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一例罕见的双胎输血综合征合并受血儿双胎动脉导管过早收缩的病例。

An unusual case of twin anemia polycythemia sequence complicated by premature ductus arteriosus constriction of the recipient twin.

作者信息

Chokshi Ravi, McMullen Kathryn, Soni Shelly, Tunks Robert, O'Brien James

机构信息

Division of Maternal-Fetal Medicine, Penn State University Milton S. Hershey Medical Center, Penn State College of Medicine, Hershey, PA, USA.

Department of Obstetrics & Gynecology, Penn State University Milton S. Hershey Medical Center, Penn State College of Medicine, Hershey, PA, USA.

出版信息

Case Rep Perinat Med. 2024 Oct 21;13(1):20240027. doi: 10.1515/crpm-2024-0027. eCollection 2024 Jan.

Abstract

OBJECTIVES

To add to the nascent literature on twin anemia polycythemia sequence by presenting a unique cardiac complication in the recipient twin.

CASE PRESENTATION

We describe a monochorionic diamniotic pregnancy complicated by twin anemia polycythemia sequence wherein the recipient twin developed signs of right heart failure secondary to premature ductus arteriosus constriction, requiring iatrogenic preterm delivery to avoid intrauterine demise.

CONCLUSIONS

This case report introduces a previously undescribed complication of twin anemia polycythemia sequence and adds to the growing literature on this clinical entity.

摘要

目的

通过呈现受血儿独特的心脏并发症,补充关于双胎输血综合征的新兴文献。

病例报告

我们描述了一例单绒毛膜双羊膜囊妊娠合并双胎输血综合征,其中受血儿因动脉导管过早收缩出现右心衰竭体征,需要医源性早产以避免宫内死亡。

结论

本病例报告介绍了一种此前未被描述的双胎输血综合征并发症,并补充了关于这一临床实体的不断增加的文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6860/12048135/9f544f20ba2b/j_crpm-2024-0027_fig_001.jpg

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