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

页码：718 / 720

页数：3

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