Successful peficitinib addition on anti-MDA5 antibody-positive dermatomyositis refractory to triple therapy and glucocorticoid reduction

被引:4
作者
Oba, Yuki [1 ,2 ]
Yamanouchi, Masayuki
Ikuma, Daisuke
Mizuno, Hiroki
Inoue, Noriko
Sekine, Akinari
Hasegawa, Eiko
Suwabe, Tatsuya
Sawa, Naoki
Ubara, Yoshifumi
机构
[1] Toranomon Hosp Kajigaya, Nephrol Ctr, 1-3-1 Takatsu, Kawasaki, Kanagawa 2120015, Japan
[2] Toranomon Hosp Kajigaya, Dept Rheumatol, 1-3-1 Takatsu, Kawasaki, Kanagawa 2120015, Japan
来源
SAGE OPEN MEDICAL CASE REPORTS | 2022年 / 10卷
关键词
Anti-MDA5 antibody-positive dermatomyositis; interstitial lung disease; triple therapy; JAK inhibitor; peficitinib; INTERSTITIAL LUNG-DISEASE; GENE; 5;
D O I
10.1177/2050313X221141277
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anti-melanoma differentiation-associated gene 5 antibody-positive dermatomyositis is the poorest prognosis of all dermatomyositis due to its associated rapidly progressive interstitial lung disease. Intensive treatment is required from the onset and triple therapy with prednisolone, calcineurin inhibitors, and intravenous cyclophosphamide is recommended. However, some patients are refractory or dependent on this treatment and additional immunosuppressive therapy is required. Recently, the efficacy of tofacitinib, a JAK inhibitor, has been reported. Here, we describe a case of a 50-year-old woman with anti-melanoma differentiation-associated gene 5 antibody-positive dermatomyositis who became refractory to triple therapy and prednisolone reduction, and achieved remission with the addition of peficitinib, a JAK inhibitor. This is the first report showing that peficitinib is effective for anti-melanoma differentiation-associated gene 5 antibody-positive dermatomyositis and it may be a potential treatment option.
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页数:6
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