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Fever induced refractory epileptic encephalopathy in school age children

Fever induced refractory epileptic encephalopathy in school age children

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Fever induced refractory epileptic encephalopathy in school age children (FIRES) is a devastating condition which follows a prolonged refractory status epilepticus (SE) triggered by fever of unknown cause. The intractable perisylvian status epilepticus might persist for more than a month and results in severe cognitive impairment.

History

Several authors (Ismail & Kossoff, 2011; Lyon, Dodge, & Adams, 1961; Awaya,Hayashi,Osawa,Fukuyama, 1998; Mikaeloff et al., 2006; Kramer et al., 2005; Saito et al., 2007; Baxter et al., 2003)  have reported a presumed post encephalitic catastrophic epileptic encephalopathy resulting in refractory repetitive seizures associated with severe cognitive impairment. 

Mikaeloff et al in 2006 described this condition in a retrospective study of normally developing 14 children (mean age 7.5yrs) admitted with prolonged status epilepticus following a nonspecific febrile illness and called it Devastating Epileptic encephalopathy in School-age Children (DESC). 

The current term febrile infection-related epilepsy syndrome (FIRES) was proposed by Van Baalen et al in 2010 who published a retrospective multicenter case series of 22 previously healthy children aged 3-15yrs ( largest of the series) who developed prolonged and recurrent refractory seizures occurring 2-14 days (median 5 days) after fever onset.

Pathophysiology

Absence of either encephalitic changes in neuroimaging,marked CSF leukocytosis or inflammatory changes on biopsy suggests that the pathological process is not one of inflammation. The clinical course is charactarised by intractable recurrent/prolonged seizures suggesting neuronal hyperexcitation as the underlying cause.It is possible that the pathogenesis is immune mediated.

Clinical characteristics

  • The condition occurs in previously healthy normally developing children aged 3-15 years.
  • Characterised by an acute convulsive status epilepticus following a short febrile episode without any evidence of cns infection or inflammation. The status epilepticus is highly pharmacoresistant and can persist for more than a month
  • The seizures are characteristically bilateral perisylvian with propagation to the frontal lobes and are extremely frequent and refractory
  • The acute phase is followed by a chronic pharmacoresistant epilepsy associated with severe cognitive impairment mainly involving language, memory and behaviour. There is no latent period between the progression from acute to chronic phase.

Neurophysiology

 
EEG shows diffuse slowing or multifocal discharges
 

Neuroimaging

18-FDG PET FIRESPlain MRI is often normal, although selective bilateral hippocampal abnormalities including atrophy and hypersignal have been reported.18F-FDG PET studies (Mazzuca et al., 2011) have shown widepsread interictal hypometabolic network including the temporoparietal and orbitofrontal cortices bilaterally. The hypometabolic areas corresponded to the electroclinical seizures involving the temporofrontal cortex bilaterally as well as to the neuropsychologic findings.

 Neuropsychology

Neuropsychological deficits mainly involve language, frontal functions, behaviour and memory
 

Treatment

The condition is characteristically highly refractory to treatment. The efficacy of ketogenic diet as an alternative to pharmacotherapy in FIRES has been reported with favourable outcomes (Nabbout et al., 2010;Villeneuve et al., 2009) . A major contraindication to the ketogenic diet during status epilepticus is posisble pyruvate carboxylase and beta oxidation deficiencies. However these conditions are rare and easily diagnosed. There are no randomized controlled trials available on the use of the ketogenic diet in status epilepticus
 

References

  1. Ismail FY, Kossoff EH (November 2011). "AERRPS, DESC, NORSE, FIRES: multi-labeling or distinct epileptic entities?". Epilepsia 52 (11): e185–9. doi:10.1111/j.1528-1167.2011.03293.x. PMID22004046
  2. LYON G, DODGE PR, ADAMS RD (December 1961). "The acute encephalopathies of obscure origin in infants and children". Brain : a Journal of Neurology 84: 680–708. PMID14467623
  3. Awaya Y,Hayashi K,Osawa M,Fukuyama Y. A peculiar type of postencephalitis epilepty [abstract], Epilepsia. 1998; 39(suppl):S99
  4. Mikaeloff Y, Jambaqué I, Hertz-Pannier L, et al. (April 2006). "Devastating epileptic encephalopathy in school-aged children (DESC): a pseudo encephalitis". Epilepsy Res. 69 (1): 67–79 PMID16469483
  5. Baxter P, Clarke A, Cross H, et al. (September 2003). "Idiopathic catastrophic epileptic encephalopathy presenting with acute onset intractable status". Seizure : the Journal of the British Epilepsy Association 12 (6): 379–87 PMID12915084
  6. Kramer U, Shorer Z, Ben-Zeev B, Lerman-Sagie T, Goldberg-Stern H, Lahat E (March 2005). "Severe refractory status epilepticus owing to presumed encephalitis". Journal of Child Neurology 20 (3): 184–7 PMID15832606
  7. Saito Y, Maegaki Y, Okamoto R, Ogura K, Togawa M, Nanba Y, Inoue T, Takahashi Y, Ohno K (April 2007). "Acute encephalitis with refractory, repetitive partial seizures: case reports of this unusual post-encephalitic epilepsy". Brain & Development 29 (3): 147–56 PMID17008042
  8. van Baalen A, Häusler M, Boor R, Rohr A, Sperner J, Kurlemann G, Panzer A, Stephani U, Kluger G (July 2010). "Febrile infection-related epilepsy syndrome (FIRES): a nonencephalitic encephalopathy in childhood". Epilepsia 51 (7): 1323–8 PMID20345937
  9. Mazzuca M, Jambaque I, Hertz-Pannier L, Bouilleret V, Archambaud F, Caviness V, Rodrigo S, Dulac O, Chiron C (January 2011). "18F-FDG PET Reveals Frontotemporal Dysfunction in Children with Fever-Induced Refractory Epileptic Encephalopathy". Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine 52 (1): 40–7 PMID21149491
  10. Nabbout R, Mazzuca M, Hubert P, Peudennier S, Allaire C, Flurin V, Aberastury M, Silva W, Dulac O (October 2010). "Efficacy of ketogenic diet in severe refractory status epilepticus initiating fever induced refractory epileptic encephalopathy in school age children (FIRES)". Epilepsia 51 (10): 2033–7 PMID20813015
  11. Villeneuve N, Pinton F, Bahi-Buisson N, Dulac O, Chiron C, Nabbout R (April 2009). "The ketogenic diet improves recently worsened focal epilepsy". Developmental Medicine and Child Neurology 51 (4): 276–81 PMID19191829
 
http://icnapedia.org/wiki/epileptic-encephalopathies/2489
BH - Nothing to disclose.
  • July 16, 2012 (BH) article uploaded to live site
  • Feb 11, 2015 (BH) minor edit
APA Style
Fever induced refractory epileptic encephalopathy in school age children. (n.d.). In ICNApedia. Retrieved November 25,2017 09:08:48 from http://icnapedia.org/wiki/epileptic-encephalopathies/2489
MLA Style
"Fever induced refractory epileptic encephalopathy in school age children." ICNApedia: The Child Neurology Knowledge Environment, Inc. July 22, 2017. Web. November 25,2017 09:08:48
AMA Style
ICNApedia contributors. Fever induced refractory epileptic encephalopathy in school age children. ICNApedia, The Child Neurology Knowledge Environment. July 22, 2017. Available at: http://icnapedia.org/wiki/epileptic-encephalopathies/2489.Accessed November 25,2017 09:08:48.

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