Matturri L, Valente M G, Arrigoni G, Ghidoni P, Bauer E, Rossi L
Istituto di Anatomia Patologica, Università degli Studi di Milano.
Minerva Cardioangiol. 1992 Jun;40(6):239-43.
The Authors report a case of Takayasu disease in a woman who died at the age of forty-six, in whom the histological examination of the cardio-vascular system revealed giant cells granulomatous arteritis localized in the aortic arch and collateral arteries; endocarditis and granulomatous coronaritis. The bases of arrhythmogenic alterations, in this study, take into account the thrombosis of the conduction system arteriolar vessels and the phlogosis extending to the cardiac plexus.
作者报告了一例46岁女性患高安氏病的病例，该患者心血管系统的组织学检查显示，巨细胞性肉芽肿性动脉炎局限于主动脉弓和侧支动脉；心内膜炎和肉芽肿性冠状动脉炎。在本研究中，致心律失常改变的基础考虑了传导系统小动脉血管的血栓形成以及蔓延至心脏神经丛的炎症。
