Warda Hamza, Alasmar Ola Emad, Wardeh Abdulkareem Muhammad, Ibrahem Ali Mohammad, Alsaadi Esraa, Alsamara Heba, Jouhar Anas
Department of Internal Medecine Homs University Hospital Homs Syria.
Department of Neurology Damascus Hospital Damascus Syria.
Clin Case Rep. 2025 Aug 25;13(9):e70817. doi: 10.1002/ccr3.70817. eCollection 2025 Sep.
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a rare but serious autoimmune disorder that is typically characterized by a broad spectrum of psychiatric and neurological symptoms. In the academic literature, memory deficits often occur alongside psychiatric symptoms, seizures, motor dysfunctions, and other cognitive issues; it is rare to find it dominated by memory impairment with only one previous seizure. We present a unique presentation of anti-NMDAR encephalitis in a 70-year-old Middle Eastern male patient who primarily exhibited memory impairment along with one unrepeated recent seizure. The patient's initial clinical picture did not align with the classic presentation of anti-NMDAR encephalitis, which often includes prominent psychiatric symptoms and neurological features of motor dysfunction. However, brain magnetic resonance imaging (MRI), electroencephalography (EEG), and the presence of anti-NMDAR antibodies in the cerebrospinal fluid support the diagnosis. Physicians should be aware to consider anti-NMDAR encephalitis in patients with memory impairment and a single previous seizure, even in the absence of typical psychiatric or neurological features.
抗N-甲基-D-天冬氨酸受体(NMDAR)脑炎是一种罕见但严重的自身免疫性疾病,其典型特征是具有广泛的精神和神经症状。在学术文献中,记忆缺陷常与精神症状、癫痫发作、运动功能障碍及其他认知问题同时出现;仅有一次既往癫痫发作且以记忆损害为主的情况较为罕见。我们报告了一名70岁中东男性抗NMDAR脑炎患者的独特表现,该患者主要表现为记忆损害以及一次近期未复发的癫痫发作。患者最初的临床表现与抗NMDAR脑炎的经典表现不符,经典表现通常包括突出的精神症状和运动功能障碍的神经学特征。然而,脑磁共振成像(MRI)、脑电图(EEG)以及脑脊液中抗NMDAR抗体的存在支持了诊断。医生应意识到,即使没有典型的精神或神经特征,对于有记忆损害和一次既往癫痫发作的患者也应考虑抗NMDAR脑炎。