Photosensitive Temporal Lobe Epilepsy: a Case Report
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A Small Number of People Have What Is Known As Reflex Epilepsy, In
A small number of people have what is known What are the features of reflex epilepsy? as reflex epilepsy, in which seizures are set off There are many different types of reflex by specific stimuli. These can include flashing epilepsy, depending on the area of the brain that lights, a flickering computer “monitor”, sudden is affected. Seizure stimuli may be very specific, noises, a particular piece of music, or the phone or they may be broad categories. They can ringing. Some people even have seizures when include: they think about a particular subject or see their own hand! flashing or flickering lights, including computer monitors or video games. This is What are other terms for reflex epilepsy? called photosensitive epilepsy. It is the most Other terms for reflex epilepsy that you may common childhood form of reflex epilepsy, come across include: and the child may eventually outgrow it. the sight of a particular pattern; this is called epilepsy with reflex seizures visual pattern reflex epilepsy sensory precipitation epilepsy thinking about certain things stimulus sensitive epilepsy performing a certain task, such as typing; this is called praxis-induced epilepsy There are also many terms for specific types of reading reflex epilepsy. language-related stimuli such as writing, listening to speech, singing, or reciting What causes reflex epilepsy? certain passages of music; this is called The seizure stimulus is not the underlying cause musicogenic epilepsy of the epilepsy. Rather, it sends a particular certain sounds; this is called audiogenic message to a sensitive, seizure-prone area of the epilepsy brain, excites the neurons there, and causes a surprises or startles seizure. -
Photosensitive Epilepsy
photosensitive epilepsy factsheet If you have epilepsy you may be able to identify triggers – situations that set off your seizures. Common triggers include stress or tiredness. If seizures are triggered by flashing lights 1 or certain patterns, this is called photosensitive epilepsy. how common is photosensitive epilepsy? how is photosensitive epilepsy treated? Around 1 in 100 people has epilepsy, and of these Photosensitive epilepsy usually responds well to people, around 3% have photosensitive epilepsy. anti-epileptic drugs (AEDs) that treat generalised Photosensitive epilepsy is more common in children seizures (seizures that affect both sides of the brain and young people (up to 5%) and is less commonly at once). diagnosed after the age of 20. See our booklet and chart medication for epilepsy for more information. how can I tell if I am photosensitive? Many people know this if they have a seizure Triggers are individual, but the following sources when they are exposed to flashing lights or patterns in themselves are not generally likely to trigger as a photosensitive trigger will usually cause photosensitive seizures. See over the page for a seizure straightaway. possible triggers and what increases the risk. An electroencephalogram (EEG) may include testing • UK TV programme content. Ofcom regulates for photosensitive epilepsy. This involves looking at a material shown on TV in the UK. The regulations light which will flash at different speeds. If this causes restrict the flash rate to three hertz or less, and any changes in brain activity the technician can stop they also restrict the area of screen allowed for the flashing light before a seizure develops. -
Seizure, New Onset
CLINICAL PATHWAY NEW ONSET SEIZURE Inclusion Criteria ALGORITHM 1. CONCERN FOR POSSIBLE SEIZURE • Age 6 months to 21 years • First-time seizure Exclusion Criteria • Status epilepticus (refer to status epilepticus pathway) Concern Unsure for possible Yes seizure? Obtain history and screening Obtain history and screening neurologic exam neurologic exam Consider differential diagnoses: Evaluate for possible provoking factors: • Breath holding • Fever/illness • Stereotypies/tics • Acute traumatic brain injury (TBI) ! • Vasovagal/syncope/vertigo • Central nervous system (CNS) infection Urgent call • Reflux • Tumor to ‘OneCall’ for: • Electrolyte imbalance • Ingestion • Suspected infantile spasm • Non epileptic seizure • Intoxication • Medically complex children • Electrolyte imbalance Off pathway: Consider outpatient referral