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西尼罗河病毒并发纵向广泛横贯性脊髓炎和软脑膜炎:1例罕见病例报告

Concurrent Longitudinal Extensive Transverse Myelitis and Leptomeningitis in West Nile Virus: A Report of a Rare Case.

作者信息

Joseph Ivanna, Vadlamuri Diamler, Rivera Agosto Ivia E, Ghasemi Mehdi

机构信息

Department of Neurology, Lahey Hospital and Medical Center, Burlington, USA.

出版信息

Cureus. 2024 Feb 6;16(2):e53705. doi: 10.7759/cureus.53705. eCollection 2024 Feb.

Abstract

Here we report a rare case with concurrent longitudinal extensive transverse myelitis (LETM) and leptomeningitis due to West Nile virus infection. A 47-year-old man initially presented with a six-day progressive, intermittent low-grade fever, headache, diplopia, malaise, myalgia, lower back pain, and difficulty walking that developed into progressive asymmetric paralysis. Initial lab work was notable for mild lactic acidosis and hyperCKemia. Brain MRI with contrast demonstrated small foci of leptomeningeal enhancement in the cerebellum, pons, medulla, and right CN VI at the cisternal segment. MRI of the spine was remarkable for edema in the spinal cord extending from T to L with diffuse enlargement of the cord contour at T to L and subtle enhancement of nerve roots within the thecal sac and cauda equina regions. The patient responded partially to five-day intravenous immunoglobulin therapy (total dose, 2 g/kg). Electromyography four months after the onset of symptoms also showed chronic reinnervation with active denervating features in thoracolumbar myotomes. Clinically, this case highlights the ill-defined and non-specific nature of the presentation of West Nile neuroinvasive disease. It can pose a diagnostic challenge for clinicians and, if unrecognized, is associated with significant morbidity and mortality in older and compromised individuals.

摘要

在此,我们报告一例罕见病例,该病例因西尼罗河病毒感染并发纵向广泛横贯性脊髓炎(LETM)和软脑膜炎。一名47岁男性最初表现为持续6天的进行性、间歇性低热、头痛、复视、不适、肌痛、下背部疼痛以及行走困难,随后发展为进行性不对称性瘫痪。初始实验室检查显示轻度乳酸酸中毒和高肌酸激酶血症。增强脑MRI显示小脑、脑桥、延髓以及脑池段右侧第VI对脑神经有小片状软脑膜强化。脊柱MRI显示脊髓从T节段至L节段水肿,T节段至L节段脊髓轮廓弥漫性增粗,硬膜囊和马尾区域神经根有轻微强化。患者对为期5天的静脉注射免疫球蛋白治疗(总剂量2 g/kg)有部分反应。症状出现4个月后的肌电图检查也显示胸腰段肌节有慢性再支配并伴有活跃的失神经特征。临床上,该病例凸显了西尼罗河神经侵袭性疾病表现不明确和非特异性的特点。它可能给临床医生带来诊断挑战,若未被识别,在老年人和身体虚弱者中会导致显著的发病率和死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6caa/10919167/669f8ad0f199/cureus-0016-00000053705-i01.jpg

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