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[一例合并骨髓增生异常综合征(MDS)的慢性疱疹性脑炎]

[A case of chronic herpes encephalitis with myelodysplastic syndrome (MDS)].

作者信息

Ejima M, Tanaka H, Ueda M, Ota K, Maruyama S

机构信息

Department of Neurology, Tokyo Women's Medical College.

出版信息

Rinsho Shinkeigaku. 1994 Mar;34(3):246-9.

PMID:8200142
Abstract

A 72-year-old male suffering with MDS was admitted to our hospital because of slowly progressive dementia, convulsions and consciousness disturbance. A CT scan of the brain showed a low density area in the right temporal to parietal lobe and T2-weighted MRI of the brain revealed a high intensity signal in the same area. Herpes simplex virus DNA was detected in CSF by PCR method. He was diagnosed as having herpes simplex encephalitis but his clinical course was prolonged and considered atypical as herpetic infection in CNS. However, after administration of aciclovir, progression of his symptoms stopped, and a CT scan still revealed abnormal findings with the same area after more than four months. We thought his chronic course of herpes encephalitis was caused by incomplete immune function suppressed by MDS.

摘要

一名72岁患有骨髓增生异常综合征的男性因缓慢进展的痴呆、惊厥和意识障碍入住我院。脑部CT扫描显示右侧颞叶至顶叶有低密度区,脑部T2加权磁共振成像显示同一区域有高强度信号。通过聚合酶链反应(PCR)方法在脑脊液中检测到单纯疱疹病毒DNA。他被诊断为患有单纯疱疹性脑炎,但其临床病程延长,被认为是中枢神经系统疱疹感染的非典型病例。然而,给予阿昔洛韦治疗后,他的症状进展停止,四个多月后CT扫描仍显示同一区域有异常表现。我们认为他的疱疹性脑炎慢性病程是由骨髓增生异常综合征抑制的不完全免疫功能所致。

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