to Neurology Off pathway: Provoked? Yes Address provoking factors No Continue to new onset unprovoked seizure algorithm on p.2 NEED REAL TIME HELP? CALL US! Call ‘OneCall’ at 720-777-3999 or 719-305-3999 (Colorado Springs) Page 1 of 17 CLINICAL PATHWAY ALGORITHM 2. NEW ONSET UNPROVOKED SEIZURE Inclusion Criteria • Age 6 months to 21 years New onset unprovoked • First-time unprovoked seizure seizure • Newly recognized seizure or epilepsy syndrome Exclusion Criteria • Provoked seizure: any seizure as a symptom of fever/illness, acute traumatic brain injury (TBI), Has central nervous system (CNS) infection, tumor, patient returned ingestion, intoxication, or electrolyte imbalance Consult inpatient • to baseline within No -
Valproate in Adolescents with Photosensitive Epilepsy with Generalized Tonic-Clonic Seizures Only
european journal of paediatric neurology 18 (2014) 13e18 Official Journal of the European Paediatric Neurology Society Original article Valproate in adolescents with photosensitive epilepsy with generalized toniceclonic seizures only Alberto Verrotti a,g, Salvatore Grosso b, Claudia D’Egidio a, Pasquale Parisi c, Alberto Spalice d, Piero Pavone e, Giuseppe Capovilla f, Sergio Agostinelli a,* a Department of Pediatrics, University of Chieti, Via dei Vestini 5, 66100 Chieti, Italy b Department of Pediatrics, University of Siena, Siena, Italy c Chair of Pediatrics, II Faculty of Medicine, “La Sapienza” University of Rome, Rome, Italy d Department of Pediatrics, I Faculty of Medicine, “La Sapienza” University of Rome, Rome, Italy e Division of Pediatric Neurology, University of Catania, Catania, Italy f Epilepsy Center, Department of Child Neuropsychiatry, C. Poma Hospital, Mantova, Italy g Department of Pediatrics, University of Perugia, Perugia, Italy article info abstract Article history: Aim: To assess the effects of valproate (VPA) on seizure response/control and photo- Received 17 December 2012 sensitivity (PS) in adolescents suffering from photosensitive epilepsy with generalized Received in revised form toniceclonic seizures only (EGTCS). 8 April 2013 Methods: We prospectively evaluated 55 adolescents with newly diagnosed EGTCS and PS at Accepted 29 June 2013 presentation, who received VPA monotherapy. Two phases of the study were defined and analysed separately. In the phase I, the electroclinical data of patients were compared over Keywords: three time points: T1 (at 6 months of treatment); T2 (at 12 months of treatment); and T3 (at Adolescents 36 months of treatment). In the phase II, only patients who stopped VPA were evaluated Valproate over a period of 12 months. -
The Relationship Between the Components of Idiopathic Focal Epilepsy
Journal of Pediatrics and Neonatal Care Review Article Open Access The relationship between the components of idiopathic focal epilepsy Abstract Volume 8 Issue 3 - 2018 The classification of epileptic syndromes in children is not a simple duty, it requires Cesar Ramon Romero Leguizamon a great clinical ability as well as some degree of experience. Until today there is no Department of Drug Design and Pharmacology, University of international consensus regarding the different diseases that are part of the Idiopathic Copenhagen, Denmark Focal Epilepsies However, these diseases are the most prevalent in children suffering from some type of epilepsy, for this reason it is important to know more about these, Correspondence: Cesar Ramon Romero Leguizamon their clinical characteristics, pathological findings in studies such as encephalogram, M.D., Department of Drug Design and Pharmacology Faculty resonance, polysomnography and others. In the same way, to explore the possible of Health and Medical Science, University of Copenhagen, genetic origins of many of these pathologies, that have been little explored and Denmark, Jagtev 160, 2100 Copenhagen, Denmark, become an important therapeutic goal. A description of the most relevant aspects of Email [email protected] atypical benign partial epilepsy, Landau-Kleffner syndrome, benign epilepsy with centrotemporal spikes, electrical status epilepticus during sleep and Panayiotopoulos Received: February 17, 2018 | Published: May 14, 2018 syndrome is presented in this review, Allowing physicians and family members of children suffering from these diseases to have a better understanding and establish in this way a better diagnosis and treatment in patients, as well as promote in the scientific community the interest to investigate more about these relevant pathologies in childhood. -
