[1例人类免疫缺陷病毒患者的视神经脊髓炎谱系障碍]。

Erika Elizabeth González-Sansores, Brenda Bertado-Cortés, Daniela Alexia León-Castillo, Nallely Rubalcava-Sánchez
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引用次数: 0

摘要

背景:视神经脊髓炎(NMO)是一种以视神经和脊髓为优先靶点的自身免疫性疾病。虽然HIV感染也可引起神经炎和脊髓炎,但HIV与NMO相关的实体最近已被阐明,然而,对这种疾病的背景知之甚少。目的:描述1例hiv阳性并发抗aqp4抗体阳性的纵向广泛横断面脊髓炎(LETM)患者的临床特征、影像学、治疗和功能预后。临床病例:36岁男性,2017年确诊为HIV病史,正在接受抗逆转录病毒治疗。2021年3月,患者因完全性脊髓综合征入院接受研究,MRI证实T8-L1纵向广泛病变,CSF与AQP4血清阳性,根据Wingerchuk标准合并NMO诊断,开始使用利妥昔单抗,症状改善,扩展残疾状态量表(EDSS)从4到1客观化。结论:与HIV相关的NMO实体是罕见的,这种现象通常发生在诊断时或免疫系统开始治疗后,此时免疫系统仍然能够产生夸大的免疫反应,然而,我们报道的病例中,NMO首次出现在诊断后3年,与之前报道的病例相比,因此我们认为可能涉及其他机制,例如B细胞调节的改变和直接的病毒作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[Neuromyelitis optica spectrum disorder in a patient with human immunodeficiency virus].

[Neuromyelitis optica spectrum disorder in a patient with human immunodeficiency virus].

[Neuromyelitis optica spectrum disorder in a patient with human immunodeficiency virus].

[Neuromyelitis optica spectrum disorder in a patient with human immunodeficiency virus].

Background: Neuromyelitis optica spectrum (NMO) is an autoimmune condition with preferential target at the optic nerves and spinal cord. Although HIV infection can also cause neuritis and myelitis, the entity of HIV related to NMO has recently been elucidated, however, little is known about the context of this disease. Objective: To describe the clinical characteristics, imaging, treatment, and functional prognosis in an HIV-positive patient who developed an episode of longitudinally extensive transverse myelitis (LETM) with positive anti-AQP4 antibodies.

Clinic case: 36-year-old man with a history of HIV diagnosed in 2017, on antiretroviral treatment. On March 2021 he was admitted for study due to complete spinal cord syndrome, corroborating in MRI a longitudinally extensive lesion from T8-L1, with CSF with and AQP4 seropositivity, a diagnosis of NMO was integrated by Wingerchuk criteria and rituximab is started with symptomatic improvement, objectifying it with the Expanded Disability Status Scale (EDSS) from 4 to 1.

Conclusion: NMO entity related to HIV is rare, this phenomenon being classically found at the time of diagnosis or after the start of treatment when the immune system is still capable of developing an exaggerated immune response, however in the case we report the debut of NMO occurred 3 years after diagnosis, contrasting with previously reported cases, so we suggest that some other mechanisms could be involved, such as altered regulation of B cells and a direct viral effect.

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