A case of MOG encephalomyelitis with T- cell lymphoma

被引:5
作者
Kwon, Young Nam [1 ,2 ,3 ]
Koh, Jiwon [4 ]
Jeon, Yoon Kyung [4 ]
Sung, Jung-Joon [1 ,5 ]
Park, Sung-Hye [4 ]
Kim, Sung-Min [1 ,5 ]
机构
[1] Seoul Natl Univ Hosp, Dept Neurol, Seoul, South Korea
[2] Catholic Univ Korea, Eunpyeong St Marys Hosp, Dept Neurol, Seoul, South Korea
[3] Kyung Hee Univ, Dept Med, Grad Sch, Seoul, South Korea
[4] Seoul Natl Univ, Seoul Natl Univ Hosp, Dept Pathol, Coll Med, Seoul, South Korea
[5] Seoul Natl Univ, Dept Neurol, Coll Med, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Cancer; Concomitant; Malignancy; MOG; Myelin oligodendrocyte glycoprotein; encephalomyelitis;
D O I
10.1016/j.msard.2020.102038
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Myelin oligodendrocyte glycoprotein immunoglobulin-G (IgG)-associated encephalomyelitis (MOG-EM) is a distinct inflammatory demyelinating disease. We present an unusual MOG-EM cases with con- comitant T -cell lymphoma. Case report: A 38 -year -old Caucasian male presented with bilateral optic neuritis and multifocal transverse myelitis. He tested positive for MOG-IgG1 and his neurologic symptoms improved with high dose steroid treatment. Six months after his first MOG-EM symptoms, he developed ulcerative skin lesions on his leg and was diagnosed with primary cutaneous gamma delta T -cell lymphoma. The immunohistochemistry study, performed on his cancer tissue, was negative for MOG. Conclusion: Diagnosis of MOG-EM can be considered in patients with concomitant hematologic malignancy, which might be associated with the dysregulated adaptive immunity rather than the direct presentation of the onconeural antigen by cancer. Further studies need to be conducted for the risks and incidence of malignancy in a larger cohort of MOG-EM.
引用
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页数:3
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