Management Of Neuroretinitis In A Case of Lyme Disease

S. Nainiwal, S. Kumari, Balbir Singh, R. Yadav
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Abstract

Neuroretinitis in Lyme disease is a rare entity, which is caused by Borrelia burgdorferi. Diagnosis of the disease is based on clinical history, symptoms and serological testing. Here, we present a case of a young 12 year old female suffering from unilateral neuroretinitis associated with Lyme disease characterized by sudden loss of vision, optic disc swelling and macular star. After the diagnosis, the patient received medical therapy and improved well. Early diagnosis and appropriate management of this disease may improve vision with a good outcome. relative afferent pupillary defect in the left eye. Colour vision was defective in the left eye. Extraocular motility and confrontational visual fields were full in both eyes but on Humphry field analyzer, there was centroceacal scotoma noted in the left eye. Intraocular pressure was 12.2mmHg in both eyes. Slit lamp examination of both eyes was unremarkable with no evidence of anterior chamber and anterior vitreous cells. Fundus examination revealed optic disc oedema with hard exudates arranged in a macular star pattern in the left eye (Figure-1a). Fluorescein angiography confirmed our diagnosis of neuroretinitis (Figure-1b). Routine blood investigations were within normal limits but serological testing showed positive IgM antibodies for Borrelia, suggestive of Lyme disease. After diagnosis of the case as neuroretinitis due to Lyme disease, the patient received intravenous infusion of methylprednisolone750mg in 150ml GDW in 45minutes for three consecutive days with intravenous ceftriaxone 500mg QID daily for 21 days. After pulse therapy of methylprednisolone for 3 days, the patient was switched on oral prednisolone with a dose of 20mg once a day with capsule omeprazole 10mg empty Abstract stomach for another 2 weeks. After 3 days of pulse therapy, the patient’s vision improved to the level of 6/6 in the right eye and 6/12 in the left eye, and at 1 month follow up, the patient’s vision was 6/6 in both eyes. After one month post treatment, there was marked decrease in disc oedema noted clinically and angiographically (Figure-2a & 2b). Repeat serological test after one month treatment showed low titer of IgG antibodies and absence of IgM antibodies for Borrelia.
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莱姆病1例神经视网膜炎的治疗
莱姆病中的神经视网膜炎是一种罕见的疾病,由伯氏疏螺旋体引起。该病的诊断基于临床病史、症状和血清学检测。在此,我们报告一位年轻的12岁女性患有单侧神经视网膜炎并伴有莱姆病,其特征是突然丧失视力,视盘肿胀和黄斑星。确诊后,患者接受药物治疗,病情好转良好。这种疾病的早期诊断和适当的治疗可以改善视力并获得良好的结果。左眼瞳孔相对传入缺损。左眼色觉有缺陷。双眼眼外运动和对视视野均满,但汉弗莱视野分析仪显示左眼中心凹陷。双眼眼压为12.2mmHg。双眼裂隙灯检查未见明显前房及前玻璃体细胞。眼底检查显示左眼视盘水肿伴硬渗出物呈黄斑星形排列(图1a)。荧光素血管造影证实了我们对神经视网膜炎的诊断(图1b)。常规血液检查在正常范围内,但血清学检测显示伯氏疏螺旋体IgM抗体阳性,提示莱姆病。患者诊断为莱姆病所致神经视网膜炎后,给予甲泼尼龙750mg 150ml GDW, 45min静脉滴注,连续3天,头孢曲松500mg QID,每日静脉滴注,连续21天。甲强的松龙脉冲治疗3天后,改为口服强的松龙,剂量20mg,每日1次,并联合奥美拉唑胶囊10mg空抽胃,再治疗2周。脉冲治疗3天后,患者右眼视力改善至6/6,左眼视力改善至6/12,随访1个月时,患者双眼视力为6/6。治疗一个月后,临床和血管造影显示椎间盘水肿明显减少(图2a和2b)。治疗1个月后复查血清学检查,结果显示IgG抗体滴度低,无博氏疏螺旋体IgM抗体。
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