keyword
https://read.qxmd.com/read/38187332/cortical-surface-analysis-for-focal-cortical-dysplasia-diagnosis-by-using-pet-images
#21
JOURNAL ARTICLE
Eric Jacob Bacon, Chaoyang Jin, Dianning He, Shuaishuai Hu, Lanbo Wang, Han Li, Shouliang Qi
Focal cortical dysplasia (FCD) is a neurological disorder distinguished by faulty brain cell structure and development. Repetitive and uncontrollable seizures may be linked to FCD's aberrant cortical thickness, gyrification, and sulcal depth. Quantitative cortical surface analysis is a crucial alternative to ineffective visual inspection. This study recruited 42 subjects including 22 FCD patients who underwent surgery and 20 healthy controls (HC). For the FCD patients, T1-weighted and PET images were obtained by a PET-MRI scanner, and the confirmed epileptogenic zone (EZ) was collected from postsurgical follow-up...
January 15, 2024: Heliyon
https://read.qxmd.com/read/38182838/-18-f-synvest-1-and-18-f-fdg-quantitative-pet-imaging-in-the-presurgical-evaluation-of-mri-negative-children-with-focal-cortical-dysplasia-type-ii
#22
JOURNAL ARTICLE
Ling Xiao, Jinhui Yang, Haoyue Zhu, Ming Zhou, Jian Li, Dingyang Liu, Yongxiang Tang, Li Feng, Shuo Hu
PURPOSE: MRI-negative children with focal cortical dysplasia type II (FCD II) are one of the most challenging cases in surgical epilepsy management. We aimed to utilize quantitative positron emission tomography (QPET) analysis to complement [18 F]SynVesT-1 and [18 F]FDG PET imaging and facilitate the localization of epileptogenic foci in pediatric MRI-negative FCD II patients. METHODS: We prospectively enrolled 17 MRI-negative children with FCD II who underwent [18 F]SynVesT-1 and [18 F]FDG PET before surgical resection...
January 6, 2024: European Journal of Nuclear Medicine and Molecular Imaging
https://read.qxmd.com/read/38167978/good-outcome-of-resective-epilepsy-surgery-in-a-one-year-old-child-with-drug-resistant-focal-epilepsy-with-a-novel-pathogenic-col4a1-mutation
#23
JOURNAL ARTICLE
Nicholas Fearns, Matias Wagner, Ingo Borggräfe, Mathias Kunz, Jan Rémi, Christian Vollmar
Pathogenic variants in COL4A1, encoding the alpha chain of type IV collagen, have been associated with cerebrovascular pathology as well as malformations of cortical development, thereby causing structural epilepsy. This case illustrates successful resective epilepsy surgery in a 12-month-old girl with left occipital focal cortical dysplasia (FCD) associated with a heterozygous splice-donor variant in COL4A1. She presented with drug-resistant focal epilepsy with daily seizures from the age of 2 months, refractory to several combinations of antiseizure medications, as well as mild right-sided hemiparesis and developmental delay...
January 2, 2024: Neuropediatrics
https://read.qxmd.com/read/38148028/correspondence-between-scalp-eeg-and-seeg-seizure-onset-patterns-in-patients-with-mri-negative-drug-resistant-focal-epilepsy
#24
JOURNAL ARTICLE
Anna Bolzan, Jeanne Benoit, Francesca Pizzo, Julia Makhalova, Nathalie Villeneuve, Romain Carron, Didier Scavarda, Fabrice Bartolomei, Stanislas Lagarde
OBJECTIVE: Our objective was to evaluate the relationship between scalp EEG and stereoelectroencephalography (SEEG) seizure onset patterns (SOPs) in patients with MRI-negative drug-resistant focal epilepsy. METHODS: We analysed retrospectively 41 patients without visible lesion on brain MRI who underwent video-EEG followed by SEEG. We defined five types of SOPs on scalp EEG and eight types on SEEG. We examined how various clinical variables affected scalp EEG SOPs...
