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Herpes Simplex Encephalitis Akihiko Morita 1 1Department of Internal Medicine, Morita Hospital Keyword: 単純ヘルペス脳炎 , アシクロビル , 再発 , 再活性化 , ヘルペス脳炎後自己免疫性脳炎 , herpes simplex encephalitis , HSE , aciclovir , relapse , reactivation , autoimmune encephalitis post-HSE pp.487-494
Published Date 2026/5/1
DOI https://doi.org/10.11477/mf.188160960780050487
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Abstract

Herpes simplex encephalitis (HSE) is the most common cause of sporadic viral encephalitis and is associated with severe mortality and morbidity. No clinical features are pathognomonic for HSE. The gold standard for diagnosing HSE is a herpes simplex virus (HSV) DNA polymerase chain reaction (PCR) test on cerebrospinal fluid (CSF). Treatment with optimal intravenous aciclovir (ACV) can improve outcomes. After the first episode of HSE, neurological relapses or worsening of deficits occur in nearly 30% of patients. If the HSV DNA PCR on CSF is positive, the possibility of ACV-resistant HSE should be considered, and the addition of foscarnet to the ACV treatment may be warranted. If the HSV PCR in CSF is negative, autoimmune encephalitis (AE) post-HSE is considered. All patients with AE post-HSE are tested for one or more neuronal cell-surface and synaptic antibodies, primarily anti-N-methyl-d-aspartate receptor (NMDAR) antibodies, in serum or CSF. The clinical manifestations of AE post-HSE include choreoathetosis and seizures in children, while adults may experience altered consciousness and NMDAR-like symptoms. Most cases of AE post-HSE respond to first-line immunotherapies, which include corticosteroids, intravenous immunoglobulin or plasma exchange. If necessary, treatment can be escalated to second-line immunosuppressants such as rituximab and cyclophosphamide.


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電子版ISSN 1344-8129 印刷版ISSN 1881-6096 医学書院

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