Vrtal Jiří, Plášek Jiří, Václavík Jan, Šipula David, Dodulík Jozef
Department of Internal Medicine and Cardiology, Faculty of Medicine, University Hospital Ostrava, University of Ostrava, 17. listopadu 1790, 708 52 Ostrava, Czech Republic.
Research Center for Internal and Cardiovascular Diseases, Faculty of Medicine, University of Ostrava, 17. listopadu 1790, 708 52 Ostrava,Czech Republic.
Eur Heart J Case Rep. 2024 Dec 18;9(1):ytae673. doi: 10.1093/ehjcr/ytae673. eCollection 2025 Jan.
Charcot-Marie-Tooth is the most common inherited neuromuscular disorder. Rarely, it can be associated with heart failure and various arrhythmic disturbances. This case illustrates the challenges of making decisions to prevent sudden cardiac death in a patient with Charcot-Marie-Tooth disease.
A 69-year-old male with a history of Type 1A Charcot-Marie-Tooth disease was admitted due to repetitive runs of ventricular tachycardia. Twelve-lead electrocardiogram, echocardiography, selective coronary angiography, and cardiac magnetic resonance did not clarify the cause of the electrical storm. As conservative therapy was not successful, radiofrequency ablation was chosen to treat the electrical storm. After this procedure, implantable cardioverter defibrillator (ICD) was implanted. The follow-up revealed severe perforation by the ventricular lead. An extraction was performed with no complications and a new lead was immediately implanted. The patient remains asymptomatic. Three episodes of non-sustained ventricular tachycardia were recorded during the last follow-up.
This case illustrates the challenges of making decisions to prevent sudden cardiac death in a patient with Charcot-Marie-Tooth disease after successful ablation for electrical storm. Due to a lack of evidence, atypical origin of arrhythmia, and clinical presentation, we did not consider this as idiopathic arrhythmia and decided to implant an ICD, which was complicated by severe perforation by the lead. Specific recommendations for preventing sudden cardiac death in rare cardiac conditions, such as Charcot-Marie-Tooth disease, still need to be refined.
夏科-马里-图思病是最常见的遗传性神经肌肉疾病。它很少与心力衰竭和各种心律失常相关。本病例说明了在一名患有夏科-马里-图思病的患者中做出预防心源性猝死决策时所面临的挑战。
一名69岁男性,有1A型夏科-马里-图思病病史,因反复发作室性心动过速入院。十二导联心电图、超声心动图、选择性冠状动脉造影和心脏磁共振成像均未明确电风暴的病因。由于保守治疗未成功,选择射频消融术治疗电风暴。该手术后,植入了植入式心脏复律除颤器(ICD)。随访发现心室导线严重穿孔。进行了导线拔除,无并发症,并立即植入了新的导线。患者仍无症状。在最后一次随访期间记录到3次非持续性室性心动过速发作。
本病例说明了在成功消融电风暴后,为一名患有夏科-马里-图思病的患者做出预防心源性猝死决策时所面临的挑战。由于缺乏证据、心律失常的非典型起源和临床表现,我们未将其视为特发性心律失常,并决定植入ICD,但出现了导线严重穿孔的并发症。对于预防罕见心脏疾病(如夏科-马里-图思病)的心源性猝死的具体建议仍需完善。