| Literature DB >> 12504207 |
Michael R Pranzatelli1, Elizabeth D Tate, Alisa Wheeler, Nancy Bass, Arnold P Gold, May L Griebel, Maria Gumbinas, Peter T Heydemann, Philip J Holt, Pierre Jacob, Suresh Kotagal, Chester J Minarcik, Howard S Schub.
Abstract
Various paraneoplastic autoantibodies have been linked to discrete neurologic syndromes and tumors in adults, but little is known about their incidence in children. We report a cross-sectional study of known paraneoplastic antibodies in 59 children with opsoclonus-myoclonus-ataxia, 86% of whom were moderately or severely symptomatic, and 68% of whom had relapsed at the time of testing. This total number of patients includes 18 children with low-stage neuroblastoma (tested after tumor resection), six of whom had never been treated with immunosuppressants. All were seronegative for anti-Hu, anti-Ri, and anti-Yo, the three paraneoplastic antibodies most associated with opsoclonus-myoclonus or ataxia in adults. These data contrast with reports of anti-Hu-positive sera in children with high-stage tumors and suggest that anti-Hu, anti-Ri, and anti-Yo do not explain relapses in pediatric opsoclonus-myoclonus-ataxia. They underscore the need to search for unique autoantibodies, as well as cellular mechanisms of pediatric paraneoplastic disease.Entities:
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Year: 2002 PMID: 12504207 DOI: 10.1016/s0887-8994(02)00457-5
Source DB: PubMed Journal: Pediatr Neurol ISSN: 0887-8994 Impact factor: 3.372