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经导管封堵合并右位三房心的双房间隔缺损时的一种罕见并发症:病例报告

A Rare Complication During Transcatheter Closure of Double Atrial Septal Defects With Incomplete Cor Triatriatum Dexter: A Case Report.

作者信息

Chen Ping-Hong, Liu Yi-Ching, Dai Zen-Kong, Chen I-Chen, Lo Shih-Hsing, Wu Jiunn-Ren, Wu Yen-Hsien, Hsu Jong-Hau

机构信息

Department of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.

Department of Pediatrics, E-Da Hospital/I-Shou University, Kaohsiung, Taiwan.

出版信息

Front Cardiovasc Med. 2022 Feb 24;8:815312. doi: 10.3389/fcvm.2021.815312. eCollection 2021.

DOI:10.3389/fcvm.2021.815312
PMID:35284495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8907262/
Abstract

The cor triatiatum dexter is an embryologic remnant derived from the right atrium and totally separate from the right atrium. An incomplete cor triatiatum dexter (iCTD) means a partially obstructive remnant at the right atrium. It is usually formed by a remnant of the Eustachian valve (EV), Thebesian valve (ThV), or Chiari network (CN). This anatomic variant is usually asymptomatic but is often associated with other heart abnormalities including atrial septal defects (ASDs), and has the potential to hamper percutaneous heart procedures such as electrophysiological study or ASD closure. Herein, we report a rare complication, transient heart ischemia, in transcatheter closure of double ASDs in a 55-year-old woman with EV. This rare complication was thought to be caused by coronary sinus obstruction during device placement. The ischemic change was resolved spontaneously after we withdrew the device. For a second attempt, we adjusted the position of the device to avoid coronary sinus obstruction under transesophageal echocardiogram guidance and the device was smoothly deployed in a good position with a minimal residual shunt. This case suggests that anatomy details in percutaneous heart procedures are important, and this rare and dangerous complication, heart ischemia, should be identified immediately during the procedure.

摘要

右三房心是一种源于右心房的胚胎残余结构,与右心房完全分隔。不完全性右三房心(iCTD)指右心房处部分梗阻性的残余结构。它通常由欧氏瓣(EV)、心最小静脉瓣(ThV)或希阿里网(CN)的残余部分形成。这种解剖变异通常无症状,但常与包括房间隔缺损(ASD)在内的其他心脏异常相关,并且有可能妨碍诸如电生理研究或ASD封堵等经皮心脏操作。在此,我们报告了一例55岁患有欧氏瓣的女性在经导管封堵双ASD过程中出现的罕见并发症——短暂性心脏缺血。这种罕见并发症被认为是由于装置放置过程中冠状窦梗阻所致。在我们撤出装置后,缺血改变自行缓解。第二次尝试时,我们在经食管超声心动图引导下调整装置位置以避免冠状窦梗阻,装置顺利放置于良好位置,残余分流极小。该病例提示,经皮心脏操作中的解剖细节很重要,并且这种罕见且危险的并发症——心脏缺血,在操作过程中应立即识别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffc/8907262/33afef24ea58/fcvm-08-815312-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffc/8907262/500c426fe937/fcvm-08-815312-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffc/8907262/d438d8a5231a/fcvm-08-815312-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffc/8907262/0c2c670a9bba/fcvm-08-815312-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffc/8907262/33afef24ea58/fcvm-08-815312-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffc/8907262/500c426fe937/fcvm-08-815312-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffc/8907262/d438d8a5231a/fcvm-08-815312-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffc/8907262/0c2c670a9bba/fcvm-08-815312-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffc/8907262/33afef24ea58/fcvm-08-815312-g0004.jpg

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2
Bands in the Heart: Multimodality Imaging Review.心中的旋律:多模态影像综述。
Radiographics. 2019 Sep-Oct;39(5):1238-1263. doi: 10.1148/rg.2019180176. Epub 2019 Aug 2.
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Incomplete Cor Triatriatum Dexter: An Unsettling Guest in the Percutaneous Closure of Atrial Septal Defects.
Rev Esp Cardiol (Engl Ed). 2019 Jul;72(7):582-583. doi: 10.1016/j.rec.2018.05.036. Epub 2018 Aug 13.
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Eustachian valve-Masquerading ASD rim.咽鼓管瓣膜——伪装成房间隔缺损边缘。
Indian Heart J. 2017 May-Jun;69(3):422-423. doi: 10.1016/j.ihj.2017.04.011. Epub 2017 Apr 26.
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The importance of recognizing the prominent Eustachian valve in the evaluation of atrial septal defects before percutaneous or surgical closure.在经皮或手术闭合房间隔缺损之前的评估中,认识到明显的咽鼓管瓣的重要性。
Indian Heart J. 2017 May-Jun;69(3):355-356. doi: 10.1016/j.ihj.2017.04.018. Epub 2017 May 12.
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The Presence of a Large Chiari Network in a Patient with Atrial Fibrillation and Stroke.一名患有心房颤动和中风的患者体内存在大型奇阿里网。
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