Chronic Lyme neuroborreliosis

Biljana Srećković, S. Knežević, S. Đorđević
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Abstract

Introduction. Lyme neuroborreliosis is an infectious disorder of the central and/or peripheral nervous system caused by the tick stump of the genus Ixodes rici, infected with species Borrelia burgdorferi sensu lato (in Europe). The disease manifests as meningitis, encephalitis, meningoradiculitis, vasculitis, paresthesia of the facial nerve and painful radiculopathy. Case report. A 44-year-old patient reports fatigue, forgetfulness, headache, confusion, depression, drowsiness, irritability, instability, her undercooks are crushed, sheeps of a bride and does not recall being called an object. Muscular reflexes of the undergrowth are reduced. Plantar response flexion, Lazarevic sign is positive at 45 degrees from the surface. No weakness of the dorsal and plantar flexion of the fingers of the feet. Relieves sensitivity in the region of inertia nerv peroneus and tibialis. Sphincters were fine. The patient had a diagnosed Lyme disease, five months prior to the exacerbation of anxiety. Due to erythema migrans and subfebrility, diagnosis and seropositivity to Borrelia burgdorferi were established in both classes of the enzymelinked immunosorbent assay antibodies and a confirmed Western blot test. She took doxycycline 200 milligrams/day, three weeks. The analysis of cerebrospinal fluid revealed proteinhorn (0.42 g/L), normal glycorrhachia, pleocytosis, and positive intrathecal IgG antibodies. Electromyography pointed to axonal degeneration of the lower extremities. The magnetic resonance is neat. The therapy includes ceftriaxone, 2 grams/day, vitamins and analgesic therapy. Neuroborreliois was maintained by the laboratory during one-year follow-up. Mental disorders, headaches, confusion and irritability, neurological signs have significantly regressed. Conclusion. The gold standard in diagnostics of neuroborelliosis is the determination of intrathecal antibodies. For the definitive diagnosis, clinical signs of disease, pleocytosis and positive antibodies are necessary. Intrathecal antibodies remain long positive and they are not recommended for monitoring for the effects of therapy.
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慢性莱姆病
介绍。莱姆性神经疏螺旋体病是一种中枢和/或周围神经系统的传染性疾病,由感染了感氏伯氏疏螺旋体(欧洲)的里奇伊蚊属蜱残肢引起。该病表现为脑膜炎、脑炎、脑膜根炎、血管炎、面神经感觉异常和疼痛性神经根病。病例报告。一名44岁的病人报告疲劳,健忘,头痛,神志不清,抑郁,嗜睡,易怒,不稳定,她的腹部被压碎,新娘的羊群,不记得被称为物体。灌木的肌肉反射减少。足底反应屈曲,拉扎雷维奇征在离表面45度处呈阳性。没有脚背和足底屈曲的手指无力。缓解腓骨神经和胫肌惯性区的敏感性。括约肌没问题。患者在焦虑加重前5个月确诊为莱姆病。由于移行性红斑和低热,两类酶联免疫吸附试验抗体和确认的Western blot试验均确定了伯氏疏螺旋体的诊断和血清阳性。她每天服用强力霉素200毫克,持续三周。脑脊液分析显示蛋白角(0.42 g/L),糖根正常,细胞增多,鞘内IgG抗体阳性。肌电图显示下肢轴突变性。磁共振很简洁。治疗包括头孢曲松,2克/天,维生素和镇痛治疗。神经疏螺旋体在1年随访期间由实验室维持。精神障碍、头痛、神志不清、易怒、神经系统症状均明显消退。结论。神经胶质细胞病诊断的金标准是鞘内抗体的测定。对于明确的诊断,临床症状,多细胞增多症和抗体阳性是必要的。鞘内抗体长期呈阳性,不建议用于监测治疗效果。
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