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

Q4 Immunology and Microbiology Clinical and Experimental Neuroimmunology Pub Date : 2023-06-20 DOI:10.1111/cen3.12761
Mario B. Prado Jr, Maria Franchesca Quinio, Karen Joy B. Adiao
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引用次数: 0

摘要

到目前为止,没有任何期刊报道胸腺瘤相关重症肌无力、斑秃和二十甲营养不良的共存。本文假设胸腺瘤的存在会增加这些情况的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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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.

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来源期刊
Clinical and Experimental Neuroimmunology
Clinical and Experimental Neuroimmunology Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
1.60
自引率
0.00%
发文量
52
期刊最新文献
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