|
- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2020
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/12076
Title: | Epilepsy in pacients with multiple sclerosis |
Authors: | Ropot, Doina |
Keywords: | multiple sclerosis;epilepsy;seizures;disability |
Issue Date: | 2020 |
Publisher: | MedEspera |
Citation: | ROPOT, Doina. Epilepsy in pacients with multiple sclerosis. In: MedEspera: the 8th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2020, p. 40-41. |
Abstract: | Background. Multiple sclerosis (MS) is a central nervous system disorder characterized by
inflammation, demyelination and neurodegeneration, and is the most common cause of
acquired nontraumatic neurological disability in young adults. The course of the disease varies between individuals: some patients accumulate minimal disability over their lives, whereas
others experience a rapidly disabling disease course. A part of patients with multiple sclerosis
presents also seizures that lead to epilepsy. Several clinical series reported an association
between multiple sclerosis and epilepsy. The most studies show an increased comorbidity
between multiple sclerosis and epilepsy. The cumulative incidence of epilepsy by 10 years after
diagnosis of MS was 1.9%. The probable anatomic basis for the seizures is areas of
inflammation, edema, and/or demyelination in the cerebral cortex and the juxtacortical white
matter generated by a mechanism that is not completely understood; the fact that these plaques
are very common suggests that other factors must operate in view of the rarity of seizures in
MS. In most cases, however, the prognosis of epilepsy was good and there seemed not to be
any clear correlation between the severity of MS and epilepsy.
Case report. A patient V. male, 41 years , came at a neurologist in April 2019 with the
following complaints: facial hyperemia, heat sensations, alterations of consciousness with
convulsive components in the anamnesis. At the same time: walking instability, recurrent
diplopia, frequent urination, sleeping disorders, memory loss and decrease in body mass.
Anamnesis: In 2005 patient has an acute respiratory infection, possible a flu. After a half a year
had appeared diplopia, diplopia and frequent urination. In 2007 the diagnosis of multiple
sclerosis was established. The diagnosis was confirmed in Moscow and the patient started the
treatment with Galatimer acetate (Copaxone) that he administered for 5 years with the
improvement of the evolution of the disease. Subsequently administered Acsoglatiran till
present but without any obvious effect. In 2015 the patient has a seizure for the first time with
unconsciousness but without warning signs. Other signs and symptoms associated with
unconsciousness the patient doesn’t remember. A similar episode was in 2017. In 2019 the
patient received symptomatic treatment in the neurology department for diagnosis: Multiple
sclerosis clinically and imagistic defined, recurrent remissive form, in exacerbation, with
pronounced atactic syndrome. Structural epilepsy-mesial temporal sclerosis on the right
associated to multiple sclerosis plague with focal seizures with bilateral passage treated with
Carbamazepine retard 300 mg/day. Now the antiepileptic treatment is Timonil 750 mg/day
with a very good outcome.
Conclusions. MS is a risk factor for developing epilepsy. Patients with MS have a threefold
increase in risk for developing epilepsy when compared with that expected in the general
population. The reason for this increased risk is unclear and needs further investigation. |
URI: | https://medespera.asr.md/wp-content/uploads/ABSTRACT-BOOK.pdf http://repository.usmf.md/handle/20.500.12710/12076 |
Appears in Collections: | MedEspera 2020
|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
|