December 26, 2023: Epilepsia Open
https://read.qxmd.com/read/38116874/epileptogenic-focal-lesions-in-dravet-syndrome-a-warning-to-investigators
#25
JOURNAL ARTICLE
Rita Ventura, Álvaro Beltrán-Corbellini, Rafael Toledano, Irene Sánchez-Miranda Román, Irene García-Morales, Antonio Gil-Nagel
OBJECTIVE: Most patients with Dravet syndrome (DS) have unremarkable neuroimaging studies. However, a small number of patients exhibit focal abnormalities that may modify the epilepsy phenotype. We report a case series of DS patients carrying SCN1A variants concurrent with additional focal brain lesions, aiming to provide details regarding their clinical course, electrographic findings, and imaging features. METHODS: We reviewed the electronic medical records of patients with developmental and epileptic encephalopathies in our center, from January 2000 to December 2022, identifying 90 patients with DS resulting from SCN1A variants...
December 20, 2023: Epileptic Disorders: International Epilepsy Journal with Videotape
https://read.qxmd.com/read/38106257/metabolic-heterogeneity-in-different-subtypes-of-malformations-of-cortical-development-causing-epilepsy-a-proton-magnetic-resonance-spectroscopy-study
#26
JOURNAL ARTICLE
Huaxia Pu, Liping Wang, Wenyu Liu, Qiaoyue Tan, Xinyue Wan, Weina Wang, Xiaorui Su, Huaiqiang Sun, Simin Zhang, Qiang Yue, Qiyong Gong
BACKGROUND: The most common subtypes of malformations of cortical development (MCDs) are gray matter heterotopia (GMH), focal cortical dysplasia (FCD), and polymicrogyria (PMG). This study aimed to characterize the possible neurometabolic abnormalities and heterogeneity in different MCDs subtypes using proton magnetic resonance spectroscopy (1 H-MRS). METHODS: In this prospective cross-sectional study, we recruited 29 patients with MCDs and epilepsy, including ten with GMH, ten with FCD, and nine with PMG, as well as 25 age- and sex-matched healthy controls (HC) from the Epilepsy Center of West China Hospital of Sichuan University between August 2018 and November 2021...
December 1, 2023: Quantitative Imaging in Medicine and Surgery
https://read.qxmd.com/read/38093325/the-impact-of-referring-patients-with-drug-resistant-focal-epilepsy-to-an-epilepsy-center-for-presurgical-diagnosis
#27
JOURNAL ARTICLE
Leonhard Mann, Felix Rosenow, Adam Strzelczyk, Elke Hattingen, Laurent M Willems, Patrick N Harter, Katharina Weber, Catrin Mann
BACKGROUND: Epilepsy surgery is an established treatment for drug-resistant focal epilepsy (DRFE) that results in seizure freedom in about 60% of patients. Correctly identifying an epileptogenic lesion in magnetic resonance imaging (MRI) is challenging but highly relevant since it improves the likelihood of being referred for presurgical diagnosis. The epileptogenic lesion's etiology directly relates to the surgical intervention's indication and outcome. Therefore, it is vital to correctly identify epileptogenic lesions and their etiology presurgically...
December 14, 2023: Neurological research and practice
https://read.qxmd.com/read/38082811/identification-of-seizure-onset-zone-from-intracranial-eeg-using-source-selection-based-domain-adaptation
#28
JOURNAL ARTICLE
Keisuke Matsubayashi, Yasushi Iimura, Takumi Mitsuhashi, Hidenori Sugano, Kosuke Fukumori, Xuyang Zhao, Toshihisa Tanaka
For focal epilepsy patients, correctly identifying the seizure onset zone (SOZ) is essential for surgical treatment. In automated realistic SOZ identification, it is necessary to identify the SOZ of an unknown patient using another patient's electroencephalogram (EEG). However, in such cases, the influence of individual differences in EEG becomes a bottleneck. In this paper, we propose the method with domain adaptation and source patient selection to address the issue of individual differences in EEG and improve performance...
