Nagabushana Divya, Nishamol Thavasimuthu, Bhattacharya Kajari, Saini Jitender, Chowdary Ravindranadh, Mahadevan Anita, Polavarapu Kiran, Atchayaram Nalini
Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Department of Neuroimaging and Interventional Neuroradiology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
J Pediatr Neurosci. 2021 Oct-Dec;16(4):327-331. doi: 10.4103/jpn.JPN_225_20. Epub 2022 Jan 7.
Anti-N-methyl-D-aspartate-receptor (A-NMDAR) encephalitis is the most common type of autoimmune encephalitis in the pediatric age group. It is known to be triggered by viral infections such as herpes simplex infections. However, A-NMDAR encephalitis with HIV infection is a very rare event, with cases reported mostly in adults. The current report is of a previously healthy child who presented with recurrent vomiting, irritability, visual impairment, and new onset complex partial seizures and right somatosensory seizures with generalization occurring in clusters. Over a period of 3 weeks, he developed rapidly progressive bilateral painless visual loss, visual hallucinations, and behavioral changes. Brain magnetic resonance imaging (MRI) showed predominantly cortical symmetrical T2/FLAIR hyperintense signal change in parieto-occipito-temporal regions. The serum and cerebrospinal fluid were strongly positive for anti-NMDAR antibodies, and he also tested positive for HIV-1 antibodies acquired by vertical transmission. The patient and mother tested positive for HIV antibodies for the first time. Repeat MRI revealed gliosis in the parieto-occipito-temporal regions, and hippocampi showed volume loss and T2/FLAIR hyperintense signal change in the posterior thalami with patchy hyperintensities in the right putamen. The seizures subsided with immunomodulation along with anti-epileptic drugs, but he had residual cortical visual impairment on follow-up. This is the first report of A-NMDAR encephalitis presenting as a harbinger of HIV infection in a child. This calls for testing for A-NMDAR antibodies in children with HIV infection presenting with neurological or neuropsychiatric manifestations.
抗 N-甲基-D-天冬氨酸受体(A-NMDAR)脑炎是儿童年龄组中最常见的自身免疫性脑炎类型。已知它由病毒感染引发,如单纯疱疹感染。然而,合并 HIV 感染的 A-NMDAR 脑炎是非常罕见的事件,病例大多报道于成人。本报告描述的是一名既往健康的儿童,出现反复呕吐、易激惹、视力障碍,以及新发的复杂部分性发作和右侧躯体感觉发作并成簇出现全身性发作。在 3 周的时间里,他迅速出现双侧无痛性视力进行性减退、视幻觉和行为改变。脑磁共振成像(MRI)显示顶枕颞区主要为皮质对称性 T2/液体衰减反转恢复序列(FLAIR)高信号改变。血清和脑脊液抗 NMDAR 抗体呈强阳性,他还检测出通过垂直传播获得的 HIV-1 抗体阳性。患者及其母亲首次检测出 HIV 抗体阳性。复查 MRI 显示顶枕颞区胶质增生,海马体积缩小,丘脑后部 T2/FLAIR 高信号改变,右侧壳核有斑片状高信号。癫痫发作通过免疫调节联合抗癫痫药物得到控制,但随访时仍有残留的皮质视力障碍。这是首例以 A-NMDAR 脑炎作为儿童 HIV 感染先兆的报告。这提示对于出现神经或神经精神症状的 HIV 感染儿童应检测抗 NMDAR 抗体。