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[系统性红斑狼疮患儿的临床特征及随访结果:一项对比分析]

[Clinical features and follow-up results of boys and girls with systemic lupus erythematosus: a comparative analysis].

作者信息

Chen Wei-Na, Luo Xiu, Si You-Hua, Xu Cai-Qi, Liang Li-Jun

机构信息

Ningxia Medical University, Yinchuan, Ningxia 750004, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2020 Feb;22(2):164-170. doi: 10.7499/j.issn.1008-8830.2020.02.015.

DOI:10.7499/j.issn.1008-8830.2020.02.015
PMID:32051085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7390018/
Abstract

OBJECTIVE

To compare the clinical features and follow-up results of systemic lupus erythematosus (SLE) between boys and girls.

METHODS

A retrospective analysis was performed for the clinical data of 79 children (18 boys and 61 girls), aged ≤14 years, who were diagnosed with SLE from 2008 to 2018. The boys and the girls were compared in terms of initial and major clinical symptoms, injury of organs/systems, related laboratory markers, and follow-up results.

RESULTS

As for the initial and non-initial symptoms, fever had the highest incidence rate in the boys, while facial erythema had the highest incidence rate in the girls. The boys tended to develop renal injury and hematological damage (P<0.05), with a significantly higher incidence rate of proteinuria than the girls (P<0.05), while the girls tended to develop joint pain (P<0.05). There were high abnormal rates (>80%) of anti-nuclear antibody, dsDNA, complement C3, and erythrocyte sedimentation rate in both boys and girls (P>0.05). The boys had a significantly higher disease activity than the girls at the first visit and in year 9 of follow-up (P<0.05). A one-month to ten-year follow-up showed that among the boys, 3 were lost to follow-up, 1 died, 7 were well controlled but required oral administration of large doses of hormones or immunosuppression, 2 progressed to chronic renal failure, and 1 developed lupus encephalopathy. Among the girls, 3 were lost to follow-up; 5 died; 34 were well controlled, among whom 5 were maintained on oral prednisone acetate with a dose of <10 mg, 1 was withdrawn from the drug for 1 year, and 2 were withdrawn from the drug for 2 years; 4 developed lupus encephalopathy; 1 developed depression and anxiety and had suicidal tendency in the 7th year after disease onset; 2 experienced impaired vision, blurred vision, and chloropsia; 1 developed a vascular necrosis of both femoral heads in the 3rd year of hormone administration.

CONCLUSIONS

There are differences in clinical features, several laboratory markers, and prognosis between boys and girls with SLE. Boys tend to have a high severity at disease onset, develop renal injury and hematological damage, and have poor long-term prognosis, while girls tend to have joint involvement.

摘要

目的

比较男孩和女孩系统性红斑狼疮(SLE)的临床特征及随访结果。

方法

对2008年至2018年确诊为SLE的79例14岁及以下儿童(18例男孩和61例女孩)的临床资料进行回顾性分析。比较男孩和女孩的初始及主要临床症状、器官/系统损伤、相关实验室指标及随访结果。

结果

在初始及非初始症状方面,发热在男孩中的发生率最高,而面部红斑在女孩中的发生率最高。男孩易发生肾损伤和血液系统损害(P<0.05),蛋白尿发生率显著高于女孩(P<0.05),而女孩易发生关节疼痛(P<0.05)。男孩和女孩的抗核抗体、双链DNA、补体C3及红细胞沉降率异常率均较高(>80%)(P>0.05)。男孩在首次就诊及随访第9年时疾病活动度显著高于女孩(P<0.05)。1个月至10年的随访显示,男孩中,3例失访,1例死亡,7例病情得到良好控制但需口服大剂量激素或免疫抑制剂,2例进展为慢性肾衰竭,1例发生狼疮脑病。女孩中,3例失访;5例死亡;34例病情得到良好控制,其中5例口服醋酸泼尼松剂量<10 mg维持治疗,1例停药1年,2例停药2年;4例发生狼疮脑病;1例在发病后第7年出现抑郁、焦虑并有自杀倾向;2例出现视力减退、视物模糊及黄视;1例在使用激素第3年发生双侧股骨头血管性坏死。

结论

SLE男孩和女孩在临床特征、多项实验室指标及预后方面存在差异。男孩发病时病情往往较重,易发生肾损伤和血液系统损害且长期预后较差,而女孩易出现关节受累。

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本文引用的文献

1
Systemic lupus erythematosus: nothing stale her infinite variety.系统性红斑狼疮:她的多样性无穷无尽。
Mod Rheumatol. 2018 Sep;28(5):758-765. doi: 10.1080/14397595.2018.1494239.
2
[Imaging findings of bone infarction in children with systemic lupus erythematosus].[系统性红斑狼疮患儿骨梗死的影像学表现]
Zhongguo Gu Shang. 2018 Mar 25;31(3):272-275. doi: 10.3969/j.issn.1003-0034.2018.03.016.
3
The worldwide incidence and prevalence of systemic lupus erythematosus: a systematic review of epidemiological studies.系统性红斑狼疮的全球发病率和患病率:流行病学研究的系统评价
Rheumatology (Oxford). 2017 Nov 1;56(11):1945-1961. doi: 10.1093/rheumatology/kex260.
4
European evidence-based recommendations for the diagnosis and treatment of childhood-onset lupus nephritis: the SHARE initiative.欧洲基于证据的儿童发病狼疮肾炎诊断和治疗推荐:SHARE 倡议。
Ann Rheum Dis. 2017 Dec;76(12):1965-1973. doi: 10.1136/annrheumdis-2017-211898. Epub 2017 Sep 6.
5
Comparison of Disease Characteristics, Organ Damage, and Survival in Patients with Juvenile-onset and Adult-onset Systemic Lupus Erythematosus in a Combined Cohort from 2 Tertiary Centers in Turkey.土耳其两家三级中