John Libbey Eurotext

Epileptic Disorders

The Educational Journal of the International League Against Epilepsy

Clinical-radiological-pathological correlation in an unusual case of refractory epilepsy: a two-year journey of whodunit! Volume 20, numéro 1, February 2018

Illustrations

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Tableaux

Auteurs
1 Department of Neurology, SCTIMST, Thiruvananthapuram, Kerala
2 Department of Imaging Studies and Interventional Radiology, SCTIMST, Trivandrum
3 Department of Neuropathology, NIMHANS, Bangalore, Karnataka
4 Amrita Institute of Medical Sciences, Edapally, Kochi, Kerala
5 Department of Neurology, JIPMER, Pondicherry
6 Department of Neurosurgery, SCTIMST, Thiruvananthapuram, Kerala
7 Department of Imaging Studies and Interventional Radiology, SCTIMST, Trivandrum, Kerala, India
* Correspondence: Ramshekhar N Menon Department of Neurology, SCTIMST, Thiruvananthapuram 695011, Kerala, India
  • Mots-clés : refractory focal epilepsy, peri-ictal oedema, N-methyl-D-aspartate receptor (NMDAR) antibody, focal encephalitis pathology
  • DOI : 10.1684/epd.2018.0955
  • Page(s) : 51-9
  • Année de parution : 2018

New-onset refractory focal epilepsy poses significant challenges to the clinician in the absence of specific diagnostic biomarkers. Differential diagnoses based on imaging may be expanded by a veritable spectrum of peri-ictal imaging findings that may mask the underlying substrate. We report a 13-year-old girl who presented with refractory focal seizures of left parieto-occipital origin with cytotoxic gyral oedema noted over the same region on imaging. Despite an initial negative autoantibody profile, the patient was treated with immunosuppression, followed by serial relapses requiring immune-modulation. Over the next year, her syndrome persisted as focal left posterior cortex epilepsy that necessitated occipital lobectomy, following a relapsing-remitting radiological profile, consistent with peri-ictal MRI changes. Histopathology was inconclusive for any definitive substrate. After a period of quiescence, she developed focal motor seizures of right hemispheric origin with progressive encephalopathy, at which point a repeat cerebrospinal fluid anti-N-methyl-D-aspartate receptor antibody profile returned positive. The patient was managed with steroids and rituximab with a good clinical outcome. We hypothesise that persistent or relapsing-remitting focal gyral oedema in unexplained refractory focal epilepsy mandates consideration of focal encephalitis secondary to autoimmunity, and late appearance of intrathecal auto-antibody synthesis correlates with evolution into a more diffuse disease.