Juvenile systemic lupus erythematosus with unusual manifestation of lupus-associated panniculitis

被引：0
|
作者：
Hashemie, H. [1 ]
Klossowski, N. [1 ]
Oommen, P. T. [2 ]
Neubert, J. [2 ]
Homey, B. [1 ]
Hoff, N. -P. [1 ]
Reifenberger, J. [1 ]
Meller, S. [1 ]
机构：
[1] Univ Klinikum Dusseldorf, Hautklin, D-40225 Dusseldorf, Germany
[2] Univ Klinikum Dusseldorf, Klin Kinder Onkol, Hamatol & Klin Immunol, D-40225 Dusseldorf, Germany
来源：
HAUTARZT | 2015年 / 66卷 / 10期
关键词：
Autoimmune diseases; ACR criteria; Combination therapy; Prednisolone; Hydroxychloroquine; ONSET;
D O I：
10.1007/s00105-015-3677-y
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
Juvenile systemic lupus erythematosus (JSLE) is a rare multisystem autoimmune disease with broad heterogeneity of clinical manifestations. Diagnosing JSLE is often very challenging. This life-threatening, unpredictable, and relapsing disease, which may affect various organ systems, requires interdisciplinary, lifelong care. Here, we report the case of a 13-year-old patient with JSLE suffering from recurrent arthralgia, lupus panniculitis, and rashes that were successfully treated with hydroxychloroquine and prednisolone.
引用
收藏
页码：718 / 720
页数：3
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