Purpose: The method of temporal lobectomy and parietooccipital disconnection has been applied in the treatment of patients with monolateral widespread cortical lesions and with hand motor function intact. There are no data regarding the use of this method in the treatment of patients with bilateral lesions.
Case Report: A case history of a 15-year-old female patient with medically refractory epilepsy is presented. Magnetic resonance imaging revealed bilateral periventricular nodular heterotopia associated with cortical dysplasia (CD) in the right temporo-parietal region. The left hemisphere had no signs of CD. Invasive monitoring revealed rhythmic theta-delta activity during the interictal period and fast activity during the ictal onset in the right temporal and parietal regions. The surgery procedure consisted of anterior temporal lobectomy, the removal of the right heterotopy nodus, the dissection of the posterior part of the corpus callosum, and the detachment of the temporo-parieto-occipital complex by dissection behind the sensorimotor cortex. Histological examination of the cortex revealed CD type I. The patient has been seizure-free for 4 years after surgery.
Conclusion: Partial disconnection procedures may be effective in cases where total hemispherotomy is not indicated in patients with bilateral lesions and a well-lateralized epileptogenic zone localized in the temporo-parieto-occipital region.
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http://dx.doi.org/10.1016/j.ebcr.2013.02.002 | DOI Listing |
Int J Surg Case Rep
December 2024
Pediatric Ophthalmic Pathology Department, SI "The Filatov Institute of Eye Diseases and Tissue Therapy of the NAMS of Ukraine", 49/51 Frantsuzkyi Bulvar, Odesa 65015, Ukraine.
Introduction: Idiopathic congenital acorea is extremely rare. There are several techniques for preserving the clear lens during pupil formation.
Case Presentation: The complete pupil absence caused acute glaucoma attack 2 weeks after birth, which was controlled in a 1-month-old child by peripheral iridectomy and disconnecting iris-corneal synechias.
Cogn Neurodyn
October 2024
School of Information Technology Engineering, Tianjin University of Technology and Education, Tianjin, 300350 China.
Alzheimer's Disease (AD) is a neurodegenerative disorder characterized by energy diffusion and partial disconnection in the brain, with its main feature being an insidious onset and subtle clinical symptoms. Electroencephalogram (EEG) as a primary tool for assessing and aiding in the diagnosis of brain diseases has been widely used in AD detection. Accurate diagnosis is crucial for preventing the transition from early cognitive impairment to AD and providing early treatment for AD patients.
View Article and Find Full Text PDFSci Rep
October 2024
Department of Data Science and Computer Applications, Manipal Institute of Technology, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India.
Self-Compacting Concrete (SCC) allows for the use of non-desalted sea sand as a fine aggregate, but the durability of triple mix SCC with partial sea sand replacement remains unclear. To optimize binder and fine aggregate replacements, tests for consistency, setting times, soundness, compressive strength, and Ultrasonic Pulse Velocity were performed. Six SCC variations, incorporating 30 Class F Fly Ash (FA), 5 Ground Granulated Blast Furnace Slag (GGBS), and various fine aggregate combinations, were evaluated for their fresh, mechanical, microstructural, and durability properties.
View Article and Find Full Text PDFNeurocrit Care
September 2024
Division of Anesthesia, Pain Management and Intensive Care, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Background: The apnea test (AT) plays a vital role in diagnosing brain death by evaluating the absence of spontaneous respiratory activity. It entails disconnecting the patient from mechanical ventilation to raise the CO partial pressure and lower the pH. Occasionally, the AT is aborted because of safety concerns, such as hypoxemia and hemodynamic instability, to prevent worsening conditions.
View Article and Find Full Text PDFMalformation of cortical development is an important cause of drug-resistant epilepsy in young children. Mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) has been added to the last focal cortical dysplasia (FCD) classification and commonly involves the frontal lobe. The semiology at the onset of epilepsy is dominated by non-lateralizing infantile spasm; the boundaries of the malformation are usually difficult to determine by magnetic resonance imaging (MRI) and positron emission tomography (PET), and electroencephalography (EEG) findings are often widespread.
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