Verma Rajesh, Praharaj Heramba Narayan, Patil Tushar B, Giri Prithvi
Department of Neurology, Chhatrapati Shahuji Maharaj Medical University, Lucknow, Uttar Pradesh, India.
BMJ Case Rep. 2012 Sep 24;2012:bcr2012007094. doi: 10.1136/bcr-2012-007094.
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.
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。