Häusler Martin, Ramaekers Vincent Thomas, Doenges Martin, Schweizer Klaus, Ritter Klaus, Schaade Lars
Department of Paediatrics, Division of Paediatric Neurology, University Hospital, RWTH Aachen, Germany.
J Med Virol. 2002 Oct;68(2):253-63. doi: 10.1002/jmv.10201.
Neurological complications of Epstein-Barr virus (EBV) have been reported almost exclusively in the course of acute primary infections. The role of EBV in paediatric neurological disease was investigated prospectively over a 2-year period, searching for acute primary, chronic, and reactivated EBV infections. Active EBV infections were diagnosed in 10/48 patients, including two with acute primary EBV infections (cranial neuritis and cerebellitis), one with chronic active infection (T/NK cell lymphoma with cranial neuritis), and seven with reactivated infections. Among these seven patients, three showed "Alice in Wonderland" syndrome, one facial nerve palsy, one progressive macrocephaly, and two prolonged encephalitic illness. The prognosis was good except for the patient with lethal T/NK cell lymphoma and the two girls with encephalitic illness. Despite steroid treatment, these girls suffered prolonged cognitive impairment and epileptic seizures. Both developed left-sided hippocampal atrophy, and one of them hippocampal sclerosis. Like primary infections, reactivated EBV infections cause neurological complications in a considerable number of paediatric patients, lead to serious long-term complications, and may contribute to the pathogenesis of hippocampal lesions.
几乎仅在急性原发性感染过程中报告过爱泼斯坦-巴尔病毒(EBV)的神经系统并发症。在为期2年的时间里,对EBV在儿童神经系统疾病中的作用进行了前瞻性研究,以寻找急性原发性、慢性和再激活的EBV感染。48例患者中有10例诊断为活动性EBV感染,其中2例为急性原发性EBV感染(颅神经炎和小脑炎),1例为慢性活动性感染(伴有颅神经炎的T/NK细胞淋巴瘤),7例为再激活感染。在这7例患者中,3例表现为“爱丽丝梦游仙境”综合征,1例面神经麻痹,1例进行性巨头畸形,2例为迁延性脑炎。除了患有致命性T/NK细胞淋巴瘤的患者以及2例患有脑炎的女孩外,预后良好。尽管接受了类固醇治疗,这两名女孩仍遭受了长期的认知障碍和癫痫发作。两人均出现左侧海马萎缩,其中一人出现海马硬化。与原发性感染一样,再激活的EBV感染在相当数量的儿科患者中会引起神经系统并发症,导致严重的长期并发症,并可能促成海马病变的发病机制。