Article
Cortical dysplasia in a hard-to-control epilepsy case
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Published: | September 11, 2012 |
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Outline
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Objective: To study the histopathological findings in a hard-to-control epilepsy case.
Materials and Methods: We selected a case of a 22-year-old male patient from the National Institute of Neurology and Neurosurgery “Manuel Velasco Suárez”, with hard-to-control epilepsy diagnosis. We revised the clinical history, EEG and MRI studies, and the stereotxis biopsy. The tissues were formalin-fixed, paraffin-embedded, cut into 5–7 µm slices, and stained with hematoxylin-eosin and argentaffin techniques in order to perform photonic microscopy.
Results: EEG report focal mild dysfunction in left temporal and occipital areas. MRI shows dysplasia in temporal and parietal areas with hypointensity on T1 secuence, and hyperintensity on T2 weighted and FLAIR images and polymicrogyric patterns. He was submitted to surgical section of the left parietal cortex; the histopathological study reveals hypoxic areas, difuse microinfarctions, engrossment of the cortical region with eosinophylic neurons, vacuolated neuropil and slight gliosis, and cortical dysplasia.
Conclusions: The cortical dysplasia diagnosis is established. After surgery the patient persists with partial sensitive crisis of the right arm which had remitted with oxcarbazepine 600 mg b.i.d. and levetiracetam 500 mg b.i.d. Currently the patient has a satisfactory evolution with no seizures or any neurological focal signs.
References
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