免疫功能正常儿童中枢神经系统血管炎一例报告。

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
John Paul Aboubechara, Trishna Kantamneni, Katrina Pasao
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引用次数: 0

摘要

阿米巴肉芽肿性脑炎是一种罕见的疾病,具有很高的死亡率。诊断和治疗的延误是常见的,因为除了它的非特异性临床表现,对有机体的信息有限。先前的报告表明,脑炎表现为整个中枢神经系统的多灶性病变,伴增强和水肿。在这里,我们报告了一例4岁的健康女童,她出现了一种新的mandrillaris感染的病理表现,包括血管炎,包括多根颅内大血管以及多根脑神经的炎症。尽管早期诊断和开始有针对性的治疗,感染最终是致命的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Balamuthia Mandrillaris Central Nervous System Vasculitis in an Immunocompetent Child: Case Report.

Balamuthia mandrillaris granulomatous amebic encephalitis is a rare disease that is associated with a high rate of mortality. Delays in diagnosis and treatment are common because of limited information on the organism in addition to its nonspecific clinical presentation. Prior reports have demonstrated that the encephalitis presents as multifocal lesions throughout the central nervous system with enhancement and edema. Here we report a case involving a 4-year-old previously healthy female child with a novel pathologic presentation of B mandrillaris infection, including vasculitis involving multiple large intracranial vessels as well as inflammation of multiple cranial nerves. The infection was ultimately fatal despite early diagnosis and initiation of targeted treatment.

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来源期刊
Journal of Child Neurology
Journal of Child Neurology 医学-临床神经学
CiteScore
4.20
自引率
5.30%
发文量
111
审稿时长
3-6 weeks
期刊介绍: The Journal of Child Neurology (JCN) embraces peer-reviewed clinical and investigative studies from a wide-variety of neuroscience disciplines. Focusing on the needs of neurologic patients from birth to age 18 years, JCN covers topics ranging from assessment of new and changing therapies and procedures; diagnosis, evaluation, and management of neurologic, neuropsychiatric, and neurodevelopmental disorders; and pathophysiology of central nervous system diseases.
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