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抗 N-甲基-D-天冬氨酸受体和α-烯醇化酶氨基端抗体双阳性患者的格斯特曼综合征

Gerstmann's Syndrome in a Patient Double-positive for Antibodies against the N-methyl-D-aspartate Receptor and NH-terminal of α-enolase.

机构信息

Department of Neurology, Graduate School of Medicine, Chiba University, Japan.

Department of Neurology, Eastern Chiba Medical Center, Japan.

出版信息

Intern Med. 2021 May 1;60(9):1463-1468. doi: 10.2169/internalmedicine.6344-20. Epub 2020 Nov 23.

DOI:10.2169/internalmedicine.6344-20
PMID:33229813
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8170245/
Abstract

We herein report a case of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis concurrent with NH-terminal of α-enolase (NAE) antibodies. A 36-year-old Japanese woman presented with Gerstmann's syndrome followed by jerky involuntary movements, seizure, autonomic instability, and consciousness disturbance. NAE antibodies were detected in the serum; however, NMDAR antibodies were identified in the cerebrospinal fluid with a cell-based assay, confirming the diagnosis of anti-NMDAR encephalitis. This case highlights the fact that Gerstmann's syndrome can be a manifestation of anti-NMDAR encephalitis and that NAE may be identified concurrently with NMDAR antibodies, suggesting that the diagnosis of Hashimoto encephalopathy requires the reasonable exclusion of alternative diagnoses, including anti-NMDAR encephalitis.

摘要

我们在此报告一例抗 N-甲基-D-天冬氨酸受体(NMDAR)脑炎合并 N-末端α-烯醇化酶(NAE)抗体阳性病例。一名 36 岁日本女性以格斯特曼综合征起病,随后出现不自主肌阵挛、癫痫、自主神经不稳定和意识障碍。血清中检测到 NAE 抗体;然而,通过细胞检测在脑脊液中发现了 NMDAR 抗体,从而确诊为抗 NMDAR 脑炎。本病例强调了格斯特曼综合征可能是抗 NMDAR 脑炎的一种表现形式,并且 NAE 可能与 NMDAR 抗体同时出现,提示桥本脑病的诊断需要合理排除其他诊断,包括抗 NMDAR 脑炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73d/8170245/0d699798aaf6/1349-7235-60-1463-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73d/8170245/f6fa20b8980f/1349-7235-60-1463-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73d/8170245/c654d987b700/1349-7235-60-1463-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73d/8170245/0d699798aaf6/1349-7235-60-1463-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73d/8170245/f6fa20b8980f/1349-7235-60-1463-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73d/8170245/c654d987b700/1349-7235-60-1463-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73d/8170245/0d699798aaf6/1349-7235-60-1463-g003.jpg

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本文引用的文献

1
Reader response: Hashimoto encephalopathy in the 21st century.读者回应:21世纪的桥本脑病
Neurology. 2020 Dec 8;95(23):1067-1068. doi: 10.1212/WNL.0000000000011100.
2
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.
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Hashimoto encephalopathy in the 21st century.21 世纪的桥本脑病。
Neurology. 2020 Jan 14;94(2):e217-e224. doi: 10.1212/WNL.0000000000008785. Epub 2019 Dec 27.
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Multiple co-existing antibodies in autoimmune encephalitis: A case and review of the literature.自身免疫性脑炎中存在多种共存抗体:病例报告及文献复习。
J Neuroimmunol. 2019 Dec 15;337:577084. doi: 10.1016/j.jneuroim.2019.577084. Epub 2019 Oct 15.
5
Serial brain MRI changes related to autoimmune pathophysiology in Hashimoto encephalopathy with anti-NAE antibodies: A case-series study.伴有抗NAE抗体的桥本脑病中与自身免疫病理生理学相关的系列脑MRI变化:一项病例系列研究
J Neurol Sci. 2019 Nov 15;406:116453. doi: 10.1016/j.jns.2019.116453. Epub 2019 Sep 7.
6
Persistent extreme delta brush in anti-NMDA-receptor encephalitis: Does it portend a poor prognosis?抗N-甲基-D-天冬氨酸受体脑炎中持续存在的极端δ波:它是否预示预后不良?
Epilepsy Behav Rep. 2019;12:100324. doi: 10.1016/j.ebr.2019.100324. Epub 2019 Jun 6.
7
Clinical variability of children with anti-N-methyl-D-aspartate receptor encephalitis in southern Brazil: a cases series and review of the literature.巴西南部抗 N-甲基-D-天冬氨酸受体脑炎患儿的临床变异性:病例系列及文献复习。
Neurol Sci. 2019 Feb;40(2):351-356. doi: 10.1007/s10072-018-3648-z. Epub 2018 Nov 20.
8
Anti-NMDA receptor encephalitis presenting as isolated aphasia in an adult.抗N-甲基-D-天冬氨酸受体脑炎在一名成人中表现为孤立性失语症。
Neurocase. 2018 Aug;24(4):188-194. doi: 10.1080/13554794.2018.1524915. Epub 2018 Oct 6.
9
Clinical presentation of anti-N-methyl-d-aspartate receptor and anti-voltage-gated potassium channel complex antibodies in children: A series of 24 cases.抗 N-甲基-D-天冬氨酸受体和电压门控钾通道复合物抗体在儿童中的临床特征:24 例系列病例。
Eur J Paediatr Neurol. 2018 Jan;22(1):135-142. doi: 10.1016/j.ejpn.2017.10.009. Epub 2017 Nov 7.
10
Clinical findings of a probable case of MM2-cortical-type sporadic Creutzfeldt-Jakob disease with antibodies to anti-N-terminus of α-enolase.一例可能为MM2-皮质型散发性克雅氏病且伴有抗α-烯醇化酶N端抗体病例的临床发现
Prion. 2017 Nov 2;11(6):454-464. doi: 10.1080/19336896.2017.1377876. Epub 2017 Oct 30.