心脏结节病的PET/CT评估。

IF 1.3 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Alexander Liu, Lionel T Munemo, Nuno Martins, Vasileios Kouranos, Athol U Wells, Rakesh K Sharma, Kshama Wechalekar
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引用次数: 0

摘要

18F-FDG PET结合CT是一种重要的先进成像方式,用于评估疑似或已知的心脏结节病(CS)患者。18F-FDG PET适用于有CS外征和心脏受累性筛查结果异常的患者、年龄在60岁以下出现原因不清的高级别房室传导阻滞的患者、疑似CS和特发性室性心律失常的患者进行CS检查。在已确诊的CS患者中,连续18F-FDG PET可用于评估对免疫抑制治疗的反应,以及对低级别或静止疾病患者心肌炎症再激活的长期监测。18F-FDG PET扫描前的患者准备是确保充分抑制生理性心肌18F-FDG摄取的关键,以最大限度地提高检测病理的能力。在没有活动性炎症的情况下,饮食准备不足可引起弥漫性或病灶对弥漫性18F-FDG摄取。评估静息心肌灌注非常重要,通常采用82Rb心脏PET。CS患者有几种不同的异常模式,包括心肌灌注正常,伴有局灶性或斑片状的18F-FDG摄取,提示心肌炎症但无瘢痕形成;心肌灌注缺损伴18F-FDG摄取异常提示心肌瘢痕形成伴炎症;心肌灌注缺损,无18F-FDG摄取,表明心肌瘢痕形成,无炎症。预后方面,心肌灌注缺陷和异常18F-FDG摄取已被证明是死亡或室性心律失常的独立预测因子。左、右心室的高心肌SUVmax已被证明是不良临床结果的独立预测因子。虽然对18F-FDG PET的诊断性能进行了研究,但CS的参考标准往往依赖于临床标准,在检测CS方面可能不如18F-FDG PET灵敏。因此,CS的诊断应依靠多学科团队的方法,包括超声心动图、心血管MR和18F-FDG PET等多模式高级成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of Cardiac Sarcoidosis with PET/CT.

18F-FDG PET with CT is an important advanced imaging modality used to assess patients with suspected or known cardiac sarcoidosis (CS). 18F-FDG PET is indicated for CS work-up in patients with extra-CS and abnormal screening results for cardiac involvement, patients under 60 y old presenting with unexplained high-grade atrioventricular heart block, and patients with suspected CS and idiopathic ventricular arrhythmias. In patients with established CS, serial 18F-FDG PET can be used to assess response to immunosuppressive therapy and long-term surveillance for reactivation of myocardial inflammation in patients with low-grade or quiescent disease. Patient preparation before 18F-FDG PET scanning is key in ensuring adequate suppression of physiologic myocardial 18F-FDG uptake, to maximize the power of the test to detect pathology. Inadequate dietary preparation can cause diffuse or focal-on-diffuse 18F-FDG uptake in the absence of active inflammation. It is important to assess resting myocardial perfusion, typically with 82Rb cardiac PET. Several different patterns of abnormalities have been reported in patients with CS, including normal myocardial perfusion with focal or patchy 18F-FDG uptake suggesting myocardial inflammation without scarring; the presence of a myocardial perfusion defect with abnormal 18F-FDG uptake suggesting myocardial scarring with inflammation; and the presence of a myocardial perfusion defect without 18F-FDG uptake indicating myocardial scarring without inflammation. Prognostically, the presence of myocardial perfusion defects and abnormal 18F-FDG uptake has been shown to be an independent predictor of death or ventricular arrythmias. A high myocardial SUVmax in the left and right ventricles has been shown to be an independent predictor of adverse clinical outcomes. Although the diagnostic performance of 18F-FDG PET has been studied, the reference standard for CS tended to rely on clinical criteria, which may be less sensitive than 18F-FDG PET at detecting CS. Therefore, the diagnosis of CS should rely on a multidisciplinary team approach involving multimodality advanced imaging, including echocardiography, cardiovascular MR, and 18F-FDG PET.

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来源期刊
Journal of nuclear medicine technology
Journal of nuclear medicine technology RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
CiteScore
1.90
自引率
15.40%
发文量
57
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