ILAE Classification and Definition of Epilepsy Syndromes with Onset in Childhood: Position Paper by the ILAE Task Force on Nosology and Definitions
ILAE Classification and Definition of Epilepsy Syndromes with Onset in Childhood: Position Paper by the ILAE Task Force on Nosology and Definitions N Specchio1, EC Wirrell2*, IE Scheffer3, R Nabbout4, K Riney5, P Samia6, SM Zuberi7, JM Wilmshurst8, E Yozawitz9, R Pressler10, E Hirsch11, S Wiebe12, JH Cross13, P Tinuper14, S Auvin15 1. Rare and Complex Epilepsy Unit, Department of Neuroscience, Bambino Gesu’ Children’s Hospital, IRCCS, Member of European Reference Network EpiCARE, Rome, Italy 2. Divisions of Child and Adolescent Neurology and Epilepsy, Department of Neurology, Mayo Clinic, Rochester MN, USA. 3. University of Melbourne, Austin Health and Royal Children’s Hospital, Florey Institute, Murdoch Children’s Research Institute, Melbourne, Australia. 4. Reference Centre for Rare Epilepsies, Department of Pediatric Neurology, Necker–Enfants Malades Hospital, APHP, Member of European Reference Network EpiCARE, Institut Imagine, INSERM, UMR 1163, Université de Paris, Paris, France. 5. Neurosciences Unit, Queensland Children's Hospital, South Brisbane, Queensland, Australia. Faculty of Medicine, University of Queensland, Queensland, Australia. 6. Department of Paediatrics and Child Health, Aga Khan University, East Africa. 7. Paediatric Neurosciences Research Group, Royal Hospital for Children & Institute of Health & Wellbeing, University of Glasgow, Member of European Refence Network EpiCARE, Glasgow, UK. 8. Department of Paediatric Neurology, Red Cross War Memorial Children’s Hospital, Neuroscience Institute, University of Cape Town, South Africa. 9. Isabelle Rapin Division of Child Neurology of the Saul R Korey Department of Neurology, Montefiore Medical Center, Bronx, NY USA. 10. Programme of Developmental Neurosciences, UCL NIHR BRC Great Ormond Street Institute of Child Health, Department of Clinical Neurophysiology, Great Ormond Street Hospital for Children, London, UK 11. -
A Prospective Open-Labeled Trial with Levetiracetam in Pediatric Epilepsy Syndromes: Continuous Spikes and Waves During Sleep Is Definitely a Target
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Seizure 20 (2011) 320–325 Contents lists available at ScienceDirect Seizure journal homepage: www.elsevier.com/locate/yseiz A prospective open-labeled trial with levetiracetam in pediatric epilepsy syndromes: Continuous spikes and waves during sleep is definitely a target S. Chhun a,b,c, P. Troude d, N. Villeneuve e, C. Soufflet a,b,f, S. Napuri g, J. Motte h, F. Pouplard i, C. Alberti d, S. Helfen j, G. Pons a,b,c, O. Dulac a,b,k, C. Chiron a,b,k,* a Inserm, U663, Paris, France b University Paris Descartes, Faculty of Medicine, Paris, France c APHP, Pediatric Clinical Pharmacology, Cochin-Saint Vincent de Paul Hospital, Paris, France d APHP, Unit of Clinical Research, Robert Debre Hospital, Paris, France e APHM, Neuropediatric Department, Marseille, France f APHP, Necker Hospital, Department of Functional Explorations, Paris, France g Neuropediatric Department, Rennes Hospital, France h Neuropediatric Department, American Memorial Hospital, Reims, France i Neuropediatric Department, Angers Hospital, France j APHP, Necker Hospital, Unit of Clinical Research, Paris, France k APHP, Necker Hospital, Neuropediatric Department, Paris, France ARTICLE INFO ABSTRACT Article history: Although LVT is currently extensively prescribed in childhood epilepsy, its effect on the panel of Received 12 October 2010 refractory epilepsy syndromes has not been entirely evaluated prospectively. In order to study the Received in revised form 17 December 2010 efficacy and safety of LVT as adjunctive therapy according to syndromes, we included 102 patients with Accepted 27 December 2010 refractory seizures (6 months to 15 years) in a prospective open-labeled trial. -
Prospective Evaluation of Interrater Agreement Between EEG Technologists and Neurophysiologists Isabelle Beuchat 1,2, Senubia Alloussi1,2, Philipp S
