Netherton syndrome: Temporary response to dupilumab

被引:30
|
作者
Aktas, Meryem [1 ]
Salman, Andac [1 ]
Apti Sengun, Ozlem [1 ]
Comert Ozer, Elif [1 ]
Hosgoren Tekin, Selcen [1 ]
Akin Cakici, Ozlem [1 ]
Demir, Gizem [1 ]
Ergun, Tulin [1 ]
机构
[1] Marmara Univ, Sch Med, Dept Dermatol, Istanbul, Turkey
关键词
atopic eczema; genetic diseases; mechanisms; Ichthyosis;
D O I
10.1111/pde.14362
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Netherton syndrome (NS) is an orphan disease characterized by congenital ichthyosis, hair abnormalities, and atopy, with limited treatment options. We achieved temporary improvement only during the initial 6 weeks of treatment with dupilumab, which differs from the sustained improvement observed in 2 other recently published cases. Although the clinical presentation of atopy and increased pre-allergic cytokines in NS patients suggest that dupilumab may be beneficial, larger studies are required.
引用
收藏
页码:1210 / 1211
页数:2
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