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pubmed-article:8577568pubmed:abstractTextWe present the case of a 12-year-old boy who developed progressive limbic dysfunction associated with a posterior cord syndrome in conjunction with complex partial seizures and intrathecal synthesis of IgG. Although the cerebral CT scan appeared normal, MR imaging showed signal abnormalities in both temporal lobes. As these clinical features reminded us of the well-known paraneoplastic encephalomyelitis (PNEM) in adults, we looked for a tumour and found a pelvic neuroblastoma. The diagnosis of PNEM was supported by the discovery of the antibody anti-HU in the serum of our patient.lld:pubmed
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pubmed-article:8577568pubmed:authorpubmed-author:MeyerJ JJJlld:pubmed
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pubmed-article:8577568pubmed:volume25 Suppl 1lld:pubmed
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pubmed-article:8577568pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:8577568pubmed:year1995lld:pubmed
pubmed-article:8577568pubmed:articleTitleParaneoplastic encephalomyelitis in a child with neuroblastoma.lld:pubmed
pubmed-article:8577568pubmed:affiliationService de Radiopédiatrie, Hôpital St. Vincent de Paul, F-75674 Paris Cedex 14, France.lld:pubmed
pubmed-article:8577568pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8577568pubmed:publicationTypeCase Reportslld:pubmed
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