www.nature.com/scientificreports OPEN Prospective evaluation of interrater agreement between EEG technologists and neurophysiologists Isabelle Beuchat 1,2, Senubia Alloussi1,2, Philipp S. Reif1,2,3, Nora Sterlepper1,2, Felix Rosenow1,2 & Adam Strzelczyk 1,2* We aim to prospectively investigate, in a large and heterogeneous population, the electroencephalogram (EEG)-reading performances of EEG technologists. A total of 8 EEG technologists and 5 certifed neurophysiologists independently analyzed 20-min EEG recordings. Interrater agreement (IRA) for predefned EEG pattern identifcation between EEG technologists and neurophysiologits was assessed using percentage of agreement (PA) and Gwet-AC1. Among 1528 EEG recordings, the PA [95% confdence interval] and interrater agreement (IRA, AC1) values were as follows: status epilepticus (SE) and seizures, 97% [96–98%], AC1 kappa = 0.97; interictal epileptiform discharges, 78% [76–80%], AC1 = 0.63; and conclusion dichotomized as “normal” versus “pathological”, 83.6% [82–86%], AC1 = 0.71. EEG technologists identifed SE and seizures with 99% [98–99%] negative predictive value, whereas the positive predictive values (PPVs) were 48% [34– 62%] and 35% [20–53%], respectively. The PPV for normal EEGs was 72% [68–76%]. SE and seizure detection were impaired in poorly cooperating patients (SE and seizures; p < 0.001), intubated and older patients (SE; p < 0.001), and confrmed epilepsy patients (seizures; p = 0.004). EEG technologists identifed ictal features with few false negatives but high false positives, and identifed normal EEGs with good PPV. The absence of ictal features reported by EEG technologists can be reassuring; however, EEG traces should be reviewed by neurophysiologists before taking action. -
Panayiotopoulos Syndrome: a Debate
Letter to the Editor Epileptic Disord 2010; 12 (1): 91-4 Panayiotopoulos syndrome: a debate To the editor superbly illustrated by the syndrome of benign partial Yalcin et al. (2009) describe three patients with neuro- epilepsy with centro-temporal spikes, a syndrome that radiological abnormalities identifi ed on magnetic has robustly defi ed eponymous adoption for many resonance imaging (MRI), which they consider to be decades. “coincidental” and un-related to an underlying electro- clinical diagnosis of Panayiotopoulos syndrome Richard E. Appleton, Brian Tedman, (PS). While they propose that the MRI abnormalities Teresa Preston, Tam Foy demonstrated are coincidental and do not preclude The Roald Dahl EEG Department, the diagnosis of PS, there may be another explana- Paediatric Neurosciences Foundation Trust, tion. It could reasonably be argued that the radiolog- Alder Hey Children’s NHS Foundation Trust, ical abnormalities seen in their patients (particularly Liverpool L12 2AP, UK patients 2 and 3) are not coincidental and that these <[email protected]> patients have a symptomatic focal or multifocal epilepsy and not Panayiotopoulos syndrome. Response to the letter of R. Appleton, et al. Although an “expert consensus” has attempted to To the editor defi ne and classify the existence of PS (Ferrie et al., 2006), it does not necessarily follow that their opinion We welcome the comments of Appleton and his is correct. There appear to be ever-increasing reports colleagues regarding issues raised for a better under- of “atypical” cases of PS. On scientifi c grounds this standing of Panayiotopoulos syndrome (PS). must surely raise the question as to whether this does The authors argue that the 3 children we described represent a true “syndrome” as defi ned in both the had symptomatic focal or multifocal epilepsy not PS. -
Types of Photic-Induced Seizures and Epileptic Types Associated With
SEIZURE DISORDERS EPILEPTIC SYNDROMES AND PHOTOSENSITIVE SEIZURES The clinical features of different types of photic-induced seizures and epileptic syndromes characterized by visual sensitivity are reviewed from the University of Pisa, Italy, and Centre St Paul, Marseille, France. Seizure types associated with clinical photosensitivity include eyelid myoclonus, generalized myoclonic jerks, tonic-versive seizures, absence, generalized tonic clonic, and focal seizures. Epileptic syndromes with photic-induced seizures include benign myoclonic epilepsy in infancy, absence epilepsy, juvenile myoclonic epilepsy, epilepsy with myoclonic-astatic seizures, primary reading epilepsy, severe myoclonic epilepsy of infancy, photosensitive occipital lobe epilepsy, and progressive myoclonus epilepsies (PME). PME with photic sensitivity are symptoms of neuronal ceroid lipofuscinosis, Lafora's disease, Unverricht-Lundborg disease, and myoclonus epilepsy and ragged red fibers (MERRF). Visually induced seizures