Asenbauer B, McEntagart M, King M D, Gallagher P, Burke M, Farrell M A
Department of Neurology, Children's Hospital, Dublin, Ireland.
Neuropediatrics. 1998 Jun;29(3):120-3. doi: 10.1055/s-2007-973546.
Acute herpes simplex encephalitis (HSE) carries significant morbidity and mortality even after early treatment with antiviral agents (7). As well as causing acute neurological disease, Herpes viruses are associated with relapsing--remitting (Varicella--Zoster, Epstein-Barr) and chronic (Rasmussen encephalitis) disease processes (1). A two-year-old girl developed acute HSE which was followed by a 10-year neurologic illness characterised by asymmetric spastic tetraparesis, pseudobulbar palsy, the opercular syndrome of Foix-Chavany-Marie (4) and seizures. The neurological signs remained static until the child died suddenly 12 years after disease onset. Neuropathologic examination demonstrated active chronic encephalitis. Herpes simplex virus (HSV) DNA was recovered from formalin-fixed paraffin-embedded brain tissue. This case provides additional evidence for the development of chronic neurological disease attributable to persistence of herpes simplex virus type 1.
急性单纯疱疹病毒性脑炎(HSE)即便在早期使用抗病毒药物治疗后,仍具有较高的发病率和死亡率(7)。疱疹病毒除了会引发急性神经疾病外,还与复发-缓解型(水痘-带状疱疹病毒、EB病毒)和慢性(拉斯穆森脑炎)疾病进程相关(1)。一名两岁女童患上急性HSE,随后出现了长达10年的神经疾病,其特征为不对称性痉挛性四肢瘫、假性延髓麻痹、福-恰-马氏盖部综合征(4)以及癫痫发作。神经体征一直未变,直至患儿在疾病发作12年后突然死亡。神经病理学检查显示为活动性慢性脑炎。从福尔马林固定石蜡包埋的脑组织中检测到单纯疱疹病毒(HSV)DNA。该病例为1型单纯疱疹病毒持续存在导致慢性神经疾病的发生提供了更多证据。