Frank Y, Lim W, Kahn E, Farmer P, Gorey M, Pahwa S
Department of Neurology, North Shore University Hospital, Manhasset, NY 11030.
Pediatr Neurol. 1989 Jan-Feb;5(1):64-7. doi: 10.1016/0887-8994(89)90013-1.
A 4 1/2-year-old girl with acquired immunodeficiency syndrome and prolonged varicella zoster virus skin infection developed multiple ischemic strokes and radiologic and histopathologic evidence of central nervous system vasculitis. Typical features of acquired immunodeficiency syndrome encephalitis were not present and there was no evidence of vasculitis outside the nervous system. Central nervous system vasculitis probably resulted from varicella zoster virus infection that persisted because of immunodeficiency. This acquired immunodeficiency syndrome complication has only rarely been described in adults and to our knowledge has not been described in children.
一名4岁半患获得性免疫缺陷综合征且水痘带状疱疹病毒皮肤感染迁延不愈的女孩发生了多发性缺血性中风,并有中枢神经系统血管炎的影像学和组织病理学证据。未出现获得性免疫缺陷综合征脑炎的典型特征,且神经系统外无血管炎证据。中枢神经系统血管炎可能是由因免疫缺陷而持续存在的水痘带状疱疹病毒感染所致。这种获得性免疫缺陷综合征并发症在成人中鲜有报道,据我们所知,在儿童中尚未见报道。