The first reported case of double trisomy 10 and 20 in a product of conception.

Joshua Fernandez De La Vega, Arian Pourmehdi Lahiji, Caitlin Raymond, Song Han, Harshwardhan Thaker, Jianli Dong
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Abstract

Background: Double trisomies are rare findings among products of conception and are often lethal to the developing embryo or fetus.

Methods: Here we describe a double trisomy case with symptoms of threatened miscarriage at 9 weeks gestation. Ultrasound revealed an anembryonic pregnancy. Pregnancy was terminated by dilation and curettage at gestational age 11 weeks and 6 days. Histologic examination and chromosome microarray were performed on a formalin-fixed product of conception (POC) sample to identify the cause of the anembryonic pregnancy.

Results: Chromosome microarray analysis revealed a female chromosome complement with double trisomies 10 and 20, arr(10,20)x3, consistent with a karyotype of 48,XX,+10,+20.

Conclusion: To the best of our knowledge, this is the first reported case of double trisomy 10 and 20 in a POC. Due to nonspecific histopathological findings, chromosomal microarray is a powerful tool in identifying and differentiating chromosomal aneuploidies.

首例报告的 10 和 20 双三体受孕病例。
背景:方法:本文描述了一个双三体综合征病例,患者在妊娠 9 周时出现流产症状。超声波显示为无胚胎妊娠。在妊娠 11 周零 6 天时,通过扩张和刮宫术终止了妊娠。对福尔马林固定的受孕产物(POC)样本进行了组织学检查和染色体微阵列分析,以确定无胚胎妊娠的原因:结果:染色体微阵列分析显示,女性染色体补体为10和20双三体,即arr(10,20)x3,核型为48,XX,+10,+20:据我们所知,这是首例在 POC 中发现 10 和 20 双三体的病例。由于组织病理学发现的非特异性,染色体微阵列是鉴别和区分染色体非整倍体的有力工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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