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日本脑炎病毒感染后急性横贯性脊髓炎:一种常见疾病的罕见并发症。

Acute transverse myelitis following Japanese encephalitis viral infection: an uncommon complication of a common disease.

作者信息

Verma Rajesh, Praharaj Heramba Narayan, Patil Tushar B, Giri Prithvi

机构信息

Department of Neurology, Chhatrapati Shahuji Maharaj Medical University, Lucknow, Uttar Pradesh, India.

出版信息

BMJ Case Rep. 2012 Sep 24;2012:bcr2012007094. doi: 10.1136/bcr-2012-007094.

Abstract

Japanese encephalitis (JE) is an epidemic encephalitis characterised by altered sensorium, convulsions, headache, brainstem signs with pyramidal and extrapyramidal features. Immune-mediated manifestation as acute transverse myelitis (ATM) has not been previously reported in JE. We describe a 40-year-old man who presented with an acute onset quadriparesis with urinary retention, which was preceded by fever and headache 3 weeks prior. He had elevated IgM titres against JE virus in serum and cerebrospinal fluid. MRI of cervico-thoracic spine demonstrated signal intensity alterations extending from C1 to D10 spinal segments. The patient was treated with intravenous methyl prednisolone for 5 days. He regained normal power at 6 months follow-up and repeat MRI study demonstrated complete resolution of the lesion. We conclude that in a case of JE, one should be vigilant for early diagnosis of possible complication as ATM, in which an early institution of immunomodulator therapy prevents adverse consequences.

摘要

日本脑炎(JE)是一种流行性脑炎,其特征为意识改变、惊厥、头痛、伴有锥体束和锥体外系特征的脑干体征。免疫介导的表现如急性横贯性脊髓炎(ATM)此前在日本脑炎中尚未见报道。我们描述了一名40岁男性,他急性起病,出现四肢瘫并伴有尿潴留,在此之前3周有发热和头痛症状。他的血清和脑脊液中抗日本脑炎病毒的IgM滴度升高。颈胸段脊柱的MRI显示信号强度改变,范围从C1至D10脊髓节段。该患者接受了5天的静脉注射甲泼尼龙治疗。在6个月的随访中他恢复了正常肌力,重复MRI检查显示病变完全消退。我们得出结论,对于日本脑炎病例,应警惕可能并发的急性横贯性脊髓炎的早期诊断,早期应用免疫调节剂治疗可预防不良后果。

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Estimated global incidence of Japanese encephalitis: a systematic review.全球估计的日本脑炎发病率:系统评价。
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Anterior horn cells are also involved in Japanese encephalitis.前角细胞也参与日本脑炎。
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