Department of Neurology, Perelman School of Medicine, PCAM 765 South Tower, University of Pennsylvania, 3400 Convention Avenue, Philadelphia, PA, 19104, USA.
J Neurovirol. 2022 Dec;28(4-6):467-472. doi: 10.1007/s13365-022-01096-x. Epub 2022 Sep 13.
The report of death of a person from amebic meningoencephalitis, the proverbial "brain-eating ameba," Naegleria fowleri, acquired in a state park lake in Iowa in July 2022 has once again raised the seasonal alarms about this pathogen. While exceptionally rare, its nearly universal fatality rate has panicked the public and made for good copy for the news media. This review will address free-living ameba that have been identified as causing CNS invasion in man, namely, Naegleria fowleri, Acanthamoeba species, Balamuthia mandrillaris, and Sappinia diploidea (Table 1). Of note, several Acanthamoeba spp. and Balamuthia mandrillaris may also be associated with localized extra-CNS infections in individuals who are immunocompetent and disseminated disease in immunocompromised hosts. These ameba are unique from other protozoa in that they are free-living, have no known insect vector, do not result in a human carrier state, and are typically unassociated with poor sanitation. Table 1 Free-living ameba that have been identified as causing CNS invasion in man, namely, Naegleria fowleri, Acanthamoeba species, Balamuthia mandrillaris, and Sappinia diploidea Entity Pathogenic ameba Predisposing disorders Portal of entry Incubation period Clinical features Radiographic findings CSF finding Diagnostic measures Primary amebic meningoencephalitis Naegleria fowleri; N. australiensis; N. italica Previously healthy children or young adults Olfactory epithelium 2-14 days (average 5 days) Headache, fever, altered mental status, meningeal signs; seizures Brain edema; meningeal enhancement; hydrocephalus; basal ganglia infarctions Increased opening pressure; neutrophilic pleocytosis (~ 1000 cells/cu mm); low glucose Brain biopsy, CSF wet prep, IIF culture or PCR Granulomatous amebic encephalitis Acanthamoeba spp.; Balamuthia mandrillaris; Sappinia diploidea Typically, immunocompromised individual Skin sinuses; olfactory epithelium respiratory tract Weeks to months Headache; altered mental status seizures, focal neurological findings Focal parenchymal lesions with edema; hemorrhagic infarctions; meningeal enhancement Generally, LP contraindicated; when performed lymphocytic pleocytosis; increased protein; low glucose Brain biopsy, CSF culture, wet prep, IIF, or PCR IIF indirect immunofluorescence, LP lumbar puncture, PCR polymerase chain reaction.
2022 年 7 月,爱荷华州一个州立公园的湖泊中,一名男子死于阿米巴脑膜脑炎(俗称“食脑变形虫”),这种疾病再次引发了人们对这种病原体的季节性警惕。尽管这种疾病极其罕见,但它近乎百分之百的致死率令公众感到恐慌,也成为新闻媒体的热门素材。本综述将介绍已确定可引起人类中枢神经系统(CNS)侵袭的自由生活阿米巴,即福氏耐格里变形虫、棘阿米巴属物种、曼氏利什曼原虫和双房 diploidea(表 1)。值得注意的是,几种棘阿米巴属物种和曼氏利什曼原虫也可能与免疫功能正常个体的局部中枢神经系统外感染以及免疫功能低下宿主的播散性疾病有关。与其他原生动物不同,这些阿米巴是自由生活的,没有已知的昆虫媒介,不会导致人类带菌状态,通常与卫生条件差无关。表 1 已确定可引起人类中枢神经系统(CNS)侵袭的自由生活阿米巴,即福氏耐格里变形虫、棘阿米巴属物种、曼氏利什曼原虫和双房 diploidea
实体
致病阿米巴
易患疾病
门户入口
潜伏期
临床特征
影像学表现
CSF 发现
诊断措施
原发性阿米巴脑膜脑炎
福氏耐格里变形虫;N. australiensis;N. italica
既往健康的儿童或年轻人
嗅觉上皮
2-14 天(平均 5 天)
头痛、发热、精神状态改变、脑膜刺激征;癫痫发作
脑水肿;脑膜增强;脑积水;基底节梗死
颅内压升高;中性粒细胞增多(~1000 个/立方毫米);低糖
脑活检、CSF 湿片、IIF 培养或 PCR
肉芽肿性阿米巴脑炎
棘阿米巴属物种;曼氏利什曼原虫;双房 diploidea
通常为免疫功能低下的个体
皮肤窦;嗅觉上皮呼吸道
数周至数月
头痛;精神状态改变;癫痫发作;局灶性神经功能障碍
有水肿的局灶性实质病变;出血性梗死;脑膜增强
通常禁忌 LP;当进行 LP 时,淋巴细胞增多;蛋白增加;低糖
脑活检、CSF 培养、湿片、IIF 或 PCR
IIF 间接免疫荧光、LP 腰椎穿刺、PCR 聚合酶链反应。