Prolonged Limb and Respiratory Muscle Weakness Associated with Japanese Encephalitis Virus Infection: A Case Report

Sun Hong, Seoyeong Park, Yeji Lee, R. Lee, Sung Eun Hyun
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Abstract

Patients diagnosed with Japanese encephalitis (JE) may present with flaccid paralysis. JE has also been reported to be accompanied by anterior horn cell disease or motor axonal polyneuropathy. We report a case of a patient with JE with prolonged limb and respiratory muscle weakness who underwent electrodiagnostic studies, including a phrenic nerve conduction study, 10 months after the onset of paralysis. During that 10-month period, severe weakness of the upper and lower extremities showed no recovery, and the patient required long-term ventilator support through a tracheostomy. Nerve conduction studies and electromyography revealed chronic anterior horn cell disease with abundant denervation potentials involving the craniobulbar, cervical, thoracic, and lumbosacral segments. In addition to the nerves in the upper and lower extremities, the phrenic motor nerves showed abnormalities indicative of diaphragmatic weakness. Therefore, in patients with JE with chronic limb weakness and respiratory difficulty, thorough electrodiagnostic studies should be performed to diagnose the combination of anterior horn cell disease with encephalitis and to evaluate the condition’s severity and prognosis.
日本脑炎病毒感染相关肢体延长及呼吸肌无力1例报告
诊断为日本脑炎(JE)的患者可能表现为弛缓性麻痹。乙脑也有报道伴有前角细胞病或运动轴突多发性神经病。我们报告一例伴有肢体延长和呼吸肌无力的乙脑患者,他在麻痹发作10个月后接受了电诊断研究,包括膈神经传导研究。在这10个月的时间里,严重的上肢和下肢无力没有恢复,患者需要通过气管切开术长期呼吸机支持。神经传导研究和肌电图显示慢性前角细胞病具有丰富的去神经支配电位,累及颅球、颈、胸和腰骶节段。除了上肢和下肢的神经外,膈运动神经也出现异常,表明膈肌无力。因此,对于伴有慢性肢体无力和呼吸困难的乙脑患者,应进行深入的电诊断研究,以诊断前角细胞病合并脑炎,并评估病情的严重程度和预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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