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Different presurgical characteristics and seizure outcomes in children with focal cortical dysplasia type I or II
Pavel Krsek, Tom Pieper, Anja Karlmeier, Michelle Hildebrandt, Dieter Kolodziejczyk, Peter Winkler, Elisabeth Pauli, Ingmar Blümcke and Hans Holthausen
Jazyk angličtina Země Spojené státy americké
Grantová podpora
NR8843
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Free Medical Journals
od 1997 do Před 1 rokem
Wiley Online Library (archiv)
od 1997-01-01 do 2012-12-31
Wiley Free Content
od 1997 do Před 4 lety
- MeSH
- atrofie patologie MeSH
- dítě MeSH
- elektroencefalografie MeSH
- financování organizované MeSH
- fluorodeoxyglukosa F18 diagnostické užití MeSH
- gliový fibrilární kyselý protein metabolismus MeSH
- hipokampus patologie MeSH
- imunohistochemie MeSH
- lidé MeSH
- magnetická rezonanční tomografie MeSH
- malformace mozkové kůry epidemiologie metabolismus patologie MeSH
- monoklonální protilátky metabolismus MeSH
- pooperační péče MeSH
- předoperační péče MeSH
- radiofarmaka diagnostické užití MeSH
- retrospektivní studie MeSH
- věk při počátku nemoci MeSH
- výsledek terapie MeSH
- záchvaty epidemiologie MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
PURPOSE: Cortical dysplasia (FCD) is a frequent cause of epilepsy in childhood. Two major pathological variants are distinguished, FCD type I and II. The aim of the study was to characterize differences between FCD type I and II with respect to imaging and EEG findings, clinical and neuropsychological presentations, and surgical outcome. METHODS: Forty children with refractory epilepsy and histopathologically confirmed FCD were retrospectively analyzed. FCD type I was identified in 24 and FCD type II in 16 patients. RESULTS: Characteristic MRI abnormalities in FCD type I included subtle white matter signal changes and regional reduction of the white matter volume. Typical MRI findings in FCD type II were increased cortical thickness, transmantle sign, gray-white matter junction blurring, fluid-attenuated inversion recovery (FLAIR) and proton density (PD) gray matter signal changes as well as T1w, and PD white matter signal changes. Continuous EEG slowing was significantly more common in patients with FCD type I. Children with FCD type I presented with lower levels of intelligence and were suffering more often from maladaptive behavior and behavioral disorders. Surgical outcome was significantly worse in the FCD type I group (seizure freedom was achieved in 21% FCD type I patients and in 75% FCD type II subjects, p < 0.001). CONCLUSIONS: Clinically important differences were found in children with distinct histopathological subtypes of FCD. Due to prominent neuropsychological deficits and worse seizure outcome, treatment strategies in FCD type I are more challenging than previously reported and these children should be recognized and specifically addressed within the incoherent group of patients with malformative brain disorders.
Clinic for Neurosurgery and Neuroradiology Behandlungszentrum Vogtareuth Vogtareuth Germany
Department of Radiology Olgahospital Stuttgart Stuttgart Germany
Epilepsy Center Department of Neurology University Hospital Erlangen Erlangen Germany
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- $a Kršek, Pavel, $d 1972- $7 xx0061338 $u Department of Pediatric Neurology, Charles University, Second Medical School, Motol Hospital, Prague, Czech Republic
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- $a Different presurgical characteristics and seizure outcomes in children with focal cortical dysplasia type I or II / $c Pavel Krsek, Tom Pieper, Anja Karlmeier, Michelle Hildebrandt, Dieter Kolodziejczyk, Peter Winkler, Elisabeth Pauli, Ingmar Blümcke and Hans Holthausen
- 314 __
- $a Department of Pediatric Neurology, Charles University, Second Medical School, Motol Hospital, Prague, Czech Republic. pavel.krsek@post.cz
- 520 9_
- $a PURPOSE: Cortical dysplasia (FCD) is a frequent cause of epilepsy in childhood. Two major pathological variants are distinguished, FCD type I and II. The aim of the study was to characterize differences between FCD type I and II with respect to imaging and EEG findings, clinical and neuropsychological presentations, and surgical outcome. METHODS: Forty children with refractory epilepsy and histopathologically confirmed FCD were retrospectively analyzed. FCD type I was identified in 24 and FCD type II in 16 patients. RESULTS: Characteristic MRI abnormalities in FCD type I included subtle white matter signal changes and regional reduction of the white matter volume. Typical MRI findings in FCD type II were increased cortical thickness, transmantle sign, gray-white matter junction blurring, fluid-attenuated inversion recovery (FLAIR) and proton density (PD) gray matter signal changes as well as T1w, and PD white matter signal changes. Continuous EEG slowing was significantly more common in patients with FCD type I. Children with FCD type I presented with lower levels of intelligence and were suffering more often from maladaptive behavior and behavioral disorders. Surgical outcome was significantly worse in the FCD type I group (seizure freedom was achieved in 21% FCD type I patients and in 75% FCD type II subjects, p < 0.001). CONCLUSIONS: Clinically important differences were found in children with distinct histopathological subtypes of FCD. Due to prominent neuropsychological deficits and worse seizure outcome, treatment strategies in FCD type I are more challenging than previously reported and these children should be recognized and specifically addressed within the incoherent group of patients with malformative brain disorders.
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- $a elektroencefalografie $7 D004569
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- $a ženské pohlaví $7 D005260
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- $a fluorodeoxyglukosa F18 $x diagnostické užití $7 D019788
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- $a gliový fibrilární kyselý protein $x metabolismus $7 D005904
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- $a Pieper, Tom $u Epilepsy-Center for Children, Neuropediatric Clinic and Clinic for Neurorehabilitation, Behandlungszentrum Vogtareuth, Vogtareuth, Germany
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- $a Karlmeier, Aanja $u Epilepsy-Center for Children, Neuropediatric Clinic and Clinic for Neurorehabilitation, Behandlungszentrum Vogtareuth, Vogtareuth, Germany
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- $a Hildebrandt, Michelle $u Department of Neuropathology and Neuropathological Reference Center for Epilepsy Surgery, University Hospital Erlangen, Erlangen, Germany
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- $a Kolodziejczyk, Dieter $u Clinic for Neurosurgery and Neuroradiology, Behandlungszentrum Vogtareuth, Vogtareuth, Germany
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- $a Winkler, Peter $u Department of Radiology, Olgahospital Stuttgart, Stuttgart, Germany
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- $a Pauli, Elisabeth $u Epilepsy Center, Department of Neurology, University Hospital Erlangen, Erlangen, Germany
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- $a Blümcke, Ingmar $u Department of Neuropathology and Neuropathological Reference Center for Epilepsy Surgery, University Hospital Erlangen, Erlangen, Germany
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- $a Holthausen, Hans $u Epilepsy-Center for Children, Neuropediatric Clinic and Clinic for Neurorehabilitation, Behandlungszentrum Vogtareuth, Vogtareuth, Germany
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- $t Epilepsia $w MED00001567 $g Roč. 50, č. 1 (2009), s. 125-137
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- $a 3
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- $a NR8843 $p MZ0
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- $a 2011-1B09/dkme