Panayiotopoulos syndrome with convulsive status epilepticus at the onset: A long-term study

• Published in: Seizure (London, England) Vol. 23; no. 9; pp. 728 - 731
• Main Authors: Verrotti, Alberto, Sebastiani, Marianna, Giordano, Lucio, Striano, Pasquale, Belcastro, Vincenzo, Franzoni, Emilio, Parisi, Pasquale, Pruna, Dario, Spalice, Alberto, Vignoli, Aglaia, Grosso, Salvatore
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.10.2014
• Subjects: Adolescent; Anticonvulsants - therapeutic use; Child; Child, Preschool; Convulsive status epilepticus; Electroencephalography; Epilepsy, Rolandic - diagnosis; Epilepsy, Rolandic - etiology; Epilepsy, Rolandic - therapy; Female; Humans; Longitudinal Studies; Male; Neurology; Occipital spikes; Panayiotopoulos syndrome, Generalized clonic seizures; Phenytoin - therapeutic use; Retrospective Studies; Status Epilepticus - complications; Panayiotopoulos syndrome, Generalized clonic seizures; Convulsive status epilepticus; Occipital spikes
• ISSN: 1059-1311; 1532-2688; 1532-2688
• DOI: 10.1016/j.seizure.2014.05.013

•We describe 37 cases of Convulsive Status Epilepticus at the onset of Panayiotopoulos syndrome.•We compare them with a group of children who have experienced classic autonomic signs of PS.•Convulsive Status Epilepticus is not an event so rare of Panayiotopoulos syndrome.•The type of onset does not correlate with the prognosis. To better define the convulsive status epilepticus (CSE) as a possible manifestation at the onset of Panayiotopoulos syndrome (PS) and to assess its prognostic value in these children. Children with CSE and diagnostic criteria of PS were identified, followed clinically and compared with a group of patients with PS without CSE from 1993 to 2012. We identified 37 patients with CSE at the onset of PS. During the same period we identified 72 children with autonomic symptoms of PS without CSE. The first episode of CSE occurred at a mean age of 6.5 years. Generalized clonic seizures were the most common ictal event and one-third of the patients required admission to Intensive Care Units. Interictal EEGs showed occipital spike activity in 31 (83.7%) subjects. Only 14 (37.8%) patients were treated with valproic acid and for two of them (5.40%) it was necessary to administer other drugs. There were no intractable cases. The overall prognosis was excellent. After the first event, 15 subjects (40.54%) experienced at least another typical PS seizure, but all patients were seizure free at the last follow-up. CSE is not uncommon in PS and it may occur at the onset of benign childhood epilepsy, without leading to a poor prognosis.