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由日本脑炎病毒引起的脊髓灰质炎样疾病。

Poliomyelitis-like illness due to Japanese encephalitis virus.

作者信息

Solomon T, Kneen R, Dung N M, Khanh V C, Thuy T T, Ha D Q, Day N P, Nisalak A, Vaughn D W, White N J

机构信息

Wellcome Trust Clinical Research Unit, Cho Quan Hospital, Ho Chi Minh City, Vietnam.

出版信息

Lancet. 1998 Apr 11;351(9109):1094-7. doi: 10.1016/S0140-6736(97)07509-0.

DOI:10.1016/S0140-6736(97)07509-0
PMID:9660579
Abstract

BACKGROUND

Acute flaccid paralysis remains common among Vietnamese children despite a pronounced fall in the incidence of poliomyelitis.

METHODS

During 1995, all 22 children presenting with acute flaccid paralysis to a referral centre in Ho Chi Minh City, Vietnam, had virological cultures and antibody measurements done on serum, cerebrospinal fluid, and faeces. A year later the children were reassessed and electrophysiological studies were done.

FINDINGS

Wild poliovirus type 1 was isolated from the faeces of only one patient, and non-polio enteroviruses from three patients. 12 (55%) of the 22 children with acute flaccid paralysis had evidence of acute Japanese encephalitis virus (JEV) infection, compared with only one (1%) of 88 age-matched hospital controls (children with diphtheria; p<0.0001). Compared with JEV-negative patients, weakness in JEV-infected children was more rapid in onset, tended to be asymmetrical, but was less likely to involve the arms. All 12 children with JEV infection were febrile at the onset of weakness, seven had acute retention of urine, and ten had CSF pleiocytosis. Seven of eight JEV-negative patients met the case-definition of Guillain-Barré syndrome, compared with only one of 12 JEV-positive children. At follow-up, patients with JEV infection had greater disability and were more likely to have muscle wasting than were JEV-negative children. Nerve conduction and electromyographic studies indicated damage to the anterior horn cells.

INTERPRETATION

JEV causes an acute flaccid paralysis in children that has similar clinical and pathological features to poliomyelitis. In endemic areas, children with acute flaccid paralysis should be investigated for evidence of JEV infection.

摘要

背景

尽管小儿麻痹症发病率显著下降,但急性弛缓性麻痹在越南儿童中仍然很常见。

方法

1995年期间,越南胡志明市一家转诊中心收治的所有22例急性弛缓性麻痹患儿均接受了病毒培养,并对血清、脑脊液和粪便进行了抗体检测。一年后对这些患儿进行了重新评估并进行了电生理研究。

结果

仅从1例患者的粪便中分离出1型野生脊髓灰质炎病毒,从3例患者中分离出非脊髓灰质炎肠道病毒。22例急性弛缓性麻痹患儿中有12例(55%)有急性日本脑炎病毒(JEV)感染的证据,而88例年龄匹配的医院对照患儿(白喉患儿)中只有1例(1%)有该证据(p<0.0001)。与JEV阴性患儿相比,JEV感染患儿的肌无力起病更快,往往不对称,但累及手臂的可能性较小。所有12例JEV感染患儿在肌无力发作时均发热,7例有急性尿潴留,10例脑脊液有细胞增多。8例JEV阴性患者中有7例符合格林-巴利综合征的病例定义,而12例JEV阳性患儿中只有1例符合。在随访中,JEV感染患儿的残疾程度更高,肌肉萎缩的可能性也比JEV阴性患儿更大。神经传导和肌电图研究表明前角细胞受损。

解读

JEV可导致儿童急性弛缓性麻痹,其临床和病理特征与小儿麻痹症相似。在流行地区,应对急性弛缓性麻痹患儿进行JEV感染证据的调查。

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