2002
DOI: 10.1590/s0100-879x2002000700007
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Use of single photon emission computed tomography and magnetic resonance to evaluate central nervous system involvement in patients with juvenile systemic lupus erythematosus

Abstract: The objective of the present study was to identify the single photon emission computed tomography (SPECT) and magnetic resonance (MR) findings in juvenile systemic lupus erythematosus (JSLE) patients with CNS involvement and to try to correlate them with neurological clinical history data and neurological clinical examination. Nineteen patients with JSLE (16 girls and 3 boys, mean age at onset 9.2 years) were submitted to neurological examination, electroencephalography, cerebrospinal fluid analysis, SPECT and… Show more

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Cited by 8 publications
(7 citation statements)
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“…Small prospective studies and retrospective reviews of conventional structural brain imaging [computed tomography (CT) and MRI] describe prominent rates of cerebral atrophy and white matter lesions in pediatric lupus patients 13,14 . There have been no published pediatric lupus MRI studies utilizing quantitative volumetric analyses.…”
Section: Rheumatologymentioning
confidence: 99%
“…Small prospective studies and retrospective reviews of conventional structural brain imaging [computed tomography (CT) and MRI] describe prominent rates of cerebral atrophy and white matter lesions in pediatric lupus patients 13,14 . There have been no published pediatric lupus MRI studies utilizing quantitative volumetric analyses.…”
Section: Rheumatologymentioning
confidence: 99%
“…Standard clinical magnetic resonance imaging (MRI) techniques using measures of ventricular size, the number of T2 hyperintense lesions, or global measures of tissue integrity () have shown a relationship to neurocognitive deficit in adults with SLE. Studies of childhood‐onset SLE suggest imaging abnormalities in 20–46% of patients, as determined using qualitative or subjective measures of lesion burden and measures of global atrophy (). However, such measures may lead to bias due to the subjective and operator‐dependent nature of the assessments, and are unable to localize specific regional involvement in childhood‐onset SLE–associated neurocognitive deficit.…”
mentioning
confidence: 99%
“…Как и в случае развития неврологических или психических нарушений у взрослых, ни один клинический, лабораторный, нейропсихологический или визуальный тест не может использоваться у детей для дифференциации нейролюпуса от других причин нейропсихиатрической симптоматики. Были проведены небольшие когортные исследования, направленные на выявление специфических биомаркеров или на оценку данных нейровизуализирующих методов исследования для уточнения особенностей нейропсихиатрических проявлений в рамках СКВ у детей, но их сложно экстраполировать на всех пациентов, а большие контролируемые исследования в этой сфере, к сожалению, не проводились [108][109][110][111][112][113][114][115][116][117][118][119][120], в связи с чем в контексте предполагаемого диагноза нейролюпуса или ухудшения неврологической и психической симптоматики исходный дифференциально-диагностический поиск должен включать все другие потенциальные причины.…”
Section: рекомендация 2 у детей и подростков с скв с новыми или необunclassified