Rasmussen Torsten Bloch, Dalager Soren, Andersen Niels Holmark, Hansen Troels Krarup, Nielsen-Kudsk Jens Erik
Aarhus University Hospital, Dept. of Cardiology B, Brendstrupgaardsvej 100, Aarhus, DK-8200 N, Denmark.
BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.09.2008.0997. Epub 2009 Apr 28.
A case of circulatory collapse due to severe heart failure is reported in a 52-year old male with autoimmune disorders in the form of type-1 diabetes, Graves' disease and total alopecia.Upon admission, the patient had severe heart failure with a cardiac index of 0.9 l/min/m(2), a mixed venous saturation of 29% and left ventricular ejection fraction of 5%. The condition was refractory to treatment with inotropic agents and required mechanical cardiopulmonary support. Endomyocardial biopsies revealed extensive giant cell myocarditis (GCM). Immunosuppressant treatment did not alter the condition and urgent orthotopic heart transplantation was performed.Histopathological examination of the explanted heart confirmed the diagnosis and showed widespread vascular deposition of complement C4d suggesting a pathogenic role for the innate immune system in GCM.At 1-year follow-up the patient was in New York Heart Association (NYHA) class I, had episodes of sustained ventricular tachycardia but showed no evidence of GCM recurrence in endomyocardial biopsies.
报道了一例52岁男性因严重心力衰竭导致循环衰竭的病例,该患者患有自身免疫性疾病,表现为1型糖尿病、格雷夫斯病和全秃。入院时,患者患有严重心力衰竭,心脏指数为0.9升/分钟/平方米,混合静脉血氧饱和度为29%,左心室射血分数为5%。该病情对强心剂治疗无效,需要机械心肺支持。心内膜活检显示广泛的巨细胞性心肌炎(GCM)。免疫抑制治疗未能改变病情,遂紧急进行原位心脏移植。移植心脏的组织病理学检查证实了诊断,并显示补体C4d广泛沉积于血管,提示先天性免疫系统在GCM中起致病作用。在1年随访时,患者纽约心脏协会(NYHA)心功能分级为I级,有持续性室性心动过速发作,但心内膜活检未显示GCM复发迹象。