D. Sokolov, E. Zhelyakov, V. V. Koval’chuk, N. V. Kondratova, V. A. Snezhitskij, L. V. Kalatsei, Y. Belenkov, A. Ardashev
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引用次数: 0
摘要
遗传性运动和感觉1A型神经病(又称charcott - marie - tooth病)是一种周围神经疾病,其特征是进行性多神经病变,优先损害远端肢体肌肉。在这种病理中,对心血管系统的损害是极其罕见和异质性的。此病不包括在介入抗心律失常辅助的适应症清单中。我们无法在现有文献中找到与此病理相关的窦结功能障碍发展的临床描述。目前的临床报告提出了一个病例的检测和成功的治疗损害心血管系统表现为窦结功能障碍/病态窦综合征的变异型。采用射频导管消融、植入永久性起搏器、抗心律失常治疗以及运动感觉神经病变的药物和非药物治疗相结合的联合治疗方法,可恢复和长期维持窦性心律,并使患者的神经状态得到有益的改变。
[Clinical case of the cardiovascular system involvement in a patient with Charcot-Marie-Tooth disease].
Hereditary motor and sensory type 1A neuropathy (known as Charcot-Marie-Tooth disease) is a disease of peripheral nerves characterized by symptoms of progressive polyneuropathy with preferential damage of distal extremity muscles. Damage to the cardiovascular system is extremely rare and heterogenous in this pathology. This disease is not included in the list of indications for interventional antiarrhythmic aid. We could not find in available literature a clinical description of the development of sinus node dysfunction associated with this pathology. The present clinical report presents a case of detection and successful treatment of a damage to the cardiovascular system that manifested itself as sinus node dysfunction/sick sinus syndrome in the tachy-brady variant. A combination treatment approach using radiofrequency catheter ablation, implantation of a permanent pacemaker, and antiarrhythmic therapy associated with drug and non-drug treatment of motor sensory neuropathy resulted in recovery and long-term maintenance of sinus rhythm as well as in beneficial changes in the patient's neurological status.