can be generalized or focal, idiopathic or symptomatic, or represent a pure reflex photosensitive epilepsy. (Guerrini R, Genton P. Epileptic syndromes and visually induced seizures. Epilepsia January 2004;45 (Suppl 1): 14- 18). (Reprints: Dr R Guerrini, Division of Child Neurology and Psychiatry, University of Pisa & IRCCS Fondazione Stella Maris, via dei Giacinti 2, 56018 Calambrone, Pisa, Italy). COMMENT. The treatment of photosensitive epilepsies involves preventive measures and antiepileptic medications (AED). (Covanis A et al. Epilepsia Jan 2004;45(Suppl l):40-45; Bureau M et al. Epilepsia Jan 2004;45(Suppl l):24-26). Preventive measures include the following: avoid stimuli (eg TV, videogames); use small TV, 100-Hz screen, remote control, sit >2 m away from screen, wear spectacles, avoid stress and fatigue. Usually a combination of avoidance of stimuli and an AED is necessary. -
Relation of Photosensitivity to Epileptic Syndromes
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.49.12.1386 on 1 December 1986. Downloaded from Journal of Neurology, Neurosurgery, and Psychiatry 1986;49:1386-1391 Relation of photosensitivity to epileptic syndromes P WOLF,* R GOOSSES Abteilungfiir Neurologie, Klinikum Charlottenburg der Freien Universitdt, Berlin, Federal Republic ofGermany SUMMARY Photosensitivity is the most common mode of seizure precipitation. It is age-related, more frequent in females, and most often found in generalised epilepsies. Little is known about its relation to individual epileptic syndromes. This study on 1062 epileptic patients who had 4007 split screen video EEG investigations revealed that the relation to generalised epilepsy is even more close than generally believed. Versive seizures with visual hallucinations was the only focal seizure type related to photosensitivity. Of the syndromes of generalised epilepsy, only childhood absence epi- lepsy, juvenile myoclonic epilepsy, and epilepsy with grand mal on awakening were related to photosensitivity. The closest correlation was with juvenile myoclonic epilepsy. This is confirmed by a relation to the poly-spike wave pattern, and by an increase of myoclonic seizures by intermittent light stimuli. No relation was found with early childhood syndromes of generalised epilepsy, or generalised tonic-clonic seizures in the evening, or, most remarkably, with juvenile absence epilepsy. guest. Protected by copyright. In generalised epilepsies with onset around puberty, photosensitivity could thus act as a patho- plastic factor. The female preponderance in both childhood absences and photosensitivity could be due to the same unknown factor. Photosensitivity does not necessarily signify epi- of increasing and decreasing frequency from 3 to 30 Hz were lepsy.' In connection with epilepsy, photosensitivity applied. -
Fostering Epilepsy Care in Europe All Rights Reserved
EPILEPSY IN THE WHO EUROPEAN REGION: Fostering Epilepsy Care in Europe All rights reserved. No part of this publication may be reproduced, stored in a database or retrieval system, or published, in any form or any way, electronically, mechanically, by print, photoprint, microfilm or any other means without prior written permission from the publisher. Address requests about publications of the ILAE/IBE/WHO Global Campaign Against Epilepsy: Global Campaign Secretariat SEIN P.O. Box 540 2130 AM Hoofddorp The Netherlands e-mail: [email protected] ISBN NR. 978-90-810076-3-4 Layout/ Printing: Paswerk Bedrijven, Cruquius, Netherlands Table of contents Foreword ................................................................................................................................................. 4 Preface ................................................................................................................................................. 5 Acknowledgements ........................................................................................................................................ 6 Tribute ................................................................................................................................................. 7 Abbreviations ................................................................................................................................................. 8 Background information on the European Region .........................................................................................