Department of Internal Medicine III, Friedrich Schiller University Jena, Erlanger Allee 101, 07747 Jena, Germany.
Rheumatol Int. 2013 Jan;33(1):29-35. doi: 10.1007/s00296-011-2310-3. Epub 2012 Jan 3.
This report describes the potential of cardiac magnetic resonance imaging (cMRI) based on myocardial first-pass perfusion imaging in the visualization of cardiac manifestations in autoimmune vasculitis, which in the heart are typically localized at the level of small subendocardial vessels. Two patients with primary or secondary autoimmune vasculitis were investigated in this study. Myocardial first-pass perfusion imaging was performed using an ECG-gated T1-weighted MRI sequence after the injection of intravenous bolus of gadolinium chelate. In both cases, the cMRI showed findings of subendocardial first-pass perfusion deficit (FPPD), a phenomenon so far described as microvascular obstruction (MVO) only in patients with acute cardiac infarction due to thromboembolic obstruction of small myocardial vessels. The two patients showed local subendocardial and myocardial hypoenhancement (characterized by a darker appearance than normal myocardial tissue), which is the typical morphological stigma of FPPD initially after injection of contrast media. The perfusion deficit, although morphologically very similar to the well-known phenomenon of MVO in acute cardiac infarction, was conceivably caused by different vasculitis-specific mechanisms such as occlusion of the microvasculature with erythrocytes, neutrophils and cellular debris. This study indicates that FPPD is useful for the non-invasive assessment of the microvasculature in patients with acute cardiac involvement in primary and secondary vasculitis.
本报告描述了基于心肌首过灌注成像的心脏磁共振成像(cMRI)在自身免疫性血管炎心脏表现可视化中的潜力,在心脏中,这些表现通常定位于小的心内膜下血管水平。本研究调查了两名原发性或继发性自身免疫性血管炎患者。在注射静脉团注钆螯合物后,使用 ECG 门控 T1 加权 MRI 序列进行心肌首过灌注成像。在这两种情况下,cMRI 均显示出心内膜下首过灌注缺陷(FPPD)的发现,这一现象迄今为止仅在因小心肌血管血栓栓塞阻塞而发生急性心肌梗死的患者中被描述为微血管阻塞(MVO)。两名患者表现为局部心内膜下和心肌低增强(表现为比正常心肌组织颜色更暗),这是注射造影剂后最初 FPPD 的典型形态学特征。尽管这种灌注缺陷在形态上与急性心肌梗死中众所周知的 MVO 现象非常相似,但它可能是由不同的血管炎特异性机制引起的,如红细胞、中性粒细胞和细胞碎片阻塞微血管。这项研究表明,FPPD 可用于评估原发性和继发性血管炎中急性心脏受累患者的微血管。