Epileptic seizures due to multiple cerebral cavernomatosis

Background. Cavernous angiomas are angiographically occult vascular malformations that are present in 0.4−0.9 % of people, and represent around 5% of all cerebrovascular malformations. They can be single or multiple, and sporadic or familial. The presence of multiple lesions is more frequent in fami...

Full description

Bibliographic Details
Main Authors: Spasić Mirjana, Lukić Stevo
Format: Article
Language:English
Published: Military Health Department, Ministry of Defance, Serbia 2007-01-01
Series:Vojnosanitetski Pregled
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0042-8450/2007/0042-84500707489S.pdf
_version_ 1819053356243484672
author Spasić Mirjana
Lukić Stevo
author_facet Spasić Mirjana
Lukić Stevo
author_sort Spasić Mirjana
collection DOAJ
description Background. Cavernous angiomas are angiographically occult vascular malformations that are present in 0.4−0.9 % of people, and represent around 5% of all cerebrovascular malformations. They can be single or multiple, and sporadic or familial. The presence of multiple lesions is more frequent in familial cavernomatosis. Ten to 30 % are associated with familial clustering. Case report. We presented the case of a 43-year-old man, admitted to the Emergency Department due to unprovoked seizure during the wide awake and everyday activities. Neurological examination was with no focal signs. A 32-channel standard digital EEG was without any significant changes of normal baseline activity. After sleep deprivation EEG showed multifocal, bilateral and asymmetric polyspikes and sharpwaves activity. Hyperventilation induced generalized epileptiform discharges. MRI scan demonstrated multiple small cavernous angiomas. Neuropsychological testing demonstrated a delayed memory impairment. Neurosurgery treatment was not recommended, and the therapy with valproate 1 250 mg/day had an excellent efficacy with no singnificant adverse effects. Conclusion. This patient considered as a rare case with multiple cavernomatosis highlights the importance of neuroradiological examination in adult patients with the first epileptic seizure but with no focal neurological signs. .
first_indexed 2024-12-21T12:34:26Z
format Article
id doaj.art-5802cbf8dd9c4c6b83e6934b734b2092
institution Directory Open Access Journal
issn 0042-8450
language English
last_indexed 2024-12-21T12:34:26Z
publishDate 2007-01-01
publisher Military Health Department, Ministry of Defance, Serbia
record_format Article
series Vojnosanitetski Pregled
spelling doaj.art-5802cbf8dd9c4c6b83e6934b734b20922022-12-21T19:03:57ZengMilitary Health Department, Ministry of Defance, SerbiaVojnosanitetski Pregled0042-84502007-01-0164748949210.2298/VSP0707489SEpileptic seizures due to multiple cerebral cavernomatosisSpasić MirjanaLukić StevoBackground. Cavernous angiomas are angiographically occult vascular malformations that are present in 0.4−0.9 % of people, and represent around 5% of all cerebrovascular malformations. They can be single or multiple, and sporadic or familial. The presence of multiple lesions is more frequent in familial cavernomatosis. Ten to 30 % are associated with familial clustering. Case report. We presented the case of a 43-year-old man, admitted to the Emergency Department due to unprovoked seizure during the wide awake and everyday activities. Neurological examination was with no focal signs. A 32-channel standard digital EEG was without any significant changes of normal baseline activity. After sleep deprivation EEG showed multifocal, bilateral and asymmetric polyspikes and sharpwaves activity. Hyperventilation induced generalized epileptiform discharges. MRI scan demonstrated multiple small cavernous angiomas. Neuropsychological testing demonstrated a delayed memory impairment. Neurosurgery treatment was not recommended, and the therapy with valproate 1 250 mg/day had an excellent efficacy with no singnificant adverse effects. Conclusion. This patient considered as a rare case with multiple cavernomatosis highlights the importance of neuroradiological examination in adult patients with the first epileptic seizure but with no focal neurological signs. .http://www.doiserbia.nb.rs/img/doi/0042-8450/2007/0042-84500707489S.pdfhemangiomacavernouscentral nervous systemepilepsydiagnosisdiagnosis, differentialneurologic examinationelectroencephalographymagnetic resonance spectroscopy
spellingShingle Spasić Mirjana
Lukić Stevo
Epileptic seizures due to multiple cerebral cavernomatosis
Vojnosanitetski Pregled
hemangioma
cavernous
central nervous system
epilepsy
diagnosis
diagnosis, differential
neurologic examination
electroencephalography
magnetic resonance spectroscopy
title Epileptic seizures due to multiple cerebral cavernomatosis
title_full Epileptic seizures due to multiple cerebral cavernomatosis
title_fullStr Epileptic seizures due to multiple cerebral cavernomatosis
title_full_unstemmed Epileptic seizures due to multiple cerebral cavernomatosis
title_short Epileptic seizures due to multiple cerebral cavernomatosis
title_sort epileptic seizures due to multiple cerebral cavernomatosis
topic hemangioma
cavernous
central nervous system
epilepsy
diagnosis
diagnosis, differential
neurologic examination
electroencephalography
magnetic resonance spectroscopy
url http://www.doiserbia.nb.rs/img/doi/0042-8450/2007/0042-84500707489S.pdf
work_keys_str_mv AT spasicmirjana epilepticseizuresduetomultiplecerebralcavernomatosis
AT lukicstevo epilepticseizuresduetomultiplecerebralcavernomatosis