{"title":"抗nmda - r脑炎1例。","authors":"Bünyamin Tosunoğlu, Hafize Nalan Güneş, Hatice Mediha Kına, Burcu Gökçe Çokal","doi":"10.5114/ppn.2022.120492","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Anti-N-methyl-D-aspartate receptor encephalitis (NMDA-R) is the most common among autoimmune encephalitis caused by antibodies developed against surface antigens. It was first identified in 2007 as presenting with seizures, autonomic dysfunction and movement disorders, in addition to acute or subacute onset of neuropsychiatric symptoms. Multifocal, nonspecific white matter lesions can be seen on cranial magnetic resonance imaging (MRI). Since paraneoplasia is usually found in the etiology, malignancy should be screened in patients with NMDA-R encephalitis.</p><p><strong>Case description: </strong>In our case, a 48-year-old patient is presented who has been diagnosed with anti-NMDA-R encephalitis during the examinations, complaining of numbness on the left side of his face, seizures, imbalance, excessive talkativeness and insomnia.</p><p><strong>Comment: </strong>Autoimmune encephalitis should be considered in patients with suspected autoimmune encephalitis, which takes severe clinical course and fails to respond to treatment adequately; NMDA receptor antibodies and other autoantibody tests should be requested, malignancy screening should be performed and treatment should be started in the early period.</p>","PeriodicalId":74481,"journal":{"name":"Postepy psychiatrii neurologii","volume":"31 3","pages":"138-140"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/cf/c4/PPN-31-48031.PMC9946364.pdf","citationCount":"0","resultStr":"{\"title\":\"ANTI-NMDA-R encephalitis: case report.\",\"authors\":\"Bünyamin Tosunoğlu, Hafize Nalan Güneş, Hatice Mediha Kına, Burcu Gökçe Çokal\",\"doi\":\"10.5114/ppn.2022.120492\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Anti-N-methyl-D-aspartate receptor encephalitis (NMDA-R) is the most common among autoimmune encephalitis caused by antibodies developed against surface antigens. It was first identified in 2007 as presenting with seizures, autonomic dysfunction and movement disorders, in addition to acute or subacute onset of neuropsychiatric symptoms. Multifocal, nonspecific white matter lesions can be seen on cranial magnetic resonance imaging (MRI). Since paraneoplasia is usually found in the etiology, malignancy should be screened in patients with NMDA-R encephalitis.</p><p><strong>Case description: </strong>In our case, a 48-year-old patient is presented who has been diagnosed with anti-NMDA-R encephalitis during the examinations, complaining of numbness on the left side of his face, seizures, imbalance, excessive talkativeness and insomnia.</p><p><strong>Comment: </strong>Autoimmune encephalitis should be considered in patients with suspected autoimmune encephalitis, which takes severe clinical course and fails to respond to treatment adequately; NMDA receptor antibodies and other autoantibody tests should be requested, malignancy screening should be performed and treatment should be started in the early period.</p>\",\"PeriodicalId\":74481,\"journal\":{\"name\":\"Postepy psychiatrii neurologii\",\"volume\":\"31 3\",\"pages\":\"138-140\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/cf/c4/PPN-31-48031.PMC9946364.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Postepy psychiatrii neurologii\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5114/ppn.2022.120492\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Postepy psychiatrii neurologii","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5114/ppn.2022.120492","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目的:抗n -甲基- d -天冬氨酸受体脑炎(NMDA-R)是由针对表面抗原产生的抗体引起的自身免疫性脑炎中最常见的。2007年首次发现,除了急性或亚急性发作的神经精神症状外,还表现为癫痫发作、自主神经功能障碍和运动障碍。头颅磁共振成像(MRI)显示多灶性、非特异性白质病变。由于在病因学上通常发现副瘤,因此NMDA-R脑炎患者应筛查恶性肿瘤。病例描述:我们的病例是一名48岁的患者,在检查中被诊断为抗nmda - r脑炎,主诉为左脸麻木,癫痫发作,失衡,多话和失眠。评论:疑似自身免疫性脑炎患者,临床病程严重且治疗效果不佳,应考虑自身免疫性脑炎;应要求进行NMDA受体抗体和其他自身抗体检测,进行恶性肿瘤筛查,并在早期开始治疗。
Purpose: Anti-N-methyl-D-aspartate receptor encephalitis (NMDA-R) is the most common among autoimmune encephalitis caused by antibodies developed against surface antigens. It was first identified in 2007 as presenting with seizures, autonomic dysfunction and movement disorders, in addition to acute or subacute onset of neuropsychiatric symptoms. Multifocal, nonspecific white matter lesions can be seen on cranial magnetic resonance imaging (MRI). Since paraneoplasia is usually found in the etiology, malignancy should be screened in patients with NMDA-R encephalitis.
Case description: In our case, a 48-year-old patient is presented who has been diagnosed with anti-NMDA-R encephalitis during the examinations, complaining of numbness on the left side of his face, seizures, imbalance, excessive talkativeness and insomnia.
Comment: Autoimmune encephalitis should be considered in patients with suspected autoimmune encephalitis, which takes severe clinical course and fails to respond to treatment adequately; NMDA receptor antibodies and other autoantibody tests should be requested, malignancy screening should be performed and treatment should be started in the early period.