Balamuthia mandrillaris amoebic encephalitis mimicking tuberculous meningitis.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Neuropathology Pub Date : 2024-02-01 Epub Date: 2023-06-28 DOI:10.1111/neup.12932
Yoya Ono, Kazuhiro Higashida, Kanako Yamanouchi, Shusuke Nomura, Yuki Hanamatsu, Chiemi Saigo, Nobuyuki Tetsuka, Takayoshi Shimohata
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Abstract

A 76-year-old female with no apparent immunosuppressive conditions and no history of exposure to freshwater and international travel presented with headache and nausea 3 weeks before the presentation. On admission, her consciousness was E4V4V6. Cerebrospinal fluid analysis showed pleocytosis with mononuclear cell predominance, elevated protein, and decreased glucose. Despite antibiotic and antiviral therapy, her consciousness and neck stiffness gradually worsened, right eye-movement restriction appeared, and the right direct light reflex became absent. Brain magnetic resonance imaging revealed hydrocephalus in the inferior horn of the left lateral ventricle and meningeal enhancement around the brainstem and cerebellum. Tuberculous meningitis was suspected, and pyrazinamide, ethambutol, rifampicin, isoniazid, and dexamethasone were started. In addition, endoscopic biopsy was performed from the white matter around the inferior horn of the left lateral ventricle to exclude brain tumor. A brain biopsy specimen revealed eosinophilic round cytoplasm with vacuoles around blood vessels, and we diagnosed with amoebic encephalitis. We started azithromycin, flucytosine, rifampicin, and fluconazole, but her symptoms did not improve. She died 42 days after admission. In autopsy, the brain had not retained its structure due to autolysis. Hematoxylin and eosin staining of her brain biopsy specimen showed numerous amoebic cysts in the perivascular brain tissue. Analysis of the 16S ribosomal RNA region of amoebas from brain biopsy and autopsy specimens revealed a sequence consistent with Balamuthia mandrillaris. Amoebic meningoencephalitis can present with features characteristic of tuberculous meningitis, such as cranial nerve palsies, hydrocephalus, and basal meningeal enhancement. Difficulties in diagnosing amoebic meningoencephalitis are attributed to the following factors: (1) excluding tuberculous meningitis by microbial testing is difficult, (2) amoebic meningoencephalitis has low incidence and can occur without obvious exposure history, (3) invasive brain biopsy is essential in diagnosing amoebic meningoencephalitis. We should recognize the possibility of amoebic meningoencephalitis when evidence of tuberculosis meningitis cannot be demonstrated.

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模仿结核性脑膜炎的山魈阿米巴脑炎(Balamuthia mandrillaris amoebic encephalitis)。
一名 76 岁女性,无明显免疫抑制症状,无淡水接触史和国际旅行史,发病前 3 周出现头痛和恶心。入院时,她的意识为 E4V4V6。脑脊液分析显示单核细胞为主的多形核细胞增多,蛋白质升高,葡萄糖降低。尽管接受了抗生素和抗病毒治疗,但她的意识和颈部僵硬逐渐恶化,右眼活动受限,右侧直视光反射消失。脑磁共振成像显示左侧外脑室下角有脑积水,脑干和小脑周围有脑膜强化。医生怀疑是结核性脑膜炎,并开始使用吡嗪酰胺、乙胺丁醇、利福平、异烟肼和地塞米松。此外,为了排除脑肿瘤,还对左侧外脑室下角周围的白质进行了内窥镜活检。脑活检标本显示嗜酸性圆形胞浆,血管周围有空泡,我们诊断为阿米巴脑炎。我们开始使用阿奇霉素、氟尿嘧啶、利福平和氟康唑,但她的症状没有改善。她在入院 42 天后死亡。尸检结果显示,大脑因自溶而未保留其结构。对她的脑活检标本进行苏木精和伊红染色后发现,血管周围的脑组织中有许多阿米巴囊肿。对脑活检标本和尸检标本中阿米巴的 16S 核糖体 RNA 区域进行分析后发现,其序列与山魈巴拉穆氏虫一致。阿米巴脑膜脑炎可表现出结核性脑膜炎的特征,如颅神经麻痹、脑积水和基底脑膜强化。诊断阿米巴脑膜脑炎的困难可归因于以下因素:(1)很难通过微生物检测排除结核性脑膜炎;(2)阿米巴脑膜脑炎发病率低,可在无明显接触史的情况下发生;(3)侵入性脑活检对诊断阿米巴脑膜脑炎至关重要。在无法证明结核性脑膜炎的证据时,我们应认识到阿米巴脑膜脑炎的可能性。
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来源期刊
Neuropathology
Neuropathology 医学-病理学
CiteScore
4.10
自引率
4.30%
发文量
105
审稿时长
6-12 weeks
期刊介绍: Neuropathology is an international journal sponsored by the Japanese Society of Neuropathology and publishes peer-reviewed original papers dealing with all aspects of human and experimental neuropathology and related fields of research. The Journal aims to promote the international exchange of results and encourages authors from all countries to submit papers in the following categories: Original Articles, Case Reports, Short Communications, Occasional Reviews, Editorials and Letters to the Editor. All articles are peer-reviewed by at least two researchers expert in the field of the submitted paper.
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