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以心肌缺血为表现的IgG4相关性疾病:病例回顾

Myocardial ischemia as presenting manifestation of IgG4-related disease: a case-based review.

作者信息

Delgado-García Guillermo, Sánchez-Salazar Sergio, Rendón-Ramírez Erick, Castro-Medina Mario, Sáenz-Ibarra Bárbara, Barboza-Quintana Álvaro, Loredo-Alanis María Azalea, Hernández-Barajas David, Galarza-Delgado Dionicio

机构信息

Department of Internal Medicine, University Hospital, Autonomous University of Nuevo León, Madero y Gonzalitos s/n, Col. Mitras Centro, C.P., 64460, Monterrey, México.

Division of Pulmonology and Intensive Care Unit, University Hospital, Autonomous University of Nuevo León, Monterrey, México.

出版信息

Clin Rheumatol. 2016 Nov;35(11):2857-2864. doi: 10.1007/s10067-016-3292-z. Epub 2016 May 4.

Abstract

Coronary involvement in IgG4-related disease (IgG4-RD) has been scarcely reported, and myocardial ischemia as its presenting feature is even rarer. Here, we describe an additional case with novel and relevant observations. The patient was a previously healthy, middle-aged woman who presented to the clinic with new-onset typical angina. One tumefactive lesion encasing the left anterior descending artery was found during her workup. The most common underlying malignancies with secondary cardiac involvement were rationally ruled out. Symptoms persisted despite medical treatment, and she was therefore referred to surgery. Tumor excision was successfully performed, and she received coronary bypass grafting. IgG4-related coronary arteritis with pseudotumor formation was subsequently diagnosed following the comprehensive diagnostic criteria. This condition was clinically classified as active and circulating plasmablasts were found to be increased (5480/mL), even when these were determined 38 days after surgery. A PET/CT revealed an additional hypermetabolic lymph node. She was therefore treated with rituximab as induction therapy (two 1000 mg doses, administered 15 days apart). Three months later, her disease remained clinically inactive. Circulating plasmablasts were repeated and these had dropped to 0/mL. We thereafter review the current and pertinent literature on the topic, emphasizing the previous cases with similar presenting features (n = 7). We lastly suggest that IgG4-RD should be part of the differential diagnosis of any patient with tumefactive lesions surrounding the coronary arteries, since it can initially presented as sudden cardiac death.

摘要

IgG4相关疾病(IgG4-RD)累及冠状动脉的报道极为罕见,以心肌缺血为首发表现的情况更是罕见。在此,我们描述另外一例具有新的相关观察结果的病例。该患者是一名此前健康的中年女性,因新发典型心绞痛就诊于诊所。在检查过程中发现一个包绕左前降支动脉的肿块性病变。合理排除了最常见的伴有继发性心脏受累的潜在恶性肿瘤。尽管进行了药物治疗,症状仍持续存在,因此她被转诊接受手术。成功进行了肿瘤切除,并接受了冠状动脉搭桥术。随后根据综合诊断标准诊断为IgG4相关性冠状动脉炎伴假瘤形成。这种情况临床分类为活动期,即使在术后38天测定时,发现循环浆母细胞增多(5480/mL)。PET/CT显示还有一个代谢增高的淋巴结。因此,她接受了利妥昔单抗诱导治疗(两次1000mg剂量,间隔15天给药)。三个月后,她的病情临床处于非活动期。再次检测循环浆母细胞,其已降至0/mL。我们随后回顾了关于该主题的当前及相关文献,重点介绍了具有类似表现特征的既往病例(n = 7)。我们最后建议,IgG4-RD应作为任何有冠状动脉周围肿块性病变患者鉴别诊断的一部分,因为它最初可能表现为心源性猝死。

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