Uchida Tetsuro, Hamasaki Azumi, Kuroda Yoshinori, Sadahiro Mitsuaki, Tamazawa Nobuyuki, Ohe Rintaro, Yamakawa Mitsunori
Second Department of Surgery, Faculty of Medicine, Yamagata University, Yamagata, Yamagata, Japan.
Department of Pathological Diagnosis, Faculty of Medicine, Yamagata University, Yamagata, Yamagata, Japan.
Ann Thorac Cardiovasc Surg. 2018 Aug 20;24(4):208-210. doi: 10.5761/atcs.cr.17-00111. Epub 2017 Dec 27.
Immunoglobulin G subclass 4-related disease (IgG4-RD) is a recently recognized systemic inflammatory disease characterized by an elevated serum IgG4 level and an IgG4-positive lymphocyte infiltrate mainly in exocrine tissues. Previous reports documented IgG4-RD in several cardiovascular disorders. We present a case of type A aortic dissection associated with IgG4-RD. A 52-year-old man diagnosed with a type A aortic dissection was referred for surgical treatment. He underwent emergency hemiarch reconstruction with a prosthetic graft. His postoperative recovery was uncomplicated. Histopathologic examination of his aortic tissue showed marked adventitial thickening with fibrosis and an IgG4-positive plasma cell infiltrate. He was diagnosed with type A aortic dissection incidentally complicated by IgG4-RD. The relationship between IgG4-RD and the pathogenesis of aortic dissection remains unknown and requires further investigation.
免疫球蛋白G4相关疾病(IgG4-RD)是一种最近才被认识的系统性炎症性疾病,其特征是血清IgG4水平升高以及主要在外分泌组织中的IgG4阳性淋巴细胞浸润。先前的报告记录了几种心血管疾病中的IgG4-RD。我们报告一例与IgG4-RD相关的A型主动脉夹层病例。一名被诊断为A型主动脉夹层的52岁男性被转诊接受手术治疗。他接受了人工血管紧急半弓重建术。术后恢复顺利。对其主动脉组织的组织病理学检查显示,外膜明显增厚伴纤维化以及IgG4阳性浆细胞浸润。他被诊断为A型主动脉夹层并偶然合并IgG4-RD。IgG4-RD与主动脉夹层发病机制之间的关系尚不清楚,需要进一步研究。