July 2023: Annual International Conference of the IEEE Engineering in Medicine and Biology Society
https://read.qxmd.com/read/38077172/evaluation-of-cognitive-impairment-in-refractory-temporal-lobe-epilepsy-patients-concerning-structural-brain-lesions
#29
JOURNAL ARTICLE
Farinaz Tabibian, Jafar Mehvari Habibabadi, Mohammad Reza Maracy, Hossein Kahnouji, Mahtab Rahimi, Maryam Rezaei
INTRODUCTION: Temporal lobe epilepsy (TLE) is the most prevalent form of drug-resistant epilepsy with concurrent cognitive impairment. Prevention, earlier diagnosis, and personalized management of cognitive deficits in TLE require more understanding of underlying structural and functional brain Ialterations. No study has evaluated the performance of TLE patients in different cognitive domains based on their structural brain lesions. METHODS: In this study, 69 refractory TLE patients underwent magnetic resonance imaging (MRI) epilepsy protocol and several neuropsychological tests, consisting of the Wechsler adult intelligence scale-revised, Rey-Osterrieth complex figure test, verbal fluency test, digit span test, spatial span test, Wechsler memory scale-III, design fluency test, Rey visual design learning test, auditory-verbal learning test, and trail making test...
2023: Basic and Clinical Neuroscience
https://read.qxmd.com/read/38070410/epileptogenesis-and-drug-resistant-in-focal-cortical-dysplasias-update-on-clinical-cellular-and-molecular-markers
#30
REVIEW
Daniel Rodrigo Marinowic, Douglas Bottega Pazzin, Sofia Prates da Cunha de Azevedo, Giulia Pinzetta, João Victor Machado de Souza, Fernando Tonon Schneider, Thales Thor Ramos Previato, Fábio Jean Varella de Oliveira, Jaderson Costa Da Costa
Focal cortical dysplasia (FCD) is a cortical malformation in brain development and is considered as one of the major causes of drug-resistant epilepsiesin children and adults. The pathogenesis of FCD is yet to be fully understood. Imaging markers such as MRI are currently the surgeons major obstacle due to the difficulty in delimiting the precise dysplasic area and a mosaic brain where there is epileptogenic tissue invisible to MRI. Also increased gene expression and activity may be responsible for the alterations in cell proliferation, migration, growth, and survival...
January 2024: Epilepsy & Behavior: E&B
https://read.qxmd.com/read/38033536/enhanced-focal-cortical-dysplasia-detection-in-pediatric-frontal-lobe-epilepsy-with-asymmetric-radiomic-and-morphological-features
#31
JOURNAL ARTICLE
Manli Zhang, Hao Yu, Gongpeng Cao, Jinguo Huang, Yanzhu Lu, Jing Zhang, Nana Liu, Wenjing Zhang, Yintao Cheng, Guixia Kang, Lixin Cai
OBJECTIVE: Focal cortical dysplasia (FCD) is the most common pathological cause for pediatric epilepsy, with frontal lobe epilepsy (FLE) being the most prevalent in the pediatric population. We attempted to utilize radiomic and morphological methods on MRI and PET to detect FCD in children with FLE. METHODS: Thirty-seven children with FLE and 20 controls were included in the primary cohort, and a five-fold cross-validation was performed. In addition, we validated the performance in an independent site of 12 FLE children...
2023: Frontiers in Neuroscience
https://read.qxmd.com/read/38014782/advances-in-neuroimaging-and-multiple-post-processing-techniques-for-epileptogenic-zone-detection-of-drug-resistant-epilepsy
#32
REVIEW
Lei Yao, Nan Cheng, An-Qiang Chen, Xun Wang, Ming Gao, Qing-Xia Kong, Yu Kong
Among the approximately 20 million patients with drug-resistant epilepsy (DRE) worldwide, the vast majority can benefit from surgery to minimize seizure reduction and neurological impairment. Precise preoperative localization of epileptogenic zone (EZ) and complete resection of the lesions can influence the postoperative prognosis. However, precise localization of EZ is difficult, and the structural and functional alterations in the brain caused by DRE vary by etiology. Neuroimaging has emerged as an approach to identify the seizure-inducing structural and functional changes in the brain, and magnetic resonance imaging (MRI) and positron emission tomography (PET) have become routine noninvasive imaging tools for preoperative evaluation of DRE in many epilepsy treatment centers...
