Abstract

Investigators at Tel-Aviv Sourasky Medical Center, and three other medical centers in Israel, obtained data, prospectively, on all children presenting in the emergency departments from January 2008 to March 2010 with prolonged febrile seizures.

Highlights

  • Using modified adult guidelines (Zuliani L, et al J Neurol Neurosurg Psychiatry 2012 Jun;83(6):638-45), patients were classified as having definite autoimmune epilepsy in 5, probable in 1, possible in 3, unlikely in 2, and unknown in 2 patients, according to the neuronal surface or GAD antibodies, and response to immune therapy

  • Classical NMDAR encephalitis was diagnosed in 3 patients, VGKC in 2, limbic encephalitis with negative antibodies in 2, epilepsy with other autoimmune diseases in 3 (1 with GAD antibodies), fever-induced refractory epileptic encephalopathy in school-aged children (FIRES) in 2, and epileptic encephalopathy associated with VGKC antibodies in 1

  • Seven with suspected autoimmune epilepsy were positive for neuronal surface antibodies (NMDAR, VGKC-complex, and GAD)

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Summary

Introduction

Using modified adult guidelines (Zuliani L, et al J Neurol Neurosurg Psychiatry 2012 Jun;83(6):638-45), patients were classified as having definite autoimmune epilepsy in 5, probable in 1, possible in 3, unlikely in 2, and unknown in 2 patients, according to the neuronal surface or GAD antibodies, and response to immune therapy. Classical NMDAR encephalitis was diagnosed in 3 patients, VGKC in 2, limbic encephalitis with negative antibodies in 2, epilepsy with other autoimmune diseases in 3 (1 with GAD antibodies), fever-induced refractory epileptic encephalopathy in school-aged children (FIRES) in 2, and epileptic encephalopathy associated with VGKC antibodies in 1.

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