Sato Akinori, Hasegawa Yuki, Haniu Hisanori, Shiraishi Shuichi, Yagihara Nobue, Iijima Kenichi, Izumi Daisuke, Minamino Tohru
Department of Cardiovascular Biology and Medicine, Niigata University Graduate School of Medical and Dental Sciences.
Department of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences.
Int Heart J. 2019 Sep 27;60(5):1206-1210. doi: 10.1536/ihj.19-076. Epub 2019 Sep 4.
A 7-year-old female suffering from syncope attacks and deafness was genetically diagnosed with Jervell and Lange-Nielsen syndrome (JLNS). A transvenous-designed shock lead and implantable cardioverter-defibrillator (ICD) were atypically implanted subcutaneously, because the patient's body was small. Six years after implantation, we confirmed the patient's eligibility for a subcutaneous ICD (S-ICD) based on electrocardiogram screening. The implanted ICD system was replaced with a new standard S-ICD system. Implantation of the S-ICD may be considered a reliable and safe option in young patients with JLNS, even if their electrocardiograms show remarkable prolongation of the QT interval and T-wave alternans.
一名患有晕厥发作和耳聋的7岁女性经基因诊断为杰韦尔和朗格-尼尔森综合征(JLNS)。由于患者体型小,经静脉设计的除颤导线和植入式心脏复律除颤器(ICD)被非典型地皮下植入。植入后六年,我们通过心电图筛查确认患者适合皮下植入式心律转复除颤器(S-ICD)。将植入的ICD系统更换为新的标准S-ICD系统。对于患有JLNS的年轻患者,即使其心电图显示QT间期显著延长和T波交替,植入S-ICD也可能被认为是一种可靠且安全的选择。