Bilateral facial nerve palsy in the course of neuroborreliosis in children-dynamics, laboratory tests and treatment.

J Młodzikowska-Albrecht, M Zarowski, B Steinborn, A Winczewska-Wiktor, B Gurda, J Wigowska-Sowińska
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Abstract

Purpose: Presentation of four patients with bilateral peripheral facial nerve palsy as a clinical manifestation of neuroborreliosis in children--diagnostic, treatment and prognosis.

Material and methods: In 2002-2004 in The Chair and Department of Developmental Neurology, 24 children from the Wielkopolska region were admitted with diagnosis of borreliosis. Among all the children with borreliosis, confirmed by serologic examination, 4 (16.7%) demonstrated bilateral peripheral facial palsy (PFP). We investigated the presence of IgM class and IgG class specific antibodies in the sera and cerebrospinal fluid (CSF) of 4 patients with bilateral PFP. (Detected by immunoenzymatic methods--ELISA.)

Results: Before the occurrence of PFP all the children manifested unspecified systemic symptoms such as headaches, muscle and articulation pains, weakness and in two cases a mood depression. At first all patients demonstrated elevated IgM antibodies and proper levels of IgG antibodies. Control tests administered within 2-14 months later reduction of antibodies was indicated. Two patients demonstrated significant pleocytosis in CSF test, (without the meningeal symptoms). All children were treated with physiotherapeutic procedures and were administered antibiotic intravenously.

Conclusions: PFP is one of the most frequent neurological symptoms of borreliosis in children. In case of acute PFP and especially the bilateral form of PFP, neuroborreliosis is the most probable diagnosis. All children reported PFP at one side first and after several weeks the paresis of the facial nerve on the opposite side usually appeared. The clinical state of children started to improve after the introduction of physiotherapy and this process usually lasted several months.

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小儿神经疏螺旋体病过程中双侧面神经麻痹的动态、实验室检查和治疗。
目的:介绍4例以小儿神经疏螺旋体病为临床表现的双侧周围面神经麻痹的诊断、治疗及预后。材料和方法:2002-2004年,在主席和发育神经内科,24名来自大波兰地区的儿童被诊断为螺旋体病。在所有经血清学检查证实的螺旋体病患儿中,4例(16.7%)表现为双侧周围性面瘫(PFP)。我们检测了4例双侧PFP患者血清和脑脊液中IgM类和IgG类特异性抗体的存在。(免疫酶法——ELISA检测)结果:在PFP发生前,所有患儿均表现出未明确的全身性症状,如头痛、肌肉和关节痛、虚弱,其中2例出现情绪抑郁。首先,所有患者均表现出IgM抗体升高和适当水平的IgG抗体。在2-14个月内进行的对照试验表明抗体减少。2例患者脑脊液检查显示明显的细胞增多(无脑膜症状)。所有患儿均接受物理治疗并静脉注射抗生素。结论:PFP是小儿疏螺旋体病最常见的神经系统症状之一。对于急性PFP,特别是双侧PFP,最可能的诊断是神经螺旋体病。所有患儿首先报告一侧面神经麻痹,数周后通常出现对侧面神经麻痹。引入物理治疗后患儿的临床状态开始改善,这一过程通常持续数月。
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