶嵌胎盘(其中一个组成部分为完全性葡萄胎)的可能机制,包括双胎妊娠、早期胚胎阶段的融合以及三倍体二倍体化。

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