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伴有基底节和广泛白质受累的单纯疱疹病毒性脑炎的不寻常病程。

Unusual progression of herpes simplex encephalitis with basal ganglia and extensive white matter involvement.

作者信息

Ono Yoichi, Manabe Yasuhiro, Nishimura Hirotake, Kono Syoichiro, Narai Hisashi, Omori Nobuhiko, Nanba Yoichiro, Abe Koji

机构信息

Department of Neurology and.

出版信息

Neurol Int. 2009 Nov 16;1(1):e9. doi: 10.4081/ni.2009.e9.

Abstract

We report a 51-year old male with herpes simplex encephalitis (HSE) showing unusual progression and magnetic resonance (MR) findings. The initial neurological manifestation of intractable focal seizure with low-grade fever persisted for three days, and rapidly coma, myoclonic status, and respiratory failure with high-grade fever emerged thereafter. The polymerase chain reaction (PCR) result of cerebrospinal fluid (CSF) was positive for HSV-1 DNA. In the early stage, MR images (MRI) were normal. On subsequent MR diffusion-weighted (DW) and fluid-attenuated inversion recovery (FLAIR) images, high-intensity areas first appeared in the left frontal cortex, which was purely extra-temporal involvement, and extended into the basal ganglia, then the white matter, which are relatively spared in HSE. Antiviral therapy and immunosuppressive therapy did not suppress the progression of HSE, and finally severe cerebral edema developed into cerebral herniation, which required emergency decompressive craniectomy. Histological examination of a biopsy specimen of the white matter detected perivascular infiltration and destruction of basic structure, which confirmed non specific inflammatory change without obvious edema or demyelination. The present case shows both MR and pathological findings in the white matter in the acute stage of HSE.

摘要

我们报告了一例51岁男性单纯疱疹病毒性脑炎(HSE)患者,其病情进展及磁共振成像(MR)表现均不寻常。最初的神经系统表现为伴有低热的顽固性局灶性癫痫发作,持续三天,随后迅速出现昏迷、肌阵挛状态及伴有高热的呼吸衰竭。脑脊液(CSF)聚合酶链反应(PCR)结果显示HSV-1 DNA呈阳性。早期,磁共振成像(MRI)正常。随后的磁共振扩散加权成像(DW)和液体衰减反转恢复序列(FLAIR)图像显示,高强度区域最初出现在左侧额叶皮质,这是单纯的颞叶外受累,随后扩展至基底节,然后是白质,而在HSE中白质相对较少受累。抗病毒治疗和免疫抑制治疗未能抑制HSE的进展,最终严重脑水肿发展为脑疝,需要紧急进行减压性颅骨切除术。对白质活检标本进行组织学检查发现血管周围浸润及基本结构破坏,证实为非特异性炎症改变,无明显水肿或脱髓鞘。本病例展示了HSE急性期白质的MR及病理表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1f2/3093220/690d9f3c7df6/ni-2009-1-e9-g001.jpg

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