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Epilepsy surgery in drug resistant temporal lobe epilepsy associated with neuronal antibodies

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F17%3A10373909" target="_blank" >RIV/00216208:11130/17:10373909 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064203:_____/17:10373909

  • Result on the web

    <a href="https://doi.org/10.1016/j.eplepsyres.2016.12.010" target="_blank" >https://doi.org/10.1016/j.eplepsyres.2016.12.010</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.eplepsyres.2016.12.010" target="_blank" >10.1016/j.eplepsyres.2016.12.010</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Epilepsy surgery in drug resistant temporal lobe epilepsy associated with neuronal antibodies

  • Original language description

    We assessed the outcome of patients with drug resistant epilepsy and neuronal antibodies who underwent epilepsy surgery. Retrospective study, information collected with a questionnaire sent to epilepsy surgery centers. Thirteen patients identified, with antibodies to GAD (8), Ma2 (2), Hu (1), LGI1 (1) or CASPR2 (1). Mean age at seizure onset: 23 years. Five patients had an encephalitic phase. Three had testicular tumors and five had autoimmune diseases. All had drug resistant temporal lobe epilepsy (median: 20 seizures/month). MRI showed unilateral temporal lobe abnormalities (mainly hippocampal sclerosis) in 9 patients, bilateral abnormalities in 3, and was normal in 1. Surgical procedures included anteromesial temporal lobectomy (10 patients), selective amygdalohippocampectomy (1), temporal pole resection (1) and radiofrequency ablation of mesial structures (1). Perivascular lymphocytic infiltrates were seen in 7/12 patients. One year outcome available in all patients, at 3 years in 9. At last visit 5/13 patients (38.5%) (with Ma2, Hu, LGI1, and 2 GAD antibodies) were in Engel&apos;s classes I or II. Epilepsy surgery may be an option for patients with drug resistant seizures associated with neuronal antibodies. Outcome seems to be worse than that expected in other etiologies, even in the presence of unilateral HS. Intracranial EEG may be required in some patients.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30103 - Neurosciences (including psychophysiology)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Epilepsy Research

  • ISSN

    0920-1211

  • e-ISSN

  • Volume of the periodical

    129

  • Issue of the periodical within the volume

    Januar

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    5

  • Pages from-to

    101-105

  • UT code for WoS article

    000394634300017

  • EID of the result in the Scopus database

    2-s2.0-85007490292