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足月分娩的双绒毛膜双胎妊娠合并三道剖宫产瘢痕产妇:病例报告

Woman with term presentation of acaridac twin pregnancy with three cesarean section scars: a case report.

作者信息

Dinsa Leta Hinkosa, Hailu Alemu Merga, Eticha Amenu Diriba

机构信息

Department of Midwifery, Inistitiute of health Sciences,Wolegga University, Nekemte City, Oromia Regional state, Ethiopia.

Department Obstetrics and Gynecology, Inistitiute of Health Science,Wolegga University, Nekemte City, Oromia Regional state, Ethiopia.

出版信息

J Med Case Rep. 2025 Jul 25;19(1):367. doi: 10.1186/s13256-025-05168-4.

Abstract

BACKGROUND

Twin reversed arterial perfusion sequence is the most severe and specific complication in monochorionic twin pregnancies, described by vascular anastomosis and partial or complete lack of cardiac development in one twin.

OBJECTIVE

This report aims to present a unique discussion on cardiac twin pregnancy in an acardiac setting. In this acardiac twin pregnancy, one twin has no upper body part including the heart while the other twin (pump twin) has normal morphology. Acardiac twin pregnancy rarely reaches term, and the pump twin survives. Therefore, expectant management with close antenatal care follow-up can have good prognosis. We present a case of acardiac twin pregnancy. A 31-year-old G-IV P-III mother was referred to Wolegga University Teaching Referral Hospital for antenatal care service at gestational age of 24 weeks + 3 days from reliable last normal menstrual period. She is of Black African ethnicity, and on her first contact, twin intrauterine pregnancy with an acardiac twin was diagnosed. Then, expectant management was decided, and the pregnancy was closely monitored until term. At 38 weeks of gestation, an elective cesarean section was done. The acardiac twin died right away after the cord was clamped, while the pump twin is healthy and currently in follow-up.

CONCLUSION

Acardiac twin pregnancy rarely reaches term. To take prompt and appropriate measures, antenatal diagnosis of twin reversed arterial perfusion sequence is crucial.

摘要

背景

双胎反向动脉灌注序列征是单绒毛膜双胎妊娠中最严重且最具特异性的并发症,其特征为血管吻合以及一个胎儿部分或完全缺乏心脏发育。

目的

本报告旨在对无心畸形情况下的双胎妊娠进行独特探讨。在这种无心畸形双胎妊娠中,一个胎儿没有包括心脏在内的上半身部分,而另一个胎儿(供血胎儿)形态正常。无心畸形双胎妊娠很少能足月,供血胎儿存活。因此,通过密切的产前检查进行期待治疗可获得良好预后。我们报告一例无心畸形双胎妊娠病例。一名31岁、孕4产3的母亲,根据可靠的末次正常月经日期,在孕24周+3天时被转诊至沃莱加大学教学转诊医院接受产前检查。她是非洲黑人种族,初次就诊时被诊断为双胎宫内妊娠,其中一个为无心畸形胎儿。随后决定进行期待治疗,并对妊娠进行密切监测直至足月。孕38周时,进行了择期剖宫产。无心畸形胎儿在脐带结扎后立即死亡,而供血胎儿健康,目前正在接受随访。

结论

无心畸形双胎妊娠很少能足月。为及时采取适当措施,产前诊断双胎反向动脉灌注序列征至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19c9/12297647/355d9478fec6/13256_2025_5168_Fig1_HTML.jpg

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