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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/18070
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dc.contributor.authorCondrea, Alexandra
dc.contributor.authorAftene, Daniela
dc.contributor.authorChiosa, Vitalie
dc.contributor.authorGroppa, Stanislav
dc.date.accessioned2021-10-02T19:39:22Z
dc.date.available2021-10-02T19:39:22Z
dc.date.issued2021
dc.identifier.citationCONDREA, Alexandra, AFTENE, Daniela, CHIOSA, Vitalie, GROPPA, Stanislav. Management of brain tumor-related epilepsy: case report. In: The Moldovan Medical Journal. 2021, vol. 64, no 3 (Neuro Congress Issue), p. 28. ISSN 2537-6381.
dc.identifier.issn2537-6381
dc.identifier.issn2537-6373
dc.identifier.urihttp://moldmedjournal.md/wp-content/uploads/2021/09/Congres-Neuro-2021-Spaltul-11.pdf
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/18070
dc.description.abstractBackground: Patients with brain tumor related epilepsy present a complex therapeutic profile and require a unique and multidisciplinary approach. Difficulty in managing epilepsy in patients with brain tumors stems from an overall resistance to medical therapy, frequent interactions between antiepileptic drugs and chemotherapeutic agents, and potential adverse effects of both medical and surgical treatment. Moreover, seizures significantly impact the quality of life, and continued seizures are associated with a poorer outcome. Material and methods: We present the case of a young adult patient with a brain tumor-related epilepsy. Results: A 38-year-old woman was admitted to our hospital with focal motor seizures, with impaired awareness, evolving into bilateral tonicclonic. Her video-electroencephalogram monitoring revealed left temporo-frontal epileptiform discharges, frequently bilateral in wakefulness and sleepiness. Simple and contrasted magnetic resonance of the brain showed a lesion in the left temporal lobe. Patient began taking carbamazepine and levetiracetam, her seizures were partially controlled. A surgical resection was performed, and pathological analysis revealed anaplastic astrocytoma. Post-resection she has had a significant reduction in her seizures, and she is still taking antiepileptic drugs. Conclusions: Patients with refractory epilepsy should be evaluated for potential epilepsy surgery. It is important to identify these patients early to limit the potential morbidity and mortality and to improve their quality of life.en_US
dc.language.isoenen_US
dc.publisherThe Scientific Medical Association of the Republic of Moldovaen_US
dc.relation.ispartofThe Moldovan Medical Journalen_US
dc.subjectbrain tumor-related epilepsyen_US
dc.subjectrefractory epilepsyen_US
dc.subjectanaplastic astrocytomaen_US
dc.titleManagement of brain tumor-related epilepsy: case reporten_US
dc.typeOtheren_US
Appears in Collections:The Moldovan Medical Journal, Vol. 64, No 3, September 2021

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