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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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