Mohammadzadeh Ali, Houshmand Golnaz, Pouraliakbar Hamidreza, Soltani Zeinab, Salehabadi Ghazaleh, Azimi Amir, Shabanian Reza
Rajaie Cardiovascular Medical and Research Center, Iran University of medical sciences, Tehran, Iran.
Children`s Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Radiol Case Rep. 2023 Aug 10;18(10):3699-3703. doi: 10.1016/j.radcr.2023.07.062. eCollection 2023 Oct.
Immunoglobulin G4-related disease (IgG4-RD) is a chronic fibro-inflammatory disorder of obscure etiology characterized by significant infiltration of IgG4-positive plasma cells toward several organs. Coronary artery involvement is rarely seen in IgG4-RD patients; thereby, we aim to outline the noninvasive imaging findings of this rare case. Cardiac magnetic resonance (CMR) and coronary computed tomography angiography (CCTA) from a 15-year-old female diagnosed with IgG4-RD via histopathological assessment of orbital biopsy, were analyzed. CMR showed a severely reduced left ventricular ejection fraction and akinesia of the basal to mid-lateral, anterior, and septal walls. Inflammation of the basal to apical lateral wall and subendocardial infarction of the basal to apical lateral and mid inferoseptal walls were also evident. CCTA findings showed stenosis in branches of the left main artery (LM), left anterior descending artery (LAD), and right coronary artery (RCA), aortitis, and aortic wall thickening. After courses of proper treatment with prednisolone, Cellcept, and adalimumab, follow-up CMR showed significant improvement in LV systolic function and resolution of inflammation. Although IgG4-RD is an uncommon cause of coronary artery disease, it can cause lethal complications such as myocardial infarction. Hence, clinicians should be aware of cardiac complications in these patients.
免疫球蛋白G4相关性疾病(IgG4-RD)是一种病因不明的慢性纤维炎症性疾病,其特征是IgG4阳性浆细胞大量浸润多个器官。IgG4-RD患者很少出现冠状动脉受累;因此,我们旨在概述这一罕见病例的非侵入性影像学表现。对一名15岁女性进行了分析,该女性经眼眶活检组织病理学评估诊断为IgG4-RD,进行了心脏磁共振成像(CMR)和冠状动脉计算机断层扫描血管造影(CCTA)检查。CMR显示左心室射血分数严重降低,基底至中外侧、前壁和间隔壁运动减弱。基底至心尖侧壁炎症以及基底至心尖侧壁和中下部间隔壁心内膜下梗死也很明显。CCTA结果显示左主干(LM)、左前降支(LAD)和右冠状动脉(RCA)分支狭窄、主动脉炎和主动脉壁增厚。在使用泼尼松龙、骁悉和阿达木单抗进行适当治疗后,随访CMR显示左心室收缩功能显著改善,炎症消退。虽然IgG4-RD是冠状动脉疾病的罕见病因,但它可导致心肌梗死等致命并发症。因此,临床医生应意识到这些患者的心脏并发症。