[Imaging diagnostics of cardiac sarcoidosis].

IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Herz Pub Date : 2023-10-01 Epub Date: 2023-09-08 DOI:10.1007/s00059-023-05208-z
Ron Blankstein, Stephan Achenbach
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Abstract

Cardiac involvement is clinically apparent in approximately 5% of all patients with systemic sarcoidosis, whereas evidence of cardiac involvement by imaging studies can be found in approximately 20% of cases. Occasionally, isolated cardiac sarcoidosis is encountered and is the only sign of the disease. The most frequent cardiac manifestations of the multifocal granulomatous inflammation include atrioventricular (AV) blocks and other conduction disorders, ventricular arrhythmias, sudden cardiac death and left and right ventricular wall disorders. Accordingly, symptoms that should raise suspicion include palpitations, lightheadedness and syncope. The diagnostic approach to cardiac sarcoidosis is not straightforward. Typical echocardiographic findings include regional thinning and contraction abnormalities particularly in basal, septal and lateral locations. Infrequently, myocardial hypertrophy may be present; however, the sensitivity of echocardiography is low and cardiac sarcoidosis can be present even when an echocardiogram is unrevealing. Cardiac magnetic resonance imaging (MRI) frequently shows late gadolinium enhancement (LGE) in a multifocal pattern often involving the basal septum and lateral walls. The sensitivity and specificity of MRI for detecting cardiac sarcoidosis are high. Fluorodeoxyglucose positron emission tomography (FDG-PET) plays an important role in the diagnostic algorithm due to its ability to visualize focal inflammatory activity both in the myocardium and in extracardiac locations. This may help target the optimal location for biopsy in order to obtain histologic proof of sarcoidosis and can also be used to follow the response to anti-inflammatory treatment. Notably, the sensitivity of endomyocardial biopsy is poor due to the patchy nature of myocardial involvement. In clinical practice, either histologic evidence of noncaseating granulomas from the myocardium or evidence from extracardiac tissue in combination with typical cardiac imaging findings are required to establish the diagnosis.

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[心脏结节病的影像学诊断]。
大约5%的系统性结节病患者的心脏受累在临床上是明显的,而通过影像学研究可以在大约20%的病例中发现心脏受累的证据。偶尔会遇到孤立的心脏结节病,这是该疾病的唯一迹象。多灶性肉芽肿性炎症最常见的心脏表现包括房室传导阻滞和其他传导障碍、室性心律失常、心源性猝死以及左右心室壁疾病。因此,应该引起怀疑的症状包括心悸、头晕和晕厥。心脏结节病的诊断方法并不简单。典型的超声心动图检查结果包括局部变薄和收缩异常,尤其是基底部、间隔部和外侧部。心肌肥大可能是罕见的;然而,超声心动图的敏感性很低,即使在超声心动图未显示的情况下,也可能出现心脏结节病。心脏磁共振成像(MRI)经常显示晚期钆增强(LGE)的多灶性模式,通常涉及基底隔膜和侧壁。MRI检测心脏结节病的敏感性和特异性较高。氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)由于能够显示心肌和心外部位的局灶性炎症活动,在诊断算法中发挥着重要作用。这可能有助于确定活检的最佳位置,以获得结节病的组织学证据,也可用于跟踪抗炎治疗的反应。值得注意的是,由于心肌受累的斑块性质,心肌内活检的敏感性较差。在临床实践中,需要心肌非无菌肉芽肿的组织学证据或心外组织的证据与典型的心脏成像结果相结合来确定诊断。
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来源期刊
Herz
Herz 医学-心血管系统
CiteScore
3.00
自引率
5.90%
发文量
61
审稿时长
4-8 weeks
期刊介绍: Herz is the high-level journal for further education for all physicians interested in cardiology. The individual issues of the journal each deal with specific topics and comprise review articles in English and German written by competent and esteemed authors. They provide up-to-date and comprehensive information concerning the speciality dealt with in the issue. Due to the fact that all relevant aspects of the pertinent topic of an issue are considered, an overview of the current status and progress in cardiology is presented. Reviews and original articles round off the spectrum of information provided.
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