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心脏移植治疗罕见错构瘤所致室性心律失常

Heart transplantation for ventricular arrhythmia caused by a rare hamartoma.

机构信息

Division of Cardiovascular Surgery, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.

出版信息

J Heart Lung Transplant. 2009 Oct;28(10):1114-5. doi: 10.1016/j.healun.2009.06.015.

DOI:10.1016/j.healun.2009.06.015
PMID:19782298
Abstract

Hamartoma of mature cardiac myocytes is a form of cardiac tumor that shares some features with hypertrophic cardiomyopathy and rhabdomyomas. Here we describe a patient with a ventricular hamartoma complicated with ventricular tachycardia. Resection was not practical because of difficulty in maintaining the ventricular geometry, so heart transplantation was done.

摘要

成熟心肌细胞的错构瘤是一种心脏肿瘤,与肥厚型心肌病和横纹肌瘤有一些共同特征。在此,我们描述了一例伴有室性心动过速的心室错构瘤患者。由于难以维持心室几何形状,切除并不实用,因此进行了心脏移植。

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Heart transplantation for ventricular arrhythmia caused by a rare hamartoma.心脏移植治疗罕见错构瘤所致室性心律失常
J Heart Lung Transplant. 2009 Oct;28(10):1114-5. doi: 10.1016/j.healun.2009.06.015.
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引用本文的文献

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Hamartoma of mature cardiomyocytes presenting with atypical angina, F-fluorodeoxyglucose positron emission tomography uptake, and myocardial bridging: a case report.成熟心肌细胞错构瘤伴非典型心绞痛、F-氟脱氧葡萄糖正电子发射断层扫描摄取及心肌桥:病例报告
Eur Heart J Case Rep. 2023 Feb 14;7(3):ytad077. doi: 10.1093/ehjcr/ytad077. eCollection 2023 Mar.
2
Atypical Presentation of Right Ventricular Cardiac Hamartoma in a Young Man.年轻男性右心室血管平滑肌脂肪瘤的非典型表现。
Methodist Debakey Cardiovasc J. 2022 Oct 4;18(1):102-107. doi: 10.14797/mdcvj.1158. eCollection 2022.
3
A Case of Ventricular Tachycardia Caused by a Rare Cardiac Mesenchymal Hamartoma.
一例由罕见的心脏间叶性错构瘤引起的室性心动过速病例。
JACC Case Rep. 2020 Jun 17;2(7):1049-1055. doi: 10.1016/j.jaccas.2020.04.038.
4
Mature cardiac myocytohamartoma: a case report and review of literature.成熟性心脏肌细胞错构瘤:一例病例报告并文献复习
Int J Clin Exp Pathol. 2019 Apr 1;12(4):1424-1428. eCollection 2019.
5
Hamartoma of mature cardiomyocytes in right atrium: A case report and literature review.右心房成熟心肌细胞错构瘤:一例报告及文献复习
Medicine (Baltimore). 2019 Aug;98(31):e16640. doi: 10.1097/MD.0000000000016640.