Imaging Patterns of Cardiovascular Involvement in Mixed Connective Tissue Disease Evaluated by Cardiovascular Magnetic Resonance.

S. Mavrogeni, P. Sfikakis, T. Dimitroulas, L. Koutsogeorgopoulou, G. Karabela, G. Katsifis, E. Stavropoulos, E. Gialafos, G. Spiliotis, G. Kolovou, G. Kitas
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引用次数: 11

Abstract

BACKGROUND To clarify the imaging patterns of cardiovascular lesions in patients with mixed connective tissue disease (MCTD) and cardiovascular symptoms with or/ without abnormal routine non-invasive evaluation. PATIENTS-METHODS Twenty-two MCTD patients (19F/3M), aged 38±4 yrs with cardiovascular symptoms were evaluated using a 1.5 T scanner. Of them, 8/22 had systemic lupus erythematosus (SLE), 5/22 rheumatoid arthritis (RA), 5/22 scleroderma (SSc) and 4/22 myositis (MY) overlap syndromes; 10/22 patients with MCTD presented with Raynaud phenomenon (RP) and all were positive for Anti-RNP antibodies. The cardiovascular magnetic resonance study (CMR) included evaluation of function, inflammation and fibrosis. Myocardial stress perfusion-fibrosis evaluation was performed only in MCTD patients with RP. RESULTS A positive CMR study was identified in 4/8 with SLE, 1/5 with RA, 4/5 with SSc and in 1/4 with MY like MCTD. The CMR lesions were subendocardial or transmural LGE following the distribution of coronary arteries, intramyocardial LGE and diffuse subendocardial LGE in SLE-RA, MY and SSc like MCTD, respectively. Although no evidence of fibrosis was identified in patients with RP, adenosine stress myocardial perfusion revealed diffuse subendocardial perfusion defects. No correlation between disease duration and/or inflammatory indices and cardiac lesions was identified. CONCLUSION CMR can reveal myocardial lesions in MCTD patients with cardiac symptoms including myocardial infarction, inflammation, diffuse subendocardial fibrosis and diffuse perfusion defects, necessitating further cardiac investigation and/or treatment.
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心血管磁共振评价混合性结缔组织病累及心血管的成像模式。
背景:明确伴有或/不伴有异常常规无创评估的混合性结缔组织病(MCTD)合并心血管症状患者心血管病变的影像学模式。患者-方法22例MCTD患者(19F/3M),年龄38±4岁,有心血管症状,采用1.5 T扫描。其中系统性红斑狼疮(SLE)患者占8/22,类风湿关节炎(RA)患者占5/22,硬皮病(SSc)患者占5/22,肌炎(MY)患者占4/22;10/22 MCTD患者出现雷诺现象(RP),抗rnp抗体均阳性。心血管磁共振研究(CMR)包括功能、炎症和纤维化的评估。心肌应激灌注-纤维化评价仅在伴有RP的MCTD患者中进行。结果4/8的SLE、1/5的RA、4/5的SSc和1/4的MY like MCTD的CMR研究中sa阳性。CMR病变分别为冠状动脉分布的心内膜下或经壁性LGE, slel - ra、MY和SSc如MCTD的心内膜下LGE和弥漫性心内膜下LGE。虽然在RP患者中没有发现纤维化的证据,但腺苷应激心肌灌注显示弥漫性心内膜下灌注缺陷。没有发现疾病持续时间和/或炎症指数与心脏病变之间的相关性。结论cmr可显示有心肌梗死、炎症、弥漫性心内膜下纤维化、弥漫性灌注缺损等心脏症状的MCTD患者的心肌病变,提示进一步的心脏检查和/或治疗。
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