| Literature DB >> 1379422 |
A B Younes-Chennoufi1, J M Léger, J J Hauw, J L Preud'homme, P Bouche, P Aucouturier, H Ratinahirana, C Lubetzki, O Lyon-Caen, N Baumann.
Abstract
We report on a 54-year-old man with a sensory-motor polyneuropathy associated with a biclonal IgM-kappa gammopathy, which reacted with the ganglioside GD1b. Examination of nerve biopsy specimens showed some reduction in the density of myelinated fibers and axonal degeneration with a loss of large fibers and a relative increase in the density of small fibers. Immunodetection on thin-layer chromatography of the glycolipid antigens showed strong reactivity of the patient's serum IgM-kappa with GD1b ganglioside and weak binding to GD1a. biclonal IgM antibodies did not react with GM1, asialo-GM1, GT1b, GD2, or GD3. Indirect immunofluorescence staining showed binding of IgM-kappa mainly in a crescent-like pattern on the internal side of myelin sheaths, which could correspond either to an enlarged periaxonal (adaxonal) space or to the internal mesaxon or to both. The immunostaining was abolished after absorption of the serum with GD1b.Entities:
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Year: 1992 PMID: 1379422 DOI: 10.1002/ana.410320105
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422