November 28, 2023: Journal of Magnetic Resonance Imaging: JMRI
https://read.qxmd.com/read/37964137/characterisation-of-a-novel-18-f-fdg-brain-pet-database-and-combination-with-a-second-database-for-optimising-detection-of-focal-abnormalities-using-focal-cortical-dysplasia-as-an-example
#33
JOURNAL ARTICLE
Sameer Omer Jin, Inés Mérida, Ioannis Stavropoulos, Robert D C Elwes, Tanya Lam, Eric Guedj, Nadine Girard, Nicolas Costes, Alexander Hammers
BACKGROUND: Brain [18 F]FDG PET is used clinically mainly in the presurgical evaluation for epilepsy surgery and in the differential diagnosis of neurodegenerative disorders. While scans are usually interpreted visually on an individual basis, comparison against normative cohorts allows statistical assessment of abnormalities and potentially higher sensitivity for detecting abnormalities. Little work has been done on out-of-sample databases (acquired differently to the patient data). Combination of different databases would potentially allow better power and discrimination...
November 15, 2023: EJNMMI Research
https://read.qxmd.com/read/37948689/localized-focal-cortical-dysplasia-type-ii-seizure-freedom-with-lesionectomy-guided-by-mri-and-fdg-pet
#34
JOURNAL ARTICLE
Naotaka Usui, Akihiko Kondo, Kazumi Matsuda, Hiroshi Ogawa, Takuji Nishida, Kentaro Tokumoto, Norihiko Kawaguchi, Takashi Matsudaira, Yasukiyo Araki, Masataka Fukuoka, Hirowo Omatsu, Hideyuki Otani, Tokito Yamaguchi, Katsumi Imai, Yukitoshi Takahashi
OBJECTIVE: The authors perform thorough, noninvasive presurgical evaluations for intractable epilepsy at their center and avoid unnecessary intracranial EEG when possible. The purpose of this study was to clarify the appropriateness of their lesion-oriented surgical strategy for localized focal cortical dysplasia (FCD) type II. METHODS: Fifty-one patients with pathologically proven localized FCD type II who were followed for at least 1 year after surgery were included...
November 10, 2023: Journal of Neurosurgery
https://read.qxmd.com/read/37946310/deep-histopathology-genotype-phenotype-analysis-of-focal-cortical-dysplasia-type-ii-differentiates-between-the-gator1-altered-autophagocytic-subtype-iia-and-mtor-altered-migration-deficient-subtype-iib
#35
JOURNAL ARTICLE
Jonas Honke, Lucas Hoffmann, Roland Coras, Katja Kobow, Costin Leu, Tom Pieper, Till Hartlieb, Christian G Bien, Friedrich Woermann, Thomas Cloppenborg, Thilo Kalbhenn, Ahmed Gaballa, Hajo Hamer, Sebastian Brandner, Karl Rössler, Arnd Dörfler, Stefan Rampp, Johannes R Lemke, Sara Baldassari, Stéphanie Baulac, Dennis Lal, Peter Nürnberg, Ingmar Blümcke
Focal cortical dysplasia type II (FCDII) is the most common cause of drug-resistant focal epilepsy in children. Herein, we performed a deep histopathology-based genotype-phenotype analysis to further elucidate the clinico-pathological and genetic presentation of FCDIIa compared to FCDIIb. Seventeen individuals with histopathologically confirmed diagnosis of FCD ILAE Type II and a pathogenic variant detected in brain derived DNA whole-exome sequencing or mTOR gene panel sequencing were included in this study...
November 9, 2023: Acta Neuropathologica Communications
https://read.qxmd.com/read/37943122/a-5-year-old-boy-with-super-refractory-status-epilepticus-and-ranbp2-variant-warranting-life-saving-hemispherotomy
#36
JOURNAL ARTICLE
Barbora Straka, Miroslav Koblížek, Barbora Heřmanovská, Radka Valkovičová, Lenka Krsková, Markéta Kalinová, Markéta Vlčková, Josef Zámečník, Petra Laššuthová, Lucie Sedláčková, David Staněk, Alice Maulisová, Michal Tichý, Martin Kynčl, Pavel Kršek
Focal cortical dysplasia (FCD) represents the most common cause of drug-resistant epilepsy in adult and pediatric surgical series. However, genetic factors contributing to severe phenotypes of FCD remain unknown. We present a patient with an exceptionally rapid development of drug-resistant epilepsy evolving in super-refractory status epilepticus. We performed multiple clinical (serial EEG, MRI), biochemical (metabolic and immunological screening), genetic (WES from blood- and brain-derived DNA) and histopathological investigations...
November 9, 2023: Epilepsia Open
https://read.qxmd.com/read/37939785/the-clinical-imaging-pathological-and-genetic-landscape-of-bottom-of-sulcus-dysplasia
#37
JOURNAL ARTICLE
Emma Macdonald-Laurs, Aaron E L Warren, Peter Francis, Simone A Mandelstam, Wei Shern Lee, Matthew Coleman, Sarah E M Stephenson, Sarah Barton, Colleen D'Arcy, Paul J Lockhart, Richard J Leventer, A Simon Harvey
Bottom-of-sulcus dysplasia (BOSD) is increasingly recognised as a cause of drug-resistant, surgically-remediable, focal epilepsy, often in seemingly MRI-negative patients. We describe the clinical manifestations, morphological features, localisation patterns, and genetics of BOSD, with the aims of improving management and understanding pathogenesis. We studied 85 patients with BOSD diagnosed between 2005-2022. Presenting seizure and EEG characteristics, clinical course, genetic findings, and treatment response were obtained from medical records...
November 6, 2023: Brain
https://read.qxmd.com/read/37907727/yield-of-non-invasive-imaging-in-mri-negative-focal-epilepsy
#38
JOURNAL ARTICLE
Christian Czarnetzki, Laurent Spinelli, Hans-Jürgen Huppertz, Karl Schaller, Shahan Momjian, Johannes Lobrinus, Maria-Isabel Vargas, Valentina Garibotto, Serge Vulliemoz, Margitta Seeck
OBJECTIVE: The absence of MRI-lesion reduces considerably the probability of having an excellent outcome (International League Against Epilepsies [ILAE] class I-II) after epilepsy surgery. Surgical success in magnetic-resonance imaging (MRI)-negative cases relies therefore mainly on non-invasive techniques such as positron-emission tomography (PET), subtraction ictal/inter-ictal single-photon-emission-computed-tomography co-registered to MRI (SISCOM), electric source imaging (ESI) and morphometric MRI analysis (MAP)...
November 1, 2023: Journal of Neurology
https://read.qxmd.com/read/37900727/language-lateralization-mapping-reversibly-masked-by-non-dominant-focal-epilepsy-a-case-report
#39
Belén Abarrategui, Valeria Mariani, Michele Rizzi, Luca Berta, Pina Scarpa, Flavia Maria Zauli, Silvia Squarza, Paola Banfi, Piergiorgio d'Orio, Francesco Cardinale, Maria Del Vecchio, Fausto Caruana, Pietro Avanzini, Ivana Sartori
Language lateralization in patients with focal epilepsy frequently diverges from the left-lateralized pattern that prevails in healthy right-handed people, but the mechanistic explanations are still a matter of debate. Here, we debate the complex interaction between focal epilepsy, language lateralization, and functional neuroimaging techniques by introducing the case of a right-handed patient with unaware focal seizures preceded by aphasia, in whom video-EEG and PET examination suggested the presence of focal cortical dysplasia in the right superior temporal gyrus, despite a normal structural MRI...
2023: Frontiers in Human Neuroscience
https://read.qxmd.com/read/37900524/bridging-development-and-disruption-comprehensive-insights-into-focal-cortical-dysplasia-and-epileptic-management
#40
REVIEW
Syed Naveed Mohsin, Han Grezenko, Saadia Khan, Filagot D Eshete, Shraddha Shrestha, Muhammad Kamran, Maryam Affaf, Ayat Jama, Rayan W Gasim, Dewan Zubaer Ahmad, Indresh Yadav, Sidra Arif, Anil K C, Abdul Saboor Khaliq
Focal cortical dysplasia (FCD) is a prominent neurological disorder characterized by disruptions in localized brain cell organization and development. This narrative review delineates the multi-faceted nature of FCD, emphasizing its correlation with drug-resistant epilepsy, predominantly in children and young adults. We explore the historical context of FCD, highlighting its indispensable role in shaping our comprehension of epilepsy and cortical anomalies. The clinical spectrum of FCD is broad, encompassing diverse seizure patterns, cognitive impairments, and associated neuropsychiatric disorders...
September 2023: Curēus
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