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Benign convulsions in children with mild gastroenteritis
Luca Castellazzi1, Nicola Principi1, Carlo Agostoni2
1Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Insights
Benign convulsions with mild gastroenteritis (CwG) is a recognized epileptic syndrome in children. Understanding CwG characteristics helps avoid unnecessary treatments and hospitalizations for this benign condition.
Area of Science:
- Pediatric Neurology
- Epileptology
- Infectious Diseases
Background:
- Benign convulsions with mild gastroenteritis (CwG) is a condition in children with convulsions and mild gastroenteritis, often without fever.
- CwG has not been fully recognized as an epileptic syndrome, with its pathogenesis remaining unclear.
Purpose of the Study:
- To review and synthesize current knowledge on CwG.
- To facilitate the recognition and appropriate treatment of CwG.
Main Methods:
- Literature review of CwG cases.
- Analysis of clinical presentation, diagnostic findings, and treatment outcomes.
Main Results:
- CwG shares clinical and prognostic similarities with febrile seizures.
- Occurs in children aged 1 month to 3 years, often during winter/spring with viral gastroenteritis (rotavirus, norovirus).
- Seizures are typically focal on ictal EEG, despite generalized tonic-clonic description; standard diagnostics (EEG, LP, imaging) are usually normal.
Conclusions:
- Knowledge of CwG is crucial for pediatricians to prevent unnecessary hospitalizations and investigations.
- Avoiding unnecessary drug administration is important due to potential side effects.
Background:
Benign convulsions with mild gastroenteritis (CwG) is a clinical condition characterized by convulsions occurring in otherwise healthy children, usually in the absence of fever and in the presence of mild acute gastroenteritis. Until now, CwG had not been fully recognized as an epileptic syndrome, and several aspects of this condition are not clearly defined, especially its pathogenesis.
Methods:
The main aim of this paper is to discuss after the review of the literature what is known about CwG to facilitate its recognition and treatment.
Results:
CwG is a benign condition that has several clinical and prognostic similarities with febrile seizures. The disease occurs in infants and in children who are 1 month to 3 years old, during the winter and early spring when rotavirus and norovirus are circulating. In most cases, seizures follow gastrointestinal symptoms. In a minority of patients, the seizures and gastrointestinal symptoms occur before or simultaneously with the development of diarrhoea. Even if convulsions are mostly described as generalized tonic-clonic, the ictal recordings have always demonstrated a focal origin. Electroencephalography, lumbar punctures, and radiological examinations are not useful because they are normal in these patients; and when alterations are present, they disappear in a relatively short time. Only prolonged seizures, which are usually not common, require antiepileptic treatments in the acute phase.
Conclusion:
Knowledge of CwG characteristics is essential for paediatricians to avoid useless hospitalization, examinations and, above all, drug administration, as the drugs have potential side effects.
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