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Case report

New Onset Epilepsia Partialis Continua Presenting as Complex Visual Hallucinations associated with Voltage-Gated Potassium Channel Antibody

admission and showed a focal abnormality involving the visual cortex, calcarine region, as well as the more inferior occipital lobe and posterior temporal lobe on the right, with enhancement, FLAIR hyperintensity, but only minimal diffusion asymmetry. On Day 7 of admission, given the lack of response to multiple antiepileptic drugs, negative lumbar puncture, and worsening MRI findings, the patient was started on methylprednisolone 1 gram IV x 3 days for presumed autoimmune encephalitis. Minimal

Svetlana P. Eckert, Ping Li

North American Journal of Medicine and Science , ISSUE 1, 28–33

Case report

Adolescent with acute psychosis due to anti-N-methyl-D-aspartate receptor encephalitis: successful recovery

include leucine-rich glioma inactivated 1 (LGI1), contactin-associated protein-2 (CASPR2), and other proteins (9). The clinical characteristics of encephalitis, such as seizures, memory loss, sleep disturbance, as well as laboratory findings of hyponatremia, inflammatory cerebrospinal fluid (CSF), temporal lobe abnormalities on magnetic resonance imaging (MRI), and abnormal electroencephalography (EEG) have been previously described (10). A case of autoimmune encephalitis seropositive for NMDAR and

Dovile Jonuskaite, Paulius Kalibatas, Ruta Praninskiene, Asta Zalubiene, Aurelija Jucaite, Rimante Cerkauskiene

Scandinavian Journal of Child and Adolescent Psychiatry and Psychology , ISSUE 3, 111–115

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