Ali Muhammad Sajawal, Mba Benjamin I, Husain Aliya Noor, Ciftci Farah Diba
Department of Medicine, John H Stroger, Jr, Hospital of Cook County, Chicago, Illinois, USA.
Department of Pathology, University of Chicago, Chicago, USA.
BMJ Case Rep. 2016 Mar 23;2016:bcr2015213759. doi: 10.1136/bcr-2015-213759.
A 40-year-old man with a history of orbital myositis (OM) presented to the emergency department with ventricular tachycardia requiring electrical cardioversion. Postcardioversion ECG showed right bundle branch block, while an echocardiogram revealed an ejection fraction of 20% and a dilated right ventricle. Cardiac MRI produced suboptimal images because the patient was having frequent arrhythmias. The rest of the work up, including coronary angiography, was unremarkable. Given the dilated right ventricle, we suspected arrhythmogenic right ventricular cardiomyopathy and discharged the patient with an implantable cardioverter-defibrillator. 1 week later, he was readmitted with cardiogenic shock; endomyocardial biopsy revealed giant cell myocarditis (GCM). To the best of our knowledge, this is the seventh case report of GCM described in a patient with OM. We recommend that clinicians maintain a high degree of suspicion for GCM in patients with OM presenting with cardiac problems.
一名有眼眶肌炎(OM)病史的40岁男性因室性心动过速需进行电复律而就诊于急诊科。复律后的心电图显示右束支传导阻滞,而超声心动图显示射血分数为20%且右心室扩张。心脏磁共振成像(MRI)因患者频繁出现心律失常而未能获得理想图像。包括冠状动脉造影在内的其余检查均无异常。鉴于右心室扩张,我们怀疑是致心律失常性右心室心肌病,并让患者带着植入式心律转复除颤器出院。1周后,他因心源性休克再次入院;心内膜心肌活检显示为巨细胞性心肌炎(GCM)。据我们所知,这是第七例关于OM患者中出现GCM的病例报告。我们建议临床医生对于有心脏问题的OM患者要高度怀疑GCM。