The Treatment and Follow-Up of Anti-LGI1 Limbic Encephalitis

被引:12
作者
Yu, Jinbei [1 ,2 ]
Yu, Xuefan [1 ]
Fang, Shaokuan [1 ]
Zhang, Ying [1 ]
Li, Weihong [1 ,2 ]
机构
[1] Jilin Univ, Hosp 1, Dept Neurol, Changchun 130023, Peoples R China
[2] Prevent & Management Ctr Epilepsy, Changchun, Peoples R China
关键词
Antibodies; Follow-up; LGI1 limbic encephalitis; ANTIBODIES; SEIZURES; FORM;
D O I
10.1159/000441944
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: This study aims to retrospectively study clinical characteristics, diagnosis, treatment and follow-up visits in patients with anti-leucine-rich glioma inactivated-1 (LGI1) limbic encephalitis (LE) for prompting the early diagnosis and efficacious treatment of this disease. Methods: Four anti-LGI1 LE patients were hospitalized in the Department of Neurology at the First Hospital of Jilin University. Data from their clinical manifestations, diagnoses, treatments and follow-up visits were analyzed. Results: Four patients with anti-LGI1 LE were characterized by hypomnesia, mental and behavior disorder, faciobrachial dystonic seizures (FBDS), seizures accompanied by pathological changes in the limbic system, obstinate hyponatremia and positive detection of anti-LGI1 antibody. In this study, we found that 1 patient initially presented with an abnormal sensation and had a subsequent FBDS, inconsistent with normal cases of anti-LGI1 LE. This patient had abnormalities in the basal ganglia region identified with head MRI, unlike most cases, which report abnormalities in the limbic system by positron emission tomography/CT scan. Finally, 3 of our patients with FBDS were treated with antiepileptic drugs as well as immune modulatory treatment, and they responded well. Conclusions: We identified new characteristics in clinical manifestation, diagnosis and treatment of anti-LGI1 LE, which contribute to a better understanding of this disease and help improve its early diagnosis and efficacious treatment. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:5 / 11
页数:7
相关论文
共 18 条
  • [11] Outcome of limbic encephalitis with VGKC-complex antibodies: relation to antigenic specificity
    Malter, M. P.
    Frisch, C.
    Schoene-Bake, J. C.
    Helmstaedter, C.
    Wandinger, K. P.
    Stoecker, W.
    Urbach, H.
    Surges, R.
    Elger, C. E.
    Vincent, A. V.
    Bien, C. G.
    [J]. JOURNAL OF NEUROLOGY, 2014, 261 (09) : 1695 - 1705
  • [12] Antibodies to Glutamic Acid Decarboxylase Define a Form of Limbic Encephalitis
    Malter, Michael P.
    Helmstaedter, Christoph
    Urbach, Horst
    Vincent, Angela
    Bien, Christian G.
    [J]. ANNALS OF NEUROLOGY, 2010, 67 (04) : 470 - 478
  • [13] Park S, 2015, CLIN NUCL MED, V40, P156, DOI 10.1097/RLU.0000000000000546
  • [14] Limbic Encephalitis and Related Cortical Syndromes
    Rubio-Agusti, Ignacio
    Salavert, Miguel
    Bataller, Luis
    [J]. CURRENT TREATMENT OPTIONS IN NEUROLOGY, 2013, 15 (02) : 169 - 184
  • [15] Limbic encephalitis and variants:: Classification, diagnosis and treatment
    Tuzun, Erdem
    Dalmau, Josep
    [J]. NEUROLOGIST, 2007, 13 (05) : 261 - 271
  • [16] Potassium channel antibody-associated encephalopathy: a potentially immunotherapy-responsive form of limbic encephalitis
    Vincent, A
    Buckley, C
    Schott, JM
    Baker, I
    Dewar, BK
    Detert, N
    Clover, L
    Parkinson, A
    Bien, CG
    Omer, S
    Lang, B
    Rossor, MN
    Palace, J
    [J]. BRAIN, 2004, 127 : 701 - 712
  • [17] Autoantibodies associated with diseases of the CNS: new developments and future challenges
    Vincent, Angela
    Bien, Christian G.
    Irani, Sarosh R.
    Waters, Patrick
    [J]. LANCET NEUROLOGY, 2011, 10 (08) : 759 - 772
  • [18] Wieser S, 2005, EPILEPTIC DISORD, V7, P205