Refractory epilepsy secondary to anti-GAD encephalitis treated with DBS post SEEG evaluation: a novel case report based on stimulation findings

被引:11
|
作者
Gillinder, Lisa [1 ,2 ]
Lehn, Alexander [2 ,3 ]
Papacostas, Jason [1 ]
Olson, Sarah [2 ]
Blum, Stefan [2 ,3 ]
Dionisio, Sasha [1 ,2 ]
机构
[1] Mater Hosp, Mater Adv Epilepsy Unit, South Brisbane, Qld, Australia
[2] Princess Alexandra Hosp, Dept Neurol & Neurosurg, Woolloongabba, Qld, Australia
[3] Mater Hosp, Mater Ctr Neurosci, South Brisbane, Qld, Australia
关键词
anti-GAD antibody encephalitis; refractory epilepsy; deep brain stimulation; GLUTAMIC-ACID DECARBOXYLASE; TEMPORAL-LOBE EPILEPSY; ELECTRICAL-STIMULATION; INTRACTABLE EPILEPSY; LIMBIC ENCEPHALITIS; BRAIN-STIMULATION; ANTERIOR NUCLEUS; THALAMUS; ONSET;
D O I
10.1684/epd.2018.0993
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report a case of medically refractory anti-GAD encephalitis which was treated with deep brain stimulation (DBS) after seizure termination was achieved using cortical stimulation during stereo-electroencephalography (SEEG) evaluation. The patient underwent bilateral SEEG implantation and cortical stimulation. Upon stimulation, mimicking the intrinsic seizures (at 1Hz), it was possible to induce seizures with typical semiology, on multiple attempts. Stimulation during these seizures with high frequency (50Hz) resulted in complete termination of the seizure. DBS was inserted after the SEEG evaluation, targeting the bilateral anterior nucleus of the thalamus. There was a sustained reduction in seizure frequency and severity 12 months post insertion. There were also improvements in quality of life. To the best of our knowledge, this is the only case reported in which DBS was successfully used to treat refractory epilepsy in a patient with seizures that were proven to be responsive to electrical stimulation during SEEG recording.
引用
收藏
页码:451 / 456
页数:6
相关论文
共 5 条
  • [1] Autoimmune limbic encephalitis secondary to anti-GAD antibodies? A case report
    Boers, P
    Somerville, E
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2005, 238 : S116 - S116
  • [2] Super refractory status epilepticus secondary to anti-GAD antibody encephalitis successfully treated with aggressive immunotherapy
    Jaafar, Fatima
    Haddad, Laith
    Koleilat, Nadia
    Sharara-Chami, Rana
    Shbarou, Rolla
    EPILEPSY & BEHAVIOR REPORTS, 2020, 14
  • [3] Anti-GAD positive autoimmune encephalitis presenting with dementia, psychiatric symptoms and MS findings on the MRI: A case report
    Alencar, J. M. D.
    Ribeiro, T. A. G. J.
    Diniz, D. S.
    Melo, G. D. S.
    Bezerra, I. M. L.
    Oliveira Junior, R. M. D.
    Silva, D. J. D.
    Caixeta, L. F.
    Mendonca, H. R. S.
    Mendes, G. M.
    Silva Filho, H. F. D.
    Canedo, R. S. N. A.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2017, 381 : 536 - 536
  • [4] Successfully treated anti-GAD limbic encephalitis in a 15-year-old diabetic boy with intravenous immunoglobulin: case report
    Fattahzadeh Ardalani, Ghassem
    Khanghah, Ali Samady
    Jahanpanah, Mohammad
    Mokhtari, Diana
    Khanghah, Parisa Samady
    ANNALS OF MEDICINE AND SURGERY, 2024, 86 (02): : 1173 - 1181
  • [5] Novel FDG-PET Findings in Anti-NMDA Receptor Encephalitis: A Case Based Report
    Maqbool, Mohsin
    Oleske, Deanna A.
    Huq, A. H. M.
    Salman, Bassel A.
    Khodabakhsh, Kevin
    Chugani, Harry T.
    JOURNAL OF CHILD NEUROLOGY, 2011, 26 (10) : 1325 - 1328