Zhao Jingmin, Gao Yu, Jin Zhengxian, Huang Yujing, Lee Kwee-Yum, Shen Guangxun
Department of Neurology, China-Japan Union Hospital of Jilin University Changchun, Jilin, China.
Department of Orthopaedic Surgery and Musculoskeletal Medicine, University of Otago Dunedin, New Zealand.
Am J Transl Res. 2024 Feb 15;16(2):539-543. doi: 10.62347/GFEO1891. eCollection 2024.
Tachycardia-bradycardia syndrome (TBS) is a variant of sick sinus syndrome (SSS) characterized by alternating tachycardia and bradycardia. A few cases of SSS secondary to structural lesions in the medulla have been reported, but there has never been a reported case of the rare sign akin to TBS following acute non-medullary brainstem infarction. Furthermore, new-onset cardiac arrhythmias in stroke often presented in one continuous pattern - either as bradycardia or tachycardia, but instances of an alternating fashion have been rarely reported. We present the case of a 46-year-old female who developed severe dizziness with vomiting, diplopia, and slurred speech, which gradually worsened to quadriplegia, severe hypophonia, and dysphagia. Brain magnetic resonance imaging (MRI) demonstrated acute midbrain and pontine infarction. Except for neurological symptoms, the patient experienced unexpected TBS with the symptoms of excessive sweating, palpitations, and irritability without any other predisposing factors. The frequency of the episodes gradually declined until it spontaneously disappeared the 5 day after admission. Given the unpredictable nature of the tachycardia and bradycardia, it was challenging to manage the arrythmias with medications. A pacemaker was recommended, but financial reasons led the patient to reject this option. Two weeks after antithrombotic therapy and rehabilitation, she was discharged with residual symptoms of diplopia, moderate dysarthria, mild quadriplegia, and no cardiac symptoms. Our case highlighted the occurrence of TBS as a new-onset arrhythmia that can manifest during the acute phase of non-medullary brainstem infarcts. Further research into brainstem lesions contributing to TBS is warranted us to elucidate the underlying mechanisms.
心动过速-心动过缓综合征(TBS)是病态窦房结综合征(SSS)的一种变体,其特征为心动过速和心动过缓交替出现。有少数关于继发于延髓结构病变的SSS病例报道,但从未有过急性非延髓性脑干梗死之后出现类似TBS这种罕见体征的病例报道。此外,中风后新发的心律失常通常呈现一种持续的模式——要么是心动过缓,要么是心动过速,但交替出现的情况鲜有报道。我们报告一例46岁女性病例,该患者出现严重头晕伴呕吐、复视和言语含糊,病情逐渐加重至四肢瘫痪、严重声音低微和吞咽困难。脑部磁共振成像(MRI)显示急性中脑和脑桥梗死。除神经系统症状外,患者在没有任何其他诱发因素的情况下意外出现了伴有多汗、心悸和易怒症状的TBS。发作频率逐渐下降,直至入院后第5天自行消失。鉴于心动过速和心动过缓的不可预测性,用药物治疗心律失常具有挑战性。建议安装起搏器,但因经济原因患者拒绝了这一选择。抗血栓治疗和康复两周后,她出院时仍有复视、中度构音障碍、轻度四肢瘫痪等残留症状,且无心脏症状。我们的病例突出了TBS作为一种可在非延髓性脑干梗死急性期出现的新发心律失常。有必要对导致TBS的脑干病变进行进一步研究,以阐明其潜在机制。