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免疫功能低下者单纯疱疹脑炎的非典型表现和不良预后。

Atypical manifestations and poor outcome of herpes simplex encephalitis in the immunocompromised.

机构信息

Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

出版信息

Neurology. 2012 Nov 20;79(21):2125-32. doi: 10.1212/WNL.0b013e3182752ceb. Epub 2012 Nov 7.

DOI:10.1212/WNL.0b013e3182752ceb
PMID:23136265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3511927/
Abstract

OBJECTIVE

To characterize clinical features, neuroimaging, and outcomes of herpes simplex encephalitis (HSE) in immunocompromised individuals.

METHODS

We performed a retrospective case control review of patients diagnosed with HSE. Adult patients were dichotomized into immunocompromised (n = 14) and immunocompetent groups (n = 15).

RESULTS

Fewer immunocompromised patients presented with prodromal symptoms and focal deficits. While the majority of CSF profiles in the immunocompromised patients were mononuclear cells predominant, 3 had polymorphonuclear predominance and another 3 had normal profiles. MRI showed widespread cortical involvement, with brainstem or cerebellar involvement in some. Two immunocompromised patients had recurrent HSE. The immunosuppressed state was associated with a decrease in Karnofsky Performance Status Scale (KPSS) score of 23.1 (p = 0.018). Every 1-day delay in initiation of acyclovir was associated with a decrease in KPSS of 10.2 (p = 0.002), and every 10 cell/mm(3) increase of CSF leukocytosis was associated with an increase in KPSS of 0.7 (p = 0.009). Mortality rate was 6 times higher in the immunocompromised patients.

CONCLUSIONS

Immunocompromised states may predispose to HSE with atypical clinical and neuroradiologic features. Immunocompromised individuals with HSE have significantly worse outcomes and mortality. Early diagnosis and treatment is associated with improved outcome. The findings are particularly important in light of the increasing use of potent immunosuppressive and immunomodulatory therapies.

摘要

目的

描述免疫抑制个体单纯疱疹脑炎(HSE)的临床特征、神经影像学表现和转归。

方法

我们对诊断为 HSE 的患者进行了回顾性病例对照研究。将成年患者分为免疫抑制组(n=14)和免疫正常组(n=15)。

结果

免疫抑制组患者前驱症状和局灶性缺损较少。虽然免疫抑制组患者的大多数脑脊液表现为单核细胞为主,但有 3 例以多形核细胞为主,另有 3 例表现正常。MRI 显示广泛的皮质受累,部分患者伴有脑干或小脑受累。2 例免疫抑制患者出现复发性 HSE。免疫抑制状态与 Karnofsky 表现状态评分(KPSS)降低 23.1 分有关(p=0.018)。阿昔洛韦起始治疗每延迟 1 天,KPSS 降低 10.2 分(p=0.002),CSF 白细胞增多每增加 10 个/mm(3),KPSS 增加 0.7 分(p=0.009)。免疫抑制患者的死亡率高 6 倍。

结论

免疫抑制状态可能使 HSE 具有不典型的临床和神经影像学特征。免疫抑制的 HSE 患者预后和死亡率显著更差。早期诊断和治疗与改善预后相关。鉴于越来越多地使用强效免疫抑制和免疫调节治疗,这些发现尤为重要。

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