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Twin pregnancy with a complete hydatidiform mole and surviving co-existent fetus.双胎妊娠,其中一胎为完全性葡萄胎,另一存活胎儿并存。
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A complete hydatidiform mole and coexisting viable fetus in a twin pregnancy: a case report with literature review.完全性葡萄胎并同时存在存活胎儿的双胎妊娠:病例报告并文献复习
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Term delivery of a complete hydatidiform mole with a coexisting living fetus followed by successful treatment of maternal metastatic gestational trophoblastic disease.足月分娩完全性葡萄胎并伴有存活胎儿,随后成功治疗母体转移性妊娠滋养细胞疾病。
Taiwan J Obstet Gynecol. 2014 Sep;53(3):397-400. doi: 10.1016/j.tjog.2013.02.005.

引用本文的文献

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Complete Hydatidiform Mole with Twin Live Fetuses in a Triplet Pregnancy: A Case Report and Literature Review.三胎妊娠中完全性葡萄胎合并双活胎:一例报告及文献复习
Int J Womens Health. 2024 Oct 23;16:1701-1713. doi: 10.2147/IJWH.S484634. eCollection 2024.
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Twin Gestation with Complete Hydatidiform Mole and Demise of Co-Existing Fetus.双胎妊娠合并完全性葡萄胎及并存胎儿死亡
Sultan Qaboos Univ Med J. 2022 Aug;22(3):430-431. doi: 10.18295/squmj.9.2021.132. Epub 2022 Aug 25.

本文引用的文献

1
A challenging case of twin pregnancy with complete hydatidiform mole and co-existing normal live fetus - A case report and review of the literature.一例伴有完全性葡萄胎和并存正常活胎的双胎妊娠疑难病例——病例报告及文献复习
Gynecol Oncol Rep. 2019 Dec 5;31:100519. doi: 10.1016/j.gore.2019.100519. eCollection 2020 Feb.
2
Perinatal outcome of pregnancies complicated by placental chorioangioma: systematic review and meta-analysis.合并胎盘绒毛膜血管瘤的妊娠的围产期结局:系统评价和荟萃分析
Ultrasound Obstet Gynecol. 2020 Apr;55(4):441-449. doi: 10.1002/uog.20304.
3
Prenatal diagnosis of multiple large subchorionic placental cysts with intracystic hemorraghe.产前诊断多发性大的绒毛膜下胎盘囊肿伴囊内出血。
Facts Views Vis Obgyn. 2017 Dec;9(4):223-225.
4
Complete hydatidiform mole with co-existing fetus: Predictors of live birth.完全性葡萄胎合并存活胎儿:活产的预测因素。
Eur J Obstet Gynecol Reprod Biol. 2017 May;212:1-8. doi: 10.1016/j.ejogrb.2017.03.013. Epub 2017 Mar 7.
5
Multiple pregnancies with complete mole and coexisting normal fetus in North and South America: A retrospective multicenter cohort and literature review.北美和南美完全性葡萄胎伴共存正常胎儿的多胎妊娠:回顾性多中心队列研究和文献复习。
Gynecol Oncol. 2017 Apr;145(1):88-95. doi: 10.1016/j.ygyno.2017.01.021. Epub 2017 Jan 26.
6
Viable triplet pregnancy coexisting with a complete molar pregnancy.存活的三胎妊娠合并完全性葡萄胎。
Clin Case Rep. 2016 Jan 20;4(3):247-9. doi: 10.1002/ccr3.417. eCollection 2016 Mar.
7
Term delivery of a complete hydatidiform mole with a coexisting living fetus followed by successful treatment of maternal metastatic gestational trophoblastic disease.足月分娩完全性葡萄胎并伴有存活胎儿,随后成功治疗母体转移性妊娠滋养细胞疾病。
Taiwan J Obstet Gynecol. 2014 Sep;53(3):397-400. doi: 10.1016/j.tjog.2013.02.005.
8
Placental mesenchymal dysplasia.胎盘间充质发育不良。
Am J Obstet Gynecol. 2011 Dec;205(6):e3-5. doi: 10.1016/j.ajog.2011.08.019. Epub 2011 Aug 22.
9
Placental mesenchymal dysplasia presenting as a twin gestation with complete molar pregnancy.胎盘间叶发育不良表现为双胎妊娠合并完全性葡萄胎。
Obstet Gynecol. 2011 Aug;118(2 Pt 2):445-449. doi: 10.1097/AOG.0b013e3182161828.
10
Prenatal diagnosis and management of twin pregnancies complicated by a co-existing molar pregnancy.双胎妊娠合并葡萄胎的产前诊断与管理
Prenat Diagn. 2005 Sep;25(9):772-6. doi: 10.1002/pd.1272.

三胞胎中偶然诊断出胎儿哀伤综合征。

Incidental diagnosis of sad fetus syndrome in triplets.

机构信息

Obstetrics and Gynecology, All India Institute of Medical Sciences, New Delhi, Delhi, India.

Obstetrics and Gynecology, All India Institute of Medical Sciences, New Delhi, Delhi, India

出版信息

BMJ Case Rep. 2021 Feb 4;14(2):e238977. doi: 10.1136/bcr-2020-238977.

DOI:10.1136/bcr-2020-238977
PMID:33541990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7868267/
Abstract

An unusual presentation of gestational trophoblastic disease is twin molar pregnancy, rarest in triplets with differentials being partial/complete mole, placental mesenchymal dysplasia (PMD), placental cysts or chorioangioma each with different complications. Counselling to continue pregnancy depends on diagnosis. A 37-year-old GPL, donor oocyte In vitro fertlisation (IVF) twin pregnancy was referred at 24 weeks with cystic areas in placenta. Probability of twin partial mole or PMD was assessed. The scan of fetuses showed normal growth, no structural anomalies. Biochemical markers showed high maternal beta human chorionic gonadotropin (β-hCG). Amniocentesis of molar fetus revealed normal karyotype. Likely diagnosis made as twin partial mole. The patient delivered by caesarean section at 28 weeks due to preterm labour. Twins, a male and a female baby, were delivered with three placentas, two normal and the third with molar changes and no fetal parts. Diagnosis was revised as triplet with partial mole, which was confirmed on histopathology. Serial monitoring of β-hCG became undetectable by eighth week. The male baby died on day 4. The mother and the female baby were discharged.

摘要

葡萄胎妊娠的一种不常见表现为双胎葡萄胎妊娠,三胎中极罕见,鉴别诊断包括部分性/完全性葡萄胎、胎盘间质发育不良(PMD)、胎盘囊肿或绒毛膜血管瘤,每种疾病都有不同的并发症。继续妊娠的咨询取决于诊断。一位 37 岁的 GPL,供卵体外受精(IVF)双胎妊娠,在 24 周时因胎盘内囊性区域而被转诊。评估了双胎部分性葡萄胎或 PMD 的可能性。胎儿扫描显示正常生长,无结构异常。生化标志物显示母体β人绒毛膜促性腺激素(β-hCG)水平较高。对摩尔胎儿进行羊膜穿刺术显示正常核型。可能的诊断为双胎部分性葡萄胎。由于早产,孕妇在 28 周时行剖宫产分娩。分娩出一对龙凤胎,有三个胎盘,两个正常,第三个胎盘有葡萄胎样改变且无胎儿组织。诊断修订为三胎部分性葡萄胎,组织病理学检查证实了这一诊断。β-hCG 的连续监测在第八周时已无法检测到。男婴于第 4 天死亡。母亲和女婴已出院。