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法洛四联症矫正术后肺动脉瓣置入引发的右心室憩室:一例报告

Right ventricular diverticulum following a pulmonary valve placement for correction of tetralogy of Fallot: A case report.

作者信息

Martinez Juarez David, Gomez Monterrosas Omar, Tlecuitl Mendoza Alonso, Zamora Rosales Francisco, Álvarez Calderón Rodrigo, Cepeda Ortiz Daniel A, Espinosa Solis Erick E

机构信息

Department of Radiology, Christus Muguerza Hospital Betania, Puebla 72501, Mexico.

Department of Cardiology, Christus Muguerza Hospital Betania, Puebla 72501, Mexico.

出版信息

World J Cardiol. 2024 Dec 26;16(12):760-767. doi: 10.4330/wjc.v16.i12.760.

DOI:10.4330/wjc.v16.i12.760
PMID:39734813
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11669970/
Abstract

BACKGROUND

Ventricular diverticula are a rare congenital cardiac disorder presenting with an extremely low incidence. The presence of an apical diverticulum of the right ventricle has been associated with other congenital heart diseases such as tetralogy of Fallot. An important defining characteristic of ventricular diverticula that separates them from aneurysms through imaging techniques, is that they possess myocardial contraction synchronous to the adjacent walls, contributing to the ventricular stroke volume, so they do not usually require surgical treatment.

CASE SUMMARY

A 15-year-old male, currently asymptomatic, in follow up due to a pulmonary valve prosthesis placement and a history of corrected tetralogy of Fallot at 18 months old, underwent a cardiac magnetic resonance imaging in February 2024. A diverticulum was detected in the apical inferolateral wall of the right ventricle, which was not documented in the cardiac magnetic resonance imaging prior to valve prosthesis placement.

CONCLUSION

Right ventricular diverticula are a rare entity. To this date we could not find another case of a pulmonary valve placement, followed by a right ventricular diverticulum appearance.

摘要

背景

心室憩室是一种罕见的先天性心脏疾病,发病率极低。右心室心尖部憩室的存在与其他先天性心脏病如法洛四联症有关。通过成像技术将心室憩室与动脉瘤区分开来的一个重要特征是,它们具有与相邻心肌壁同步的收缩,有助于心室的每搏输出量,因此通常不需要手术治疗。

病例摘要

一名15岁男性,目前无症状,因曾接受肺动脉瓣置换术且18个月大时曾接受法洛四联症矫正手术而接受随访,于2024年2月接受了心脏磁共振成像检查。在右心室心尖下外侧壁发现一个憩室,在瓣膜置换术前的心脏磁共振成像中未记录到该憩室。

结论

右心室憩室是一种罕见的病症。截至目前,我们尚未发现另一例肺动脉瓣置换术后出现右心室憩室的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/a5bdff1a72da/WJC-16-760-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/6f7e2ce37c17/WJC-16-760-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/e58d81cb4fd2/WJC-16-760-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/9d8bda82a536/WJC-16-760-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/90e3d1a6cbf9/WJC-16-760-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/24c611ae2fe9/WJC-16-760-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/a5bdff1a72da/WJC-16-760-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/6f7e2ce37c17/WJC-16-760-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/e58d81cb4fd2/WJC-16-760-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/9d8bda82a536/WJC-16-760-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/90e3d1a6cbf9/WJC-16-760-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/24c611ae2fe9/WJC-16-760-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b76/11669970/a5bdff1a72da/WJC-16-760-g006.jpg

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本文引用的文献

1
Congenital right ventricular diverticulum: An atypical presentation.先天性右心室憩室:一种非典型表现。
Ann Pediatr Cardiol. 2020 Oct-Dec;13(4):368-370. doi: 10.4103/apc.APC_49_20. Epub 2020 Jul 24.
2
True Right Ventricular Diverticulum in Tetralogy of Fallot: A Rare Association.法洛四联症中的真性右心室憩室:一种罕见的关联。
Ann Thorac Surg. 2019 Nov;108(5):e345. doi: 10.1016/j.athoracsur.2019.04.056. Epub 2019 Jun 8.
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Current outcomes and treatment of tetralogy of Fallot.法洛四联症的当前治疗结果与治疗方法
F1000Res. 2019 Aug 29;8. doi: 10.12688/f1000research.17174.1. eCollection 2019.
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Eur Heart J Case Rep. 2019 Jun 1;3(2). doi: 10.1093/ehjcr/ytz081.
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Percutaneous closure of a prosthetic pulmonary paravalvular leak.经皮封堵人工肺瓣周漏
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True diverticulum of the right ventricle: two cases associated with tetralogy of Fallot.
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