Lim Kyunghee, Park Jong Sung, Yoon Byeol-A, Han Song-Hee
Department of Cardiology, Dong-A University Hospital, 32 Daesingongwon-ro, Seo-gu, Busan 49202, Korea.
Department of Neurology, Dong-A University Hospital, 32 Daesingongwon-ro, Seo-gu, Busan 49202, Korea.
Eur Heart J Case Rep. 2021 Jun 16;5(6):ytab075. doi: 10.1093/ehjcr/ytab075. eCollection 2021 Jun.
Necrotizing autoimmune myopathy is a rare subtype of idiopathic inflammatory myopathy; however, it can be associated with fatal cardiac manifestations.
A 58-year-old female patient was referred for congestive heart failure with dysrhythmia. Electrocardiograms showed ventricular arrhythmias of various QRS complex morphologies and coupling intervals with beat-to-beat differences. Despite optimal medical therapy for heart failure, the patient was admitted for the progression of dyspnoea and generalized motor weakness. The burden of non-sustained ventricular tachycardia gradually increased, and ventricular fibrillation eventually occurred. In view of a differential diagnosis of an inflammatory myocardial diseases such as sarcoidosis, a cardiac biopsy was performed. However, pathologic examinations revealed only necrotic muscle fibres without granuloma. Further examinations revealed proximal dominant motor weakness, an elevated serum creatinine-phosphokinase level, myogenic potentials on needle electromyography, and biceps muscle biopsy findings that were compatible with necrotizing autoimmune myopathy. High-dose steroid therapy improved the patient's motor weakness, including her respiratory impairment, and successfully suppressed ventricular arrhythmias.
This case suggests that intensive immunosuppressive therapy with high-dose steroid could be useful in the necrotizing autoimmune myopathy manifested as congestive heart failure and life-threatening ventricular arrhythmias.
坏死性自身免疫性肌病是特发性炎性肌病的一种罕见亚型;然而,它可伴有致命的心脏表现。
一名58岁女性患者因充血性心力衰竭伴心律失常前来就诊。心电图显示室性心律失常,QRS波群形态各异,联律间期逐搏不同。尽管对心力衰竭进行了最佳药物治疗,但患者仍因呼吸困难进展和全身肌无力入院。非持续性室性心动过速的负担逐渐增加,最终发生心室颤动。鉴于需鉴别诊断结节病等炎性心肌疾病,遂进行了心脏活检。然而,病理检查仅发现坏死的肌纤维,无肉芽肿。进一步检查发现近端为主的肌无力、血清肌酸磷酸激酶水平升高、针极肌电图显示肌源性电位,以及肱二头肌活检结果与坏死性自身免疫性肌病相符。大剂量类固醇治疗改善了患者的肌无力,包括呼吸功能障碍,并成功抑制了室性心律失常。
该病例表明,大剂量类固醇强化免疫抑制治疗对表现为充血性心力衰竭和危及生命的室性心律失常的坏死性自身免疫性肌病可能有效。