Autoimmune encephalitis accompanied with status epilepticus, dyskinesia and hypoventilation syndrome: A case report and literature review

WANG Qinying, GU Qin, YU Min, JIANG Dudu, ZHAN Qing

Journal of Neurology and Neurorehabilitation ›› 2017, Vol. 13 ›› Issue (2) : 98-103.

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Journal of Neurology and Neurorehabilitation ›› 2017, Vol. 13 ›› Issue (2) : 98-103. DOI: 10.12022/jnnr.2017-0021
Case Report

Autoimmune encephalitis accompanied with status epilepticus, dyskinesia and hypoventilation syndrome: A case report and literature review

  • WANG Qinying1, 2, GU Qin1, 2, YU Min1, 2, JIANG Dudu1, 2, ZHAN Qing1, 2
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Abstract

Objective: To summarize the clinical features of autoimmune encephalitis so as to reduce the clinical misdiagnosis. Methods: The diagnosis and treatment and the follow-up data of a young female patient with autoimmune encephalitis were reviewed retrospectively. Results: The patient had a fever as the initial symtom and the disease progressed rapidly with status epilepsy, motor disorders and hypoventilation syndrome. Immunotherapy was administered when the diagnosis of autoimmune encephalitis was confirmed. At the third month since the onset of the disease, the condition of the patient was gradually improved; at the fifteenth month, the patient achieved good prognosis. Conclusion: In clinical practice, a young patient with mental disorders, dyskinesia and epilepsy suspected of autoimmune encephalitis should receive detection of serum antibodies associated with autoimmune encephalitis and the cerebrospinal fluid test to make a definite diagnosis.

Key words

Encephalitis / Autoimmune encephalitis / Status epilepticus / Motor disorders

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WANG Qinying, GU Qin, YU Min, JIANG Dudu, ZHAN Qing. Autoimmune encephalitis accompanied with status epilepticus, dyskinesia and hypoventilation syndrome: A case report and literature review[J]. Journal of Neurology and Neurorehabilitation. 2017, 13(2): 98-103 https://doi.org/10.12022/jnnr.2017-0021

References

[1] Granerod J, Ambrose HE, Davies NW, et al. Causes of encephalitis and differences in their clinical presentations in England: a multicentre, population-based prospective study[J]. Lancet Infect Dis, 2010, 10(12):835-844.
[2] Irani SR, Gelfand JM, Al-Diwani A, et al. Cell-surface central nervous system autoantibodies: clinical relevance and emerging paradigms[J]. Ann Neurol, 2014, 76(2):168-184.
[3] Lopinto-Khoury C, Sperling MR. Autoimmune status epilepticus[J]. Curr Treat Options Neurol, 2013, 15(5):545-556.
[4] Gable MS, Sheriff H, Dalmau J, et al. The frequency of autoimmune N-methyl-D-aspartate receptor encephalitis surpasses that of individual viral etiologies in young individuals enrolled in the California Encephalitis Project[J]. Clin Infect Dis, 2012, 54(7):899-904.
[5] 矫黎东, 王向波. 自身免疫性脑炎临床研究进展[J]. 疑难病杂志, 2012, 13(12):1312-1314.
[6] 陆 卉, 张雅静. 自身免疫性脑炎临床鉴别诊断及治疗研究[J]. 中华医院感染学杂志, 2014, 24(6):1423-1425.
[7] Irani SR, Stagg CJ, Schott JM, et al. Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotype[J]. Brain, 2013, 136(Pt 10):3151-3162.
[8] Dalmau J, Gleichman AJ, Hughes EG, et al. Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies[J]. Lancet Neurol, 2008, 7(12):1091-1098.
[9] Irani SR, Michell AW, Lang B, et al. Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis[J]. Ann Neurol, 2011, 69(5):892-900.
[10] Dericioglu N, Vural A, Acar P, et al. Antiepileptic treatment for anti-NMDA receptor encephalitis: the need for video-EEG monitoring[J]. Epileptic Disord, 2013, 15(2):166-170.
[11] Nolan B, Plenk K, Carr D. Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis presenting to the emergency department with status epilepticus[J]. CJEM, 2014, 16(5):425-428.
[12] Finné Lenoir X, Sindic C, van Pesch V, et al. Anti-N-methyl-D-aspartate receptor encephalitis with favorable outcome despite prolonged status epilepticus[J]. Neurocrit Care, 2013, 18(1):89-92.
[13] Holzer FJ, Rossetti AO, Heritier-Barras AC, et al. Antibody-mediated status epilepticus: a retrospective multicenter survey[J]. Eur Neurol, 2012, 68(5):310-317.
[14] Gable MS, Gavali S, Radner A, et al. Anti-NMDA receptor encephalitis: report of ten cases and comparison with viral encephalitis[J]. Eur J Clin Microbiol Infect Dis, 2009, 28(12):1421-1429.
[15] Schmitt SE, Pargeon K, Frechette ES, et al. Extreme delta brush: a unique EEG pattern in adults with anti-NMDA receptor encephalitis[J]. Neurology, 2012, 79(11):1094?1100.
[16] Kayser MS, Kohler CG, Dalmau J. Psychiatric manifestations of paraneoplastic disorders[J]. Am J Psychiatry, 2010, 167(9):1039-1050.
[17] Bien CG, Vincent A, Barnett MH, et al. Immunopathology of autoantibody-associated encephalitides: clues for pathogenesis[J]. Brain, 2012, 135(Pt 5):1622-1638.
[18] 陈向军, 邓 波. 自身免疫性脑炎的诊断标准及其临床指导意义[J]. 中国临床神经科学, 2016, 24(3):336-340.

Funding

Youth Fund Project of Science and Technology Commission of Shanghai Municipality (No. 20164Y0073); Academic Research Project of Shanghai University of Traditional Chinese Medicine (No. 2016YG36); Course Construction Project of Shanghai University of Traditional Chinese Medicine (No. SHUTCMKCJSY2016090); Talents Training Program of Seventh People’s Hospital Affiliated to Shanghai University of Traditional Chinese Medicine (No. MZY2017-01)
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