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一例极为罕见的先天性肌束横跨右心房腔

An Extremely Rare Congenital Muscle Bundle Crossing the Right Atrial Cavity.

作者信息

Kofler Thomas, Wolfrum Mathias, Kobza Richard, Kretschmar Oliver, Toggweiler Stefan, Stämpfli Simon F

机构信息

Heart Center Lucerne, Luzerner Kantonsspital, Lucerne, Switzerland.

Pediatric Cardiology, Pediatric Heart Center, University Children's Hospital, Zurich, Switzerland.

出版信息

JACC Case Rep. 2022 Feb 2;4(3):128-132. doi: 10.1016/j.jaccas.2021.11.016.

DOI:10.1016/j.jaccas.2021.11.016
PMID:35199002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8853950/
Abstract

Muscle bundles in the right atrium are an extremely rare congenital anomaly. We report the case of a patient with 2 atrial septal defects and a large muscle bundle crossing the right atrium. Only 3 comparable cases have previously been published. ().

摘要

右心房肌束是一种极其罕见的先天性异常。我们报告了一例患有2个房间隔缺损和一条穿过右心房的大肌束的患者。此前仅发表过3例类似病例。()

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/475119e06220/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/74f63463f6e4/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/ba5712fc399a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/a48150210707/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/e76b81e2d10f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/828397629ac0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/475119e06220/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/74f63463f6e4/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/ba5712fc399a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/a48150210707/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/e76b81e2d10f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/828397629ac0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff6/8853950/475119e06220/gr5.jpg

相似文献

1
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本文引用的文献

1
Arrhythmias and conduction disorders associated with atrial septal defects.与房间隔缺损相关的心律失常和传导障碍。
J Thorac Dis. 2018 Sep;10(Suppl 24):S2940-S2944. doi: 10.21037/jtd.2018.08.27.
2
2018 AHA/ACC Guideline for the Management of Adults With Congenital Heart Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines.2018年美国心脏协会/美国心脏病学会成人先天性心脏病管理指南:美国心脏病学会/美国心脏协会临床实践指南工作组报告
J Am Coll Cardiol. 2019 Apr 2;73(12):e81-e192. doi: 10.1016/j.jacc.2018.08.1029. Epub 2018 Aug 16.
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Right Atrial Anomalous Muscle Bundle Presenting with Acute Superior Vena Cava Syndrome and Pulmonary Embolism: Surgical Management.
伴有急性上腔静脉综合征和肺栓塞的右心房异常肌束:外科治疗
Ann Vasc Surg. 2018 Oct;52:314.e17-314.e20. doi: 10.1016/j.avsg.2018.03.035. Epub 2018 May 22.
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Molecular and Cellular Mechanisms of Atrial Fibrosis in Atrial Fibrillation.心房颤动中心房纤维化的分子和细胞机制。
JACC Clin Electrophysiol. 2017 May;3(5):425-435. doi: 10.1016/j.jacep.2017.03.002. Epub 2017 May 15.
5
Incomplete Cor Triatriatum Dexter and Its Clinical and Technical Implications in Interatrial Shunt Device-Based Closure: An Intracardiac Echocardiography Study.
Congenit Heart Dis. 2016 Sep;11(5):420-425. doi: 10.1111/chd.12326. Epub 2016 Feb 17.
6
Atrial arrhythmias in adult patients with right- versus left-sided congenital heart disease anomalies.成人右心型先天性心脏病与左心型先天性心脏病患者的房性心律失常。
Am J Cardiol. 2010 Aug 15;106(4):547-51. doi: 10.1016/j.amjcard.2010.03.068.
7
The valve of the superior vena cava--the supernumerary structure of the precaval segment of the crista terminalis.上腔静脉瓣——界嵴前腔段的多余结构。
Folia Morphol (Warsz). 2007 Nov;66(4):303-6.
8
Congenital malformations of the right atrium and the coronary sinus: an analysis based on 103 cases reported in the literature and two additional cases.右心房及冠状窦先天性畸形:基于文献报道的103例及另外2例的分析
Chest. 2000 Jun;117(6):1740-8. doi: 10.1378/chest.117.6.1740.
9
Transcatheter closure of atrial septal defect and patent foramen ovale with ASDOS device (a multi-institutional European trial).
Am J Cardiol. 1998 Dec 1;82(11):1405-13. doi: 10.1016/s0002-9149(98)00650-x.
10
An anomalous muscle bundle inside the right atrium possibly related to the right venous valve.右心房内一条异常肌束,可能与右静脉瓣有关。
J Heart Valve Dis. 1997 Jul;6(4):439-40.