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EEG in Sarcoidosis Patients Without Neurological Findings.

Authors :
Bilgin Topçuoğlu Ö
Kavas M
Öztaş S
Arınç S
Afşar G
Saraç S
Midi İ
Source :
Clinical EEG and neuroscience [Clin EEG Neurosci] 2017 Jan; Vol. 48 (1), pp. 54-59. Date of Electronic Publication: 2016 Apr 22.
Publication Year :
2017

Abstract

Sarcoidosis is a multisystem granulomatous disease affecting nervous system in 5% to 10% of patients. Magnetic resonance imaging (MRI) is accepted as the most sensitive method for detecting neurosarcoidosis. However, the most common findings in MRI are the nonspecific white matter lesions, which may be unrelated to sarcoidosis and can occur because of hypertension, diabetes mellitus, smoking, and other inflammatory or infectious disorders, as well. Autopsy studies report more frequent neurological involvement than the ante mortem studies. The aim of this study is to assess electroencephalography (EEG) in sarcoidosis patients without neurological findings in order to display asymptomatic neurological dysfunction. We performed EEG on 30 sarcoidosis patients without diagnosis of neurosarcoidosis or prior neurological comorbidities. Fourteen patients (46.7%) showed intermittant focal and/or generalized slowings while awake and not mentally activated. Seven (50%) of these 14 patients with EEG slowings had nonspecific white matter changes while the other half showed EEG slowings in the absence of MRI changes. We conclude that EEG slowings, when normal variants (psychomotor variant, temporal theta of elderly, frontal theta waves) are eliminated, may be an indicator of dysfunction in brain activity even in the absence of MRI findings. Hence, EEG may contribute toward detecting asymptomatic neurological dysfunction or probable future neurological involvement in sarcoidosis patients.<br /> (© EEG and Clinical Neuroscience Society (ECNS) 2016.)

Details

Language :
English
ISSN :
2169-5202
Volume :
48
Issue :
1
Database :
MEDLINE
Journal :
Clinical EEG and neuroscience
Publication Type :
Academic Journal
Accession number :
27107024
Full Text :
https://doi.org/10.1177/1550059416646651