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抗N-甲基-D-天冬氨酸受体脑炎与危及生命的窦房结功能障碍:一例报告、文献综述及23例病例分析

Anti-N-Methyl-D-Aspartate Receptor Encephalitis and Life-Threatening Sinus Node Dysfunction: A Case Report, Literature Review, and Analysis of 23 Cases.

作者信息

Khachatryan Aleksan, Tamazyan Vahagn, Sargsyan Margarita, Harutyunyan Hakob, Alejandro Joel, Batikyan Ashot

机构信息

Department of Internal Medicine, University of Maryland Medical Center, Midtown Campus, Baltimore, USA.

Department of Internal Medicine, Maimonides Medical Center, New York, USA.

出版信息

Cureus. 2024 Jul 13;16(7):e64472. doi: 10.7759/cureus.64472. eCollection 2024 Jul.

DOI:10.7759/cureus.64472
PMID:39135820
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11318722/
Abstract

Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is the most common form of autoimmune encephalitis, presenting with various psychiatric manifestations, including behavioral and cognitive impairments, movement disorders, decreased consciousness, dysphasia, seizures, and autonomic dysfunction. Autonomic dysfunction may involve hyperthermia, apnea, hypotension, tachycardia, and life-threatening manifestations of sinus node dysfunction (SND), such as bradycardia, sinus pause or arrest, and asystole. The severity and significance of SND are critical, as it is not uncommon for these patients to progress into asystolic cardiac arrest, potentially contributing to morbidity and mortality. Accordingly, we present the case of an 18-year-old female with anti-NMDAR encephalitis who experienced multiple episodes of sinus pause/arrest and asystolic cardiac arrest, achieving a return of spontaneous circulation after successful CPR in all instances, ultimately requiring permanent pacemaker implantation. Additionally, we performed a literature review and analyzed 23 similar anti-NMDAR encephalitis cases with SND manifestations, including sinus pause/arrest or asystolic cardiac arrest, to identify common risk factors and describe management strategies and outcomes. Moreover, we investigated the potential association between teratoma and permanent pacemaker use in SND.

摘要

抗 N-甲基-D-天冬氨酸受体(抗 NMDAR)脑炎是自身免疫性脑炎最常见的形式,表现为各种精神症状,包括行为和认知障碍、运动障碍、意识减退、言语困难、癫痫发作和自主神经功能障碍。自主神经功能障碍可能包括体温过高、呼吸暂停、低血压、心动过速以及窦房结功能障碍(SND)的危及生命的表现,如心动过缓、窦性停搏或窦性静止以及心搏停止。SND 的严重程度和重要性至关重要,因为这些患者进展为心搏停止性心脏骤停并不罕见,这可能导致发病和死亡。因此,我们报告一例 18 岁患有抗 NMDAR 脑炎的女性病例,该患者经历了多次窦性停搏/静止和心搏停止性心脏骤停,所有情况下在成功进行心肺复苏后均恢复了自主循环,最终需要植入永久性起搏器。此外,我们进行了文献综述,并分析了 23 例有 SND 表现(包括窦性停搏/静止或心搏停止性心脏骤停)的类似抗 NMDAR 脑炎病例,以确定常见危险因素并描述管理策略和结果。此外,我们研究了畸胎瘤与 SND 中永久性起搏器使用之间的潜在关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e67/11318722/025bbe1b5f53/cureus-0016-00000064472-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e67/11318722/b5d517085439/cureus-0016-00000064472-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e67/11318722/025bbe1b5f53/cureus-0016-00000064472-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e67/11318722/b5d517085439/cureus-0016-00000064472-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e67/11318722/025bbe1b5f53/cureus-0016-00000064472-i02.jpg

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本文引用的文献

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Eur J Case Rep Intern Med. 2023 Jul 6;10(8):003974. doi: 10.12890/2023_003974. eCollection 2023.
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Clinical study of autonomic dysfunction in patients with autoimmune encephalitis.自身免疫性脑炎患者自主神经功能障碍的临床研究。
Immunobiology. 2023 Sep;228(5):152711. doi: 10.1016/j.imbio.2023.152711. Epub 2023 Jul 26.
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Bradycardia in a Woman Presenting with Altered Behaviour.一名行为改变女性的心动过缓
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Clinical Study of Autonomic Dysfunction in Patients With Anti-NMDA Receptor Encephalitis.抗N-甲基-D-天冬氨酸受体脑炎患者自主神经功能障碍的临床研究
Front Neurol. 2021 Feb 5;12:609750. doi: 10.3389/fneur.2021.609750. eCollection 2021.
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Anti-N-methyl-d-aspartate Receptor Encephalitis Related Sinus Node Dysfunction and the Lock-Step Phenomenon.抗N-甲基-D-天冬氨酸受体脑炎相关的窦房结功能障碍及同步现象
Am J Med Case Rep. 2020;8(12):503-507. doi: 10.12691/ajmcr-8-12-20. Epub 2020 Sep 25.
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An update on anti-NMDA receptor encephalitis for neurologists and psychiatrists: mechanisms and models.神经科医生和精神科医生对抗 NMDA 受体脑炎的最新认识:发病机制和模型。
Lancet Neurol. 2019 Nov;18(11):1045-1057. doi: 10.1016/S1474-4422(19)30244-3. Epub 2019 Jul 17.
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