{"title":"IgM抗神经束蛋白155联合中枢和外周脱髓鞘:1例报告。","authors":"Antoine Pegat, Emilien Delmont, Juliette Svahn, Emilien Bernard, Lola Lessard, Romain Marignier, Francoise Bouhour","doi":"10.1212/NXI.0000000000001160","DOIUrl":null,"url":null,"abstract":"Immunoglobulin (Ig) G anti – neurofascin 155 antibodies (anti-NF155 Abs) have been described in rare forms of chronic in fl ammatory demyelinating polyradiculoneuropathy (CIDP) and in combined central and peripheral demyelination (CCPD). 1 We report herein a case of a patient presenting CCPD and IgM anti-NF155 Ab. quadridistal hypesthesia, gait, tendon re fl exes. Overall Neuropathy Limitations (ONLS) was 1/12. Electroneuromyography (ENMG) revealed a di ff use homogeneous demyelinating neuropathy. Nerve ultrasonography and of the cervical plexus 1, D and a di ff use enlargement of peripheral structures. CSF analysis showed elevated protein level (0.7 g/L, normal <0.4) and 14 white blood cells/mm 3 (normal <2) with oligoclonal IgG bands. Cerebral MRI revealed multiple hyperintensities in the periventricular and juxtacortical white matter (diagnosis of radiologically isolated syn-drome). All the 97 genes of a panel of genes involved in hereditary neuropathies, especially demyelinating Charcot-Marie-Tooth (CMT), were negative. Peripheral","PeriodicalId":520720,"journal":{"name":"Neurology(R) neuroimmunology & neuroinflammation","volume":" ","pages":""},"PeriodicalIF":7.5000,"publicationDate":"2022-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/0e/e4/NEURIMMINFL2021039570.PMC8936685.pdf","citationCount":"1","resultStr":"{\"title\":\"Combined Central and Peripheral Demyelination With IgM Anti-Neurofascin 155 Antibodies: Case Report.\",\"authors\":\"Antoine Pegat, Emilien Delmont, Juliette Svahn, Emilien Bernard, Lola Lessard, Romain Marignier, Francoise Bouhour\",\"doi\":\"10.1212/NXI.0000000000001160\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Immunoglobulin (Ig) G anti – neurofascin 155 antibodies (anti-NF155 Abs) have been described in rare forms of chronic in fl ammatory demyelinating polyradiculoneuropathy (CIDP) and in combined central and peripheral demyelination (CCPD). 1 We report herein a case of a patient presenting CCPD and IgM anti-NF155 Ab. quadridistal hypesthesia, gait, tendon re fl exes. Overall Neuropathy Limitations (ONLS) was 1/12. Electroneuromyography (ENMG) revealed a di ff use homogeneous demyelinating neuropathy. Nerve ultrasonography and of the cervical plexus 1, D and a di ff use enlargement of peripheral structures. CSF analysis showed elevated protein level (0.7 g/L, normal <0.4) and 14 white blood cells/mm 3 (normal <2) with oligoclonal IgG bands. Cerebral MRI revealed multiple hyperintensities in the periventricular and juxtacortical white matter (diagnosis of radiologically isolated syn-drome). All the 97 genes of a panel of genes involved in hereditary neuropathies, especially demyelinating Charcot-Marie-Tooth (CMT), were negative. Peripheral\",\"PeriodicalId\":520720,\"journal\":{\"name\":\"Neurology(R) neuroimmunology & neuroinflammation\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":7.5000,\"publicationDate\":\"2022-03-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/0e/e4/NEURIMMINFL2021039570.PMC8936685.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurology(R) neuroimmunology & neuroinflammation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1212/NXI.0000000000001160\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/5/1 0:00:00\",\"PubModel\":\"Print\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurology(R) neuroimmunology & neuroinflammation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1212/NXI.0000000000001160","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/5/1 0:00:00","PubModel":"Print","JCR":"","JCRName":"","Score":null,"Total":0}
Combined Central and Peripheral Demyelination With IgM Anti-Neurofascin 155 Antibodies: Case Report.
Immunoglobulin (Ig) G anti – neurofascin 155 antibodies (anti-NF155 Abs) have been described in rare forms of chronic in fl ammatory demyelinating polyradiculoneuropathy (CIDP) and in combined central and peripheral demyelination (CCPD). 1 We report herein a case of a patient presenting CCPD and IgM anti-NF155 Ab. quadridistal hypesthesia, gait, tendon re fl exes. Overall Neuropathy Limitations (ONLS) was 1/12. Electroneuromyography (ENMG) revealed a di ff use homogeneous demyelinating neuropathy. Nerve ultrasonography and of the cervical plexus 1, D and a di ff use enlargement of peripheral structures. CSF analysis showed elevated protein level (0.7 g/L, normal <0.4) and 14 white blood cells/mm 3 (normal <2) with oligoclonal IgG bands. Cerebral MRI revealed multiple hyperintensities in the periventricular and juxtacortical white matter (diagnosis of radiologically isolated syn-drome). All the 97 genes of a panel of genes involved in hereditary neuropathies, especially demyelinating Charcot-Marie-Tooth (CMT), were negative. Peripheral