头脑风暴一个肉芽肿性脑炎病例

Patrick Benoit, Stephanie Wang, Catherine Wang, Arpita Chakravarti, Julian A Villalba, I. Ali, Shantanu Roy, Sarah GH Sapp, Sarah Reagan-Steiner, Kristoff Nelson, Romain Cayrol, Me-Linh Luong, Sophie Grand'Maison, Michaël Desjardins
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引用次数: 0

摘要

自由生活阿米巴(FLA)可引起严重和致命的中枢神经系统感染,但很难诊断。本病例是一名 74 岁免疫功能正常的妇女,因局灶性神经症状和右侧小脑半球强化病变入院。首次脑活检显示有肉芽肿性炎症,但未发现微生物。经过短暂的临床改善后,她的病情最终在初次就诊 4 个月后恶化,核磁共振检查证实她的所有脑叶都出现了多个新的肿块。第二次脑活检发现了肉芽肿性急性炎症,病原体含有一个大的中央核,核仁突出,与自由生活的阿米巴一致。疾病预防控制中心进行的免疫组化和聚合酶链反应检测对阿卡阿米巴属呈阳性反应,确诊为阿卡阿米巴属引起的肉芽肿阿米巴脑炎(GAE)。经组织病理学复查,通过组织化学和免疫组化方法在第一次脑活检中发现了阿米巴囊肿和滋养体。由于 FLA 感染发病率低、临床和影像学表现无特异性、缺乏可用的诊断工具以及临床医生的不熟悉,因此其诊断具有挑战性。本病例强调了将 FLA 识别为肉芽肿性脑炎潜在病因的重要性,即使在没有危险因素的情况下也是如此,因为在病例报告中,早期治疗可能会带来良好的结果。如果怀疑是FLA,疾病预防控制中心实验室会及时提供确诊检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brainstorm: A case of granulomatous encephalitis
Free-living amoebas (FLA) can cause severe and fatal central nervous system infections that are difficult to diagnose. We present the case of a 74-year-old immunocompetent woman admitted for focal neurological symptoms with enhancing lesions in the right cerebellar hemisphere. A first cerebral biopsy showed granulomatous inflammation, but no microorganisms were identified. After transient clinical improvement, she eventually deteriorated 4 months after initial presentation, with an MRI confirming multiple new masses affecting all cerebral lobes. A second brain biopsy revealed granulomatous and acute inflammation with organisms containing a large central nucleus with prominent karyosome, consistent with free-living amoebas. Immunohistochemical and polymerase chain reaction assays performed at CDC were positive for Acanthamoeba spp., confirming the diagnosis of granulomatous amoebic encephalitis (GAE) caused by Acanthamoeba spp. The patient was treated with combination therapy recommended by CDC, but unfortunately died a few days later. Upon histopathological rereview, amoebic cysts and trophozoites were identified by histochemical and immunohistochemical methods in the first cerebral biopsy. FLA infections can be challenging to diagnose because of the low incidence, the non-specific clinical and radiological presentation, the lack of accessible diagnostic tools, and clinicians’ unfamiliarity. This case highlights the importance of recognizing FLA as a potential cause of granulomatous encephalitis, even in the absence of risk factors, as early treatment might be associated with favorable outcomes in case reports. When suspected, CDC laboratories offer tests to confirm the diagnosis promptly.
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