Narayanan Santhosh, Thulaseedharan N K, Subramaniam Gomathy, Panarkandy Geetha, Shameer V K, Narayanan Arathi
Department of General Medicine.
Department of Radiodiagnosis, Government Medical College, Kozhikode, Kerala, India.
Int J Gen Med. 2017 Apr 12;10:125-129. doi: 10.2147/IJGM.S129829. eCollection 2017.
Japanese encephalitis (JE) is an infectious encephalitis prevalent in Asia. It usually presents with fever, headache, convulsions and extrapyramidal symptoms. Limbic system involvement and hypothermia though common in autoimmune encephalitis have never been reported in JE. We report a case of an 18-year-old girl with no previous comorbidities who presented to us with a history of fever and headache for 1 week duration. She developed bilateral lateral rectus palsy and asymmetric flaccid weakness of all four limbs, after 2 days of admission, which was followed by altered sensorium and intermittent hypothermia. Neuroimaging revealed longitudinal myelitis extending from pons till the L1 level along with bilateral thalamic hemorrhage in brain. Cerebrospinal fluid (CSF) was positive for IgM antibody to JE virus. She was treated with supportive measures, but she developed intractable hypothermia and seizures and succumbed to illness after 2 weeks of admission.
日本脑炎(JE)是一种在亚洲流行的传染性脑炎。它通常表现为发热、头痛、惊厥和锥体外系症状。边缘系统受累和体温过低在自身免疫性脑炎中虽常见,但在日本脑炎中从未有过报道。我们报告一例18岁女孩,既往无合并症,因发热、头痛1周前来就诊。入院2天后,她出现双侧外直肌麻痹和四肢不对称弛缓性无力,随后出现意识改变和间歇性体温过低。神经影像学检查显示,脑桥至L1水平的纵向脊髓炎以及双侧丘脑出血。脑脊液(CSF)中日本脑炎病毒IgM抗体呈阳性。她接受了支持性治疗,但出现了顽固性体温过低和惊厥,入院2周后死亡。