Focal Cortical Dysplasia with hippocampal sclerosis.
Devendra JadavVaibhav GuptaSudeep KheraVikas P MeshramPublished in: Autopsy & case reports (2023)
Focal Cortical Dysplasia (FCD) is a group of focal developmental malformations of the cerebral cortex cytoarchitecture. FCD usually manifests as medically intractable epilepsy, especially in young children. Live patients are diagnosed by radiological examination such as magnetic resonance imaging (MRI), fluorodeoxyglucose positron emission tomography (FDG PET), magnetoencephalography (MEG), diffusion-tensor imaging (DTI), and intracranial electroencephalogram (EEG). While some cases can be missed by radiological examination, they are usually diagnosed on the histopathological examination of the surgically removed specimens of medically intractable epilepsy patients. We report a case of a young girl with cerebral palsy, mental retardation, and seizure disorder who died in her sleep. The deceased was diagnosed with FCD type III with hippocampal sclerosis on histopathological examination at autopsy. H & E stain and NeuN immunohistochemistry neuronal cell marker were used to demonstrate the findings of FCD.
Keyphrases
- cerebral ischemia
- positron emission tomography
- computed tomography
- magnetic resonance imaging
- end stage renal disease
- pet ct
- ejection fraction
- newly diagnosed
- pet imaging
- chronic kidney disease
- cerebral palsy
- peritoneal dialysis
- type iii
- single cell
- stem cells
- contrast enhanced
- mesenchymal stem cells
- temporal lobe epilepsy
- working memory
- bone marrow
- high density