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Mol Neurobiol. 2025 May;62(5):6179-6194. doi: 10.1007/s12035-024-04660-0. Epub 2024 Dec 28.

本文引用的文献

1
Impairment of early neuronal maturation in anti-NMDA-receptor encephalitis.抗 N- 甲基-D-天冬氨酸受体脑炎导致早期神经元成熟障碍。
Psychopharmacology (Berl). 2022 Feb;239(2):525-531. doi: 10.1007/s00213-021-06036-x. Epub 2021 Dec 2.
2
The Association of Ovarian Teratoma and Anti-N-Methyl-D-Aspartate Receptor Encephalitis: An Updated Integrative Review.卵巢畸胎瘤与抗 N-甲基-D-天冬氨酸受体脑炎的关联:一项更新的综合综述。
Int J Mol Sci. 2021 Oct 9;22(20):10911. doi: 10.3390/ijms222010911.
3
Clinical significance of anti-NMDAR concurrent with glial or neuronal surface antibodies.抗 NMDAR 抗体与神经胶质或神经元表面抗体共存的临床意义。
Neurology. 2020 Jun 2;94(22):e2302-e2310. doi: 10.1212/WNL.0000000000009239. Epub 2020 Mar 11.
4
Pregnancy outcomes in anti-NMDA receptor encephalitis: Case series.抗 N- 甲基-D-天冬氨酸受体脑炎的妊娠结局:病例系列。
Neurol Neuroimmunol Neuroinflamm. 2020 Jan 16;7(3). doi: 10.1212/NXI.0000000000000668. Print 2020 May.
5
Catatonia in patients with anti-NMDA receptor encephalitis.抗 NMDA 受体脑炎患者的紧张症。
Psychiatry Clin Neurosci. 2019 Sep;73(9):574-580. doi: 10.1111/pcn.12867. Epub 2019 Jul 1.
6
Glial fibrillary acidic protein immunoglobulin G as biomarker of autoimmune astrocytopathy: Analysis of 102 patients.胶质纤维酸性蛋白免疫球蛋白 G 作为自身免疫性星形胶质细胞病的生物标志物:102 例患者分析。
Ann Neurol. 2017 Feb;81(2):298-309. doi: 10.1002/ana.24881.
7
Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study.抗 NMDA 受体脑炎患者的长期预后的治疗和预后因素:一项观察性队列研究。
Lancet Neurol. 2013 Feb;12(2):157-65. doi: 10.1016/S1474-4422(12)70310-1. Epub 2013 Jan 3.

妊娠期同时出现 NMDA 受体和 GFAP 抗体脑炎。

Concurrent NMDAR and GFAP Antibody Encephalitis During Pregnancy.

机构信息

Neurology Department, SUNY Downstate Health Sciences University, Brooklyn, New York, USA

Neurology Department, SUNY Downstate Health Sciences University, Brooklyn, New York, USA.

出版信息

BMJ Case Rep. 2023 Jul 11;16(7):e250998. doi: 10.1136/bcr-2022-250998.

DOI:10.1136/bcr-2022-250998
PMID:37433686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10347501/
Abstract

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an autoimmune antibody encephalitis, commonly affecting young women with comorbid ovarian teratoma. It typically presents with alteration of consciousness, psychosis, movement disorders eventually deteriorating with seizures, dysautonomia and central hypoventilation requiring critical level of care that may last weeks to months. Removal of teratoma and immunosuppressant therapy support can led to a dramatic recovery.To our knowledge, this is the first illustrated case in the literature of a pregnant woman presenting with concurrent autoimmune NMDAR and anti-glial gibrillary acidic protein(GFAP) antibody encephalitis in the setting of an ovarian teratoma. Despite the teratoma removal and receiving various forms of immunosuppressant therapy, a meaningful neurological improvement was observed following the delivery. After a prolonged hospitalisation and recovery period, the patient and her offspring made an excellent recovery highlighting the significance of early diagnosis and management.

摘要

抗 N-甲基-D-天冬氨酸受体(NMDAR)脑炎是一种自身免疫性抗体脑炎,常见于伴有卵巢畸胎瘤的年轻女性。它通常表现为意识改变、精神病、运动障碍,最终伴有癫痫发作、自主神经功能障碍和中枢性低通气,需要重症监护,持续数周至数月。畸胎瘤切除和免疫抑制剂治疗支持可导致显著恢复。据我们所知,这是文献中首例在卵巢畸胎瘤的背景下,同时发生自身免疫性 NMDAR 和抗神经胶质纤维酸性蛋白(GFAP)抗体脑炎的孕妇病例。尽管切除了畸胎瘤并接受了各种形式的免疫抑制剂治疗,但在分娩后观察到了有意义的神经功能改善。经过长时间的住院和恢复,患者及其后代恢复良好,突出了早期诊断和管理的重要性。