儿童期SLE病例报告

A. Alhusain, Hasan Alhashim, Wafa Almuraidif, M. Alghazal
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摘要

系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,可影响任何器官,并可能导致严重的发病率和死亡率。儿童期发作的c-SLE是一种罕见疾病,发病率为0.3-0.9/10000儿童年,患病率为3.3-8.8/100000儿童。1亚洲人、非裔美国人、西班牙裔和美洲原住民的发病率较高。2,3与成人SLE类似,c-SLE主要影响女性,约80%的受影响儿童。根据文献,中位发病年龄为11-12岁,在5岁以下的儿童中很少见。c-SLE的表现多种多样,与成人SLE相比,大多数时候是非典型的,这使得cSLE的诊断对治疗医生来说是一个挑战。4本报告显示了最终被诊断为SLE的儿科患者的一系列表现。
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Childhood onset SLE- case report
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that can affect any organ and may result in significant morbidity and mortality. Childhood-onset c-SLE is a rare disease with an incidence of 0.3-0.9/100,000 children-years and a prevalence of 3.3-8.8/100,000 children.1 Asians, African American, Hispanic and Native Americans have higher frequency of the disease.2,3 Similar to adult SLE, c-SLE affects mainly females with around 80% of the affected children. According to the literature, the median age of onset is 11-12 years and it is rare in children under 5 years of age. The manifestations of c-SLE are variable and most of the times are atypical compared to adult SLE which make the diagnosis of cSLE a challenge to the treating physician.4 This report shows a series of presentation in pediatric patient who finally was diagnosed with SLE.
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