Mycophenolate mofetil after tacrolimus for refractory clinically amyopathic dermatomyositis: a case report

被引:0
|
作者
Ling, Gui-Chen [1 ]
Su, Chang [1 ,2 ]
Guo, Ying-Ao [1 ]
Qiu, Xia [1 ,2 ]
Liu, Jia-Wei [3 ]
Xiao, Min [1 ,2 ]
Xiao, Yu-Ya [1 ,2 ]
Yang, Shuo [1 ]
Zhang, Jian-Yong [1 ,2 ]
Xie, Jing-Jing [1 ,2 ]
机构
[1] Guangzhou Univ Chinese Med, Clin Med Coll 4, Shenzhen, Guangdong, Peoples R China
[2] Shenzhen Tradit Chinese Med Hosp, Dept Rheumatol, Shenzhen, Guangdong, Peoples R China
[3] Univ Hong Kong, Shenzhen Hosp, Dept Tradit Chinese Med, Shenzhen, Guangdong, Peoples R China
关键词
anti-MDA5-associated dermatomyositis; case report; rapidly progressive interstitial lung disease; mycophenolate mofetil; clinically amyopathic dermatomyositis (CADM); INTERSTITIAL LUNG-DISEASE; COMPLICATION; IL-8;
D O I
10.3389/fphar.2024.1472667
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dermatomyositis (DM) positive for anti-melanoma differentiation-associated gene 5 (MDA5) antibodies, mainly when linked with rapidly progressive interstitial lung disease (RP-ILD), is considered a refractory disease. Our report describes a critical case of clinically amyopathic dermatomyositis (CADM) with RP-ILD that tested positive for both anti-MDA5 and anti-Ro-52 antibodies. The patient showed a limited response to a combined therapy regimen of prednisone, iguratimod, and tacrolimus. However, after adjunct therapy with mycophenolate mofetil (MMF), the patient's condition was controlled, his serum KL-6 levels decreased, and anti-MDA5 antibodies became negative. During the 68-week follow-up, the patient's condition remained stable, with a satisfactory quality of life. This report also discusses the potential role of inflammatory cytokines in the pathophysiology of CADM and RP-ILD. Further research is required to confirm these results and investigate the application of MMF in maintenance therapy for CADM-associated RP-ILD.
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页数:7
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