dc.contributor.author |
Feghiu, Ludmila |
|
dc.contributor.author |
Hadjiu, Svetlana |
|
dc.contributor.author |
Calcii, Cornelia |
|
dc.contributor.author |
Sprincean, Mariana |
|
dc.contributor.author |
Lupușor, Nadejda |
|
dc.contributor.author |
Griu, Corina |
|
dc.contributor.author |
Cuznet, Ludmila |
|
dc.contributor.author |
Racovita, Stela |
|
dc.contributor.author |
Groppa, Stanislav |
|
dc.date.accessioned |
2021-10-07T13:33:10Z |
|
dc.date.available |
2021-10-07T13:33:10Z |
|
dc.date.issued |
2021 |
|
dc.identifier.citation |
FEGHIU, Ludmila, HADJIU, Svetlana, CALCII, Cornelia, SPRINCEAN, Mariana, LUPUSOR, Nadejda, et al. Drug-resistant epilepsies in children: clinical case. In: The Moldovan Medical Journal. 2021, vol. 64, no 3 (Neuro Congress Issue), p. 40. ISSN 2537-6381. |
|
dc.identifier.uri |
http://repository.usmf.md/handle/20.500.12710/18106 |
|
dc.description.abstract |
Background: Refractory epilepsy is estimated to affect 10-20% of children diagnosed with epilepsy. The impact of drug-resistant epilepsy can
have a profound effect on education abilities, cognitive functioning presiding over intellectual disabilities, psychiatric comorbidity, physical
injury, sudden death in epilepsy and poor quality of life. Various predictors of drug resistance have been identified; however, the exact prediction
factor remains a challenge. The aim of the study is to present a case of drug-resistant epilepsy case with polymorphic seizures and various
electroencephalographic video patterns.
Material and methods: observational study of the clinical case of drug resistance in children.
Results: The clinical case of the child with drug-resistant epilepsy, manifested by polymorphism crisis was confirmed by the video EEG monitoring.
The 3.0T brain MRI epilepsy protocol revealed the structural thinning of the white matter of the cerebral hemispheres, periventricular cystic defects
and diffuse periventricular gliosis changes with diffuse enlargement of the ventricular and cisternae cerebral systems and bilateral reduction of
hippocampal areas, atrophic type. Treatment of the child included ACTH, Valproic acid, Levetiracetam, Perampanel, but freedom from seizures
was not achieved. The prognosis remained reserved.
Conclusions: despite the antiepileptic drug treatment performed according to ILAE guidelines, the child continues to develop polymorphic
epileptic seizures. The drug-resistant epilepsy is dependent on the child’s age, type of seizures, electroencephalographic appearance, the presence
of structural changes in the brain. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
The Scientific Medical Association of the Republic of Moldova |
en_US |
dc.relation.ispartof |
The Moldovan Medical Journal |
en_US |
dc.subject |
drug-resistant |
en_US |
dc.subject |
epilepsy |
en_US |
dc.subject |
child |
en_US |
dc.subject |
refractory epilepsy |
en_US |
dc.title |
Drug-resistant epilepsies in children: clinical case |
en_US |
dc.type |
Other |
en_US |