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J Neurol Neurosurg Psychiatry. 2017 Jul;88(7):595-602. doi: 10.1136/jnnp-2016-315461. Epub 2017 Apr 24.
2
Associations of specific psychiatric disorders with isolated focal dystonia, and monogenic and idiopathic Parkinson's disease.特定精神障碍与孤立性局灶性肌张力障碍、单基因及特发性帕金森病的关联。
J Neurol. 2017 Jun;264(6):1076-1084. doi: 10.1007/s00415-017-8488-x. Epub 2017 Apr 11.
3
Unilateral predominance of abnormal movements: A characteristic feature of the pediatric anti-NMDA receptor encephalitis?异常运动的单侧优势:小儿抗N-甲基-D-天冬氨酸受体脑炎的一个特征性表现?
Epilepsy Behav Case Rep. 2017 Jan 18;7:42-44. doi: 10.1016/j.ebcr.2016.12.002. eCollection 2017.
4
Red Flags: Clinical Signs for Identifying Autoimmune Encephalitis in Psychiatric Patients.警示信号:识别精神科患者自身免疫性脑炎的临床体征
Front Psychiatry. 2017 Feb 16;8:25. doi: 10.3389/fpsyt.2017.00025. eCollection 2017.
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Ataxia in children: early recognition and clinical evaluation.儿童共济失调:早期识别与临床评估
Ital J Pediatr. 2017 Jan 13;43(1):6. doi: 10.1186/s13052-016-0325-9.
6
Autoimmune encephalitis in children: clinical phenomenology, therapeutics, and emerging challenges.儿童自身免疫性脑炎:临床现象学、治疗方法及新出现的挑战
Curr Opin Neurol. 2017 Jun;30(3):334-344. doi: 10.1097/WCO.0000000000000443.
7
High Incidence and Prevalence of Drug-Related Movement Disorders in Young Patients With Psychotic Disorders.精神病性障碍青年患者中药物相关运动障碍的高发病率和高患病率。
J Clin Psychopharmacol. 2017 Apr;37(2):231-238. doi: 10.1097/JCP.0000000000000666.
8
Autoimmune Encephalitides: A Broadening Field of Treatable Conditions.自身免疫性脑炎:一个不断拓展的可治疗疾病领域。
Neurologist. 2017 Jan;22(1):1-13. doi: 10.1097/NRL.0000000000000087.
9
Anti- N-Methyl-d-Aspartate (NMDA) Receptor Encephalitis.抗N-甲基-D-天冬氨酸(NMDA)受体脑炎
J Child Neurol. 2017 Feb;32(2):243-245. doi: 10.1177/0883073816675557. Epub 2016 Nov 22.
10
Gait Disturbance as the Presenting Symptom in Young Children With Anti-NMDA Receptor Encephalitis.步态障碍作为抗N-甲基-D-天冬氨酸受体脑炎幼儿的首发症状
Pediatrics. 2016 Sep;138(3). doi: 10.1542/peds.2016-0901. Epub 2016 Aug 16.

偏侧共济失调:青少年抗N-甲基-D-天冬氨酸受体抗体介导的脑炎的一种新表现形式。

Hemiataxia: A Novel Presentation of Anti-NMDA Receptor Antibody Mediated Encephalitis in an Adolescent.

作者信息

Phillips Greg D, Jones Gillian N, Callaghan Maureen, DiFazio Marc P

机构信息

Department of Neurology, Madigan Army Medical Center, Joint Base Madigan McChord, 9040 Jackson Ave, Tacoma, WA 98431, USA.

Department of Neurology, Children's National Health System, 111 Michigan Ave NW, Washington, DC 20010, USA.

出版信息

Case Rep Psychiatry. 2017;2017:1310465. doi: 10.1155/2017/1310465. Epub 2017 Dec 3.

DOI:10.1155/2017/1310465
PMID:29333310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5733199/
Abstract

Anti-NMDA receptor antibody associated encephalitis as a cause of new-onset neuropsychiatric manifestations in children and adults can represent a significant diagnostic challenge for clinicians. Clinical signs often include encephalopathy, new-onset psychosis, and movement phenomenon. Although orofacial dyskinesias were initially identified as a characteristic movement phenomenon in this type of encephalitis, an expanded range of abnormalities has recently been reported, including isolated ataxia. We report a case of isolated hemiataxia in a young adult with mild initial psychiatric manifestations. A personal and family history of preceding neuropsychiatric symptoms produced diagnostic confusion and resulted in a significant diagnostic and therapeutic delay. Our case confirms the unilateral movement manifestations that have been emphasized in recent reports. Additionally, it confirms the need for involvement of neurologic as well as psychiatric services in the evaluation of such cases and emphasizes the importance of the neurologic examination in presentations with an initial psychiatric predominance.

摘要

抗N-甲基-D-天冬氨酸受体抗体相关脑炎作为儿童和成人新发神经精神症状的一个病因,对临床医生而言可能是一项重大的诊断挑战。临床体征通常包括脑病、新发精神病和运动现象。尽管口面部运动障碍最初被认定为这类脑炎的一种特征性运动现象,但最近报告的异常范围有所扩大,包括孤立性共济失调。我们报告一例年轻成人发生孤立性偏侧共济失调,最初有轻度精神症状。既往神经精神症状的个人史和家族史造成诊断混淆,导致显著的诊断和治疗延误。我们的病例证实了近期报告中所强调的单侧运动表现。此外,它证实了在此类病例评估中需要神经科和精神科服务的参与,并强调了在以精神症状为主的初发表现中进行神经系统检查的重要性。