A young female case of asymptomatic immune-mediated necrotizing myopathy: a potential diagnostic option of antibody testing for rhabdomyolysis

被引:3
|
作者
Sasaki, Ryo [1 ]
Yunoki, Taijun [1 ]
Nakano, Yumiko [1 ]
Fukui, Yusuke [1 ]
Takemoto, Mami [1 ]
Morihara, Ryuta [1 ]
Katsuyama, Eri [2 ]
Nishino, Ichizo [3 ]
Yamashita, Toru [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Neurol, 2-5-1 Shikata Cho,Kita Ku, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Nephrol Rheumatol Endocrinol & Metab, 2-5-1 Shikata Cho,Kita Ku, Okayama 7008558, Japan
[3] Natl Ctr Neurol & Psychiat NCNP, Natl Inst Neurosci, Dept Neuromuscular Res, 4-1-1 Ogawahigashi Cho, Tokyo 1878502, Japan
关键词
HMGCR; IMNM; Myopathy; Asymptomatic; MTX; IVIg; CLINICAL-FEATURES; ANTI-3-HYDROXY-3-METHYLGLUTARYL-COENZYME;
D O I
10.1016/j.nmd.2022.12.012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) immune-mediated necrotizing myopathy (IMNM) is a neuromuscular disorder that presents muscle weakness in proximal extremities and/or the trunk with an elevation of creatine kinase (CK). Young and asymptomatic anti-HMGCR IMNM patients are very rare and a treatment regimen has not been established. The present case, a 17-year-old woman without any muscular symptoms, only showed hyperCKemia that was detected by chance. After close examinations, including a muscle biopsy and antibody search, she was diagnosed as anti-HMGCR IMNM, and initial treatment with methotrexate and continuous intravenous immunoglobulin seemed to be effective. The present case is the unusually young asymptomatic case of anti-HMGCR IMNM. The diagnosis was successfully made, leading to the early introduction of a treatment. Given the course of this case, we believe that the preceding antibody testing is one of the diagnostic option for rhabdomyolysis.(c) 2022 Elsevier B.V. All rights reserved.
引用
收藏
页码:183 / 186
页数:4
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