Mario B. Prado Jr, Maria Franchesca Quinio, Karen Joy B. Adiao
{"title":"一例患有胸腺瘤相关重症肌无力的成年男性二十甲营养不良和斑秃:一例报告","authors":"Mario B. Prado Jr, Maria Franchesca Quinio, Karen Joy B. Adiao","doi":"10.1111/cen3.12761","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>To date, there is no journal that reports the coexistence of thymoma-associated myasthenia gravis, alopecia areata, and twenty-nail dystrophy. This paper hypothesizes that the presence of thymoma increases the risk of these conditions.</p>\n </section>\n \n <section>\n \n <h3> Case presentation</h3>\n \n <p>The patient was a 37-year-old Filipino who came in for a year of history of fluctuating, but progressive, left-sided ptosis and diplopia; difficulty swallowing; dysarthria; and aspiration and symmetric proximal muscle weakness confirmed to be myasthenia gravis by abnormal repetitive nerve stimulation and the presence of thymoma on histology. Before his thymectomy, he also developed gradually worsening thinning and longitudinal ridging of all fingernails and toenails; and patches of bald areas on the scalp; diagnosed to be twenty-nail dystrophy and alopecia areata, respectively, by a board-certified dermatologist.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Thymoma is the possible risk factor and link for the co-occurrence of the three conditions in the present patient.</p>\n </section>\n </div>","PeriodicalId":10193,"journal":{"name":"Clinical and Experimental Neuroimmunology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Twenty-nail dystrophy and alopecia areata in an adult male with thymoma-associated myasthenia gravis: A case report\",\"authors\":\"Mario B. Prado Jr, Maria Franchesca Quinio, Karen Joy B. Adiao\",\"doi\":\"10.1111/cen3.12761\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>To date, there is no journal that reports the coexistence of thymoma-associated myasthenia gravis, alopecia areata, and twenty-nail dystrophy. This paper hypothesizes that the presence of thymoma increases the risk of these conditions.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Case presentation</h3>\\n \\n <p>The patient was a 37-year-old Filipino who came in for a year of history of fluctuating, but progressive, left-sided ptosis and diplopia; difficulty swallowing; dysarthria; and aspiration and symmetric proximal muscle weakness confirmed to be myasthenia gravis by abnormal repetitive nerve stimulation and the presence of thymoma on histology. Before his thymectomy, he also developed gradually worsening thinning and longitudinal ridging of all fingernails and toenails; and patches of bald areas on the scalp; diagnosed to be twenty-nail dystrophy and alopecia areata, respectively, by a board-certified dermatologist.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>Thymoma is the possible risk factor and link for the co-occurrence of the three conditions in the present patient.</p>\\n </section>\\n </div>\",\"PeriodicalId\":10193,\"journal\":{\"name\":\"Clinical and Experimental Neuroimmunology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-06-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical and Experimental Neuroimmunology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/cen3.12761\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Immunology and Microbiology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and Experimental Neuroimmunology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/cen3.12761","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
Twenty-nail dystrophy and alopecia areata in an adult male with thymoma-associated myasthenia gravis: A case report
Background
To date, there is no journal that reports the coexistence of thymoma-associated myasthenia gravis, alopecia areata, and twenty-nail dystrophy. This paper hypothesizes that the presence of thymoma increases the risk of these conditions.
Case presentation
The patient was a 37-year-old Filipino who came in for a year of history of fluctuating, but progressive, left-sided ptosis and diplopia; difficulty swallowing; dysarthria; and aspiration and symmetric proximal muscle weakness confirmed to be myasthenia gravis by abnormal repetitive nerve stimulation and the presence of thymoma on histology. Before his thymectomy, he also developed gradually worsening thinning and longitudinal ridging of all fingernails and toenails; and patches of bald areas on the scalp; diagnosed to be twenty-nail dystrophy and alopecia areata, respectively, by a board-certified dermatologist.
Conclusion
Thymoma is the possible risk factor and link for the co-occurrence of the three conditions in the present patient.