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原位心脏移植术后诊断为心脏结节病,临床表现酷似致心律失常性右室心肌病。

Cardiac sarcoidosis diagnosed after orthotopic heart transplantation and clinically mimicking arrhythmogenic right ventricular cardiomyopathy.

作者信息

Makhdumi Madiha, Assar Manish D, Meyer Dan M, Roberts William C

机构信息

Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, Texas, United States.

Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, Texas, United States; Internal Medicine, Baylor University Medical Center, Dallas, Texas, United States.

出版信息

Cardiovasc Pathol. 2022 Jan-Feb;56:107390. doi: 10.1016/j.carpath.2021.107390. Epub 2021 Sep 30.

DOI:10.1016/j.carpath.2021.107390
PMID:34600147
Abstract

Described herein is a 71-year-old man who underwent orthotopic heart transplant (OHT) for chronic severe heart failure secondary to cardiac sarcoidosis (CS) devoid of non-caseating granulomas but nevertheless characteristic of CS. Clinically, his heart disease had suggested the presence of arrhythmogenic right ventricular cardiomyopathy.

摘要

本文描述了一名71岁男性,他因心脏结节病(CS)继发的慢性重度心力衰竭接受了原位心脏移植(OHT),该患者没有非干酪样肉芽肿,但仍具有CS的特征。临床上,他的心脏病提示存在致心律失常性右室心肌病。

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Cardiac sarcoidosis diagnosed after orthotopic heart transplantation and clinically mimicking arrhythmogenic right ventricular cardiomyopathy.原位心脏移植术后诊断为心脏结节病,临床表现酷似致心律失常性右室心肌病。
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引用本文的文献

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Clinical and genetic features of arrhythmogenic cardiomyopathy: diagnosis, management and the heart failure perspective.致心律失常性心肌病的临床与遗传特征:诊断、管理及心力衰竭视角
Prog Pediatr Cardiol. 2021 Dec;63. doi: 10.1016/j.ppedcard.2021.101459. Epub 2021 Nov 2.