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利妥昔单抗治疗儿童发病的红斑狼疮脂膜炎。

Treatment of Childhood-Onset Lupus Erythematosus Panniculitis With Rituximab.

机构信息

Division of Rheumatology, Department of Pediatrics, University of Minnesota Masonic Children's Hospital, Minneapolis.

Division of Dermatopathology, Department of Dermatology, University of Minnesota Medical Center, Minneapolis.

出版信息

JAMA Dermatol. 2020 May 1;156(5):566-569. doi: 10.1001/jamadermatol.2019.4984.

Abstract

IMPORTANCE

Childhood-onset lupus erythematosus panniculitis (LEP) is a rare and chronic disfiguring disease. A paucity of literature exists on the clinical manifestations of this disease and how best to treat it.

OBJECTIVES

To describe the clinical features of childhood-onset LEP and report on the use of rituximab in treatment-refractory childhood-onset LEP.

DESIGN, SETTING, AND PARTICIPANTS: A retrospective, observational case series study was conducted of 4 patients with childhood-onset LEP who presented to a single-center, tertiary care clinic with pediatric dermatology and pediatric rheumatology clinics between July 1, 2014, and July 1, 2018, and were treated with rituximab. A literature review was conducted of the clinical features and treatment of childhood-onset LEP.

EXPOSURE

Rituximab therapy for childhood-onset LEP.

MAIN OUTCOMES AND MEASURES

Reduction in the number and size of erythematous and tender subcutaneous nodules (both visually and by palpation), reduction of facial atrophy (documented with serial photography), and tolerability of rituximab at 2 to 22 months after initiation of therapy.

RESULTS

Four patients (3 male; mean [SD] age at treatment, 15 [5.9] years) with refractory childhood-onset LEP were successfully treated with rituximab. All patients had a rapid and sustained response to therapy with rituximab. One patient (25%) had minor infusion reactions; otherwise, treatment was well tolerated.

CONCLUSIONS AND RELEVANCE

This case series suggests that rituximab may hold promise as a treatment for refractory, childhood-onset LEP. Larger, prospective studies are needed to validate these findings; however, given the rarity of disease, large studies may be difficult to conduct.

摘要

重要性

儿童发病的红斑狼疮脂膜炎(LEP)是一种罕见且慢性毁容性疾病。关于这种疾病的临床表现以及最佳治疗方法的文献很少。

目的

描述儿童发病的 LEP 的临床特征,并报告利妥昔单抗在治疗抵抗性儿童发病的 LEP 中的应用。

设计、设置和参与者:对 2014 年 7 月 1 日至 2018 年 7 月 1 日在一家单中心三级保健诊所就诊的 4 例儿童发病的 LEP 患者进行回顾性、观察性病例系列研究,这些患者具有儿科皮肤科和儿科风湿病学诊所,并接受利妥昔单抗治疗。对儿童发病的 LEP 的临床特征和治疗进行了文献复习。

暴露

利妥昔单抗治疗儿童发病的 LEP。

主要结果和措施

减少红斑和触痛性皮下结节的数量和大小(通过视觉和触诊)、减少面部萎缩(通过连续摄影记录),以及在开始治疗后 2 至 22 个月时利妥昔单抗的耐受性。

结果

4 例(3 例男性;治疗时的平均[SD]年龄,15[5.9]岁)难治性儿童发病的 LEP 患者成功接受利妥昔单抗治疗。所有患者对利妥昔单抗治疗均有快速和持续的反应。1 例患者(25%)出现轻微的输注反应;否则,治疗耐受性良好。

结论和相关性

本病例系列研究表明,利妥昔单抗可能是治疗难治性儿童发病的 LEP 的一种有前途的方法。需要更大的、前瞻性研究来验证这些发现;然而,由于疾病的罕见性,可能难以进行大型研究。

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