Influenza virus-induced encephalopathy: Clinicopathologic study of an autopsied case

被引:67
作者
Takahashi, M
Yamada, T
Nakashita, Y
Saikusa, H
Deguchi, M
Kida, H
Tashiro, M
Toyoda, T
机构
[1] Fukuoka Univ, Sch Med, Dept Internal Med & Hlth Care, Jonan Ku, Fukuoka 8140180, Japan
[2] Sasebo Municipal Gen Hosp, Dept Pediat, Sapporo, Hokkaido, Japan
[3] Saikusu Pediat Clin, Sasebo, Japan
[4] Deguchi Pediat Clin, Nagasaki, Japan
[5] Hokkaido Univ, Grad Sch Vet Med, Sapporo, Hokkaido, Japan
[6] Natl Inst Infect Dis, Dept Viral Dis & Vaccine Control, Tokyo, Japan
[7] Kurume Univ, Sch Med, Dept Virol, Fukuoka, Japan
关键词
autopsy; encephalopathy; immunohistochemistry; influenza A virus; reverse transcriptase polymerase chain reaction; viremia;
D O I
10.1046/j.1442-200x.2000.01203.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Rapid progressive encephalopathy with a high fever, consciousness loss and recurrent convulsions has been occasionally reported in children during influenza pandemics in Japan since 1995. We examined a 2-year old girl with hemorrhagic shock and encephalopathy syndrome associated with acute influenza A virus infection (A/Nagasaki/76/98; H3N2), to answer several questions for which no histologic or virologic data exist. Methods: A clinicopathologic study using immunohistochemical staining and viral genome detection by reverse transcriptase polymerase chain reaction (RT-PCR) was performed with this autopsied case. Results: The virus antigen was positive in CD8(+) T lymphocytes from the lung and spleen. The virus infected a very limited part of the brain, especially Purkinje cells in the cerebellum and many neurons in the pons, without inducing an overt immunologic reaction from the host. The RT-PCR used for detecting the hemagglutinin gene demonstrated positive bands in all frozen tissues and cerebrospinal fluid taken at autopsy and not in samples obtained on admission. Conclusions: The pathologic change induced by the direct viral invasion cannot be responsible for all of the symptoms, especially for the rapid and severe clinical course of the disease within 24-48 h after the initial respiratory symptoms. Together with the rapid production of several inflammatory cytokines, the breakdown of the blood-brain barrier may induce severe brain edema and can be a major pathologic change for the disease. Any therapeutic strategy to control this multistep progression of the disease could be effective.
引用
收藏
页码:204 / 214
页数:11
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