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1.
Eur J Paediatr Neurol ; 50: 51-56, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38636242

RESUMO

BACKGROUND: Multiple sclerosis (MS) is a chronic inflammatory and demyelinating disease of the CNS. An intrathecal IgM synthesis is associated with a more rapid progression of MS and the intrathecal immune response to measles -, rubella -and varicella zoster virus (MRZR) which, if present, increases the likelihood of a diagnosis of MS in adults. OBJECTIVE: To evaluate the frequency of an intrathecal IgM synthesis and MRZR in children with MS. MethodsChildren with MS and a data set including clinical and treatment history, MRI at onset, in addition to a CSF analysis, and determination of antibody index (AI) of measles, rubella, and zoster antibodies, were eligible. The presence of an intrathecal IgM synthesis and/or a positive MRZ reaction were compared to biomarkers of a more progressive disease course. RESULTS: In 75 children with MS, OCBs were present in 93.3 %). 49,2 % experienced their first relapse within 6 months. 50.7 % had a total lesion load of more than 10 lesions in the first brain MRI. Spinal lesions were identified in 64 %. 23.5 % had a positive MRZR and 40.3 % an intrathecal IgM synthesis. No significant associations were detected between the presence of an intrathecal IgM synthesis and MRZR and parameters including the relapse rate in the first two years. CONCLUSION: An intrathecal IgM synthesis and a positive MRZR are found in a subset of MS children but are not associated with markers associated with a poor prognosis.


Assuntos
Imunoglobulina M , Imageamento por Ressonância Magnética , Esclerose Múltipla , Humanos , Masculino , Imunoglobulina M/líquido cefalorraquidiano , Criança , Feminino , Esclerose Múltipla/diagnóstico por imagem , Esclerose Múltipla/imunologia , Esclerose Múltipla/líquido cefalorraquidiano , Adolescente , Herpesvirus Humano 3/imunologia , Anticorpos Antivirais/líquido cefalorraquidiano , Anticorpos Antivirais/sangue , Pré-Escolar , Vírus do Sarampo/imunologia , Vírus da Rubéola/imunologia , Progressão da Doença , Encéfalo/diagnóstico por imagem , Biomarcadores/líquido cefalorraquidiano
2.
Eur J Paediatr Neurol ; 47: 118-130, 2023 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-38284996

RESUMO

BACKGROUND: Acute cerebellitis (AC) in children and adolescents is an inflammatory disease of the cerebellum due to viral or bacterial infections but also autoimmune-mediated processes. OBJECTIVE: To investigate the frequency of autoantibodies in serum and CSF as well as the neuroradiological features in children with AC. MATERIAL AND METHODS: Children presenting with symptoms suggestive of AC defined as acute/subacute onset of cerebellar symptoms and MRI evidence of cerebellar inflammation or additional CSF pleocytosis, positive oligoclonal bands (OCBs), and/or presence of autoantibodies in case of negative cerebellar MRI. Children fulfilling the above-mentioned criteria and a complete data set including clinical presentation, CSF studies, testing for neuronal/cerebellar and MOG antibodies as well as MRI scans performed at disease onset were eligible for this retrospective multicenter study. RESULTS: 36 patients fulfilled the inclusion criteria for AC (f:m = 14:22, median age 5.5 years). Ataxia was the most common cerebellar symptom present in 30/36 (83 %) in addition to dysmetria (15/36) or dysarthria (13/36). A substantial number of children (21/36) also had signs of encephalitis such as somnolence or seizures. In 10/36 (28 %) children the following autoantibodies (abs) were found: MOG-abs (n = 5) in serum, GFAPα-abs (n = 1) in CSF, GlyR-abs (n = 1) in CSF, mGluR1-abs (n = 1) in CSF and serum. In two further children, antibodies were detected only in serum (GlyR-abs, n = 1; GFAPα-abs, n = 1). MRI signal alterations in cerebellum were found in 30/36 children (83 %). Additional supra- and/or infratentorial lesions were present in 12/36 children, including all five children with MOG-abs. Outcome after a median follow-up of 3 months (range: 1 a 75) was favorable with an mRS ≤2 in 24/36 (67 %) after therapy. Antibody (ab)-positive children were significantly more likely to have a better outcome than ab-negative children (p = .022). CONCLUSION: In nearly 30 % of children in our study with AC, a range of abs was found, underscoring that autoantibody testing in serum and CSF should be included in the work-up of a child with suspected AC. The detection of MOG-abs in AC does expand the MOGAD spectrum.


Assuntos
Autoanticorpos , Encefalite , Adolescente , Criança , Pré-Escolar , Humanos , Ataxia , Cerebelo/diagnóstico por imagem , Encefalite/diagnóstico por imagem , Inflamação , Estudos Retrospectivos
4.
Artigo em Inglês | IMSEAR | ID: sea-31669

RESUMO

The aim of the present study was to determine the Trichinella seroprevalence in slaughter pigs in Kathmandu Valley, Nepal. Serum samples were obtained from 400 pigs at 4 major slaughterhouses and tested for Trichinella antibodies by ELISA using larval excretory-secretory (E/S) antigen. Four were positive and one was equivocal, giving a Trichinella seroprevalence of 1% (95% CI: 0.27 - 2.54). On titration, all positive and equivocal samples had titers greater than 1:80. Upon re-examination the equivocal sample failed to give a positive ELISA result. The pigs were from four major areas of Nepal, Kathmandu Valley, eastern Nepal, Terai and adjoining areas of the valley. Positive results were found from only Kathmandu Valley and adjoining areas. There was no significant difference in the prevalence between areas (p = 0.43). All four positive samples were from indoor managed pigs. The Trichinella seroprevalence determined in this study deserves a direct demonstration of the parasites for proof of the presence of Trichinella in Nepal and to discover the species and infection sources.


Assuntos
Criação de Animais Domésticos , Animais , Anticorpos Anti-Helmínticos/sangue , Estudos Transversais , Ensaio de Imunoadsorção Enzimática , Nepal/epidemiologia , Estudos Soroepidemiológicos , Suínos/sangue , Trichinella/isolamento & purificação , Triquinelose/diagnóstico
5.
Quintessence. Edición en Español;7(2): 100-104,
em Espanhol | URUGUAIODONTO | ID: odn-11207
6.
Quintessence. Edición en Español;20(1): 1-12,
em Espanhol | URUGUAIODONTO | ID: odn-20098
7.
Quintessence. Edición en Español;10(10): 653-659,
em Espanhol | URUGUAIODONTO | ID: odn-12763
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