{"title":"重症肌无力和胸腺瘤相关的自身免疫性神经节性肠病","authors":"G. Kanabar, D. Kidd","doi":"10.47496/nl.acr.2020.01.02","DOIUrl":null,"url":null,"abstract":"Background: Autonomic neuropathies causing gastrointestinal complications are uncommon. Case \nPresentation: We report a case in which autoimmune autonomic enteric neuropathy was associated with \nmyasthenia gravis and thymoma. Conclusion: Autoimmune autonomic enteric neuropathies are \nexceedingly rare, with only 10 cases reported in the literature to date. All have been associated with \nthymoma. We describe the prevalence of associated antibodies, summarise the previous cases and treatment \nreceived.","PeriodicalId":7334,"journal":{"name":"Advances in Computing Research","volume":"60 1","pages":"1-3"},"PeriodicalIF":0.0000,"publicationDate":"2020-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Autoimmune Ganglionic Enteropathy Associated with Myasthenia Gravis and Thymoma\",\"authors\":\"G. Kanabar, D. Kidd\",\"doi\":\"10.47496/nl.acr.2020.01.02\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Autonomic neuropathies causing gastrointestinal complications are uncommon. Case \\nPresentation: We report a case in which autoimmune autonomic enteric neuropathy was associated with \\nmyasthenia gravis and thymoma. Conclusion: Autoimmune autonomic enteric neuropathies are \\nexceedingly rare, with only 10 cases reported in the literature to date. All have been associated with \\nthymoma. We describe the prevalence of associated antibodies, summarise the previous cases and treatment \\nreceived.\",\"PeriodicalId\":7334,\"journal\":{\"name\":\"Advances in Computing Research\",\"volume\":\"60 1\",\"pages\":\"1-3\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-09-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advances in Computing Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.47496/nl.acr.2020.01.02\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Computing Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47496/nl.acr.2020.01.02","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Autoimmune Ganglionic Enteropathy Associated with Myasthenia Gravis and Thymoma
Background: Autonomic neuropathies causing gastrointestinal complications are uncommon. Case
Presentation: We report a case in which autoimmune autonomic enteric neuropathy was associated with
myasthenia gravis and thymoma. Conclusion: Autoimmune autonomic enteric neuropathies are
exceedingly rare, with only 10 cases reported in the literature to date. All have been associated with
thymoma. We describe the prevalence of associated antibodies, summarise the previous cases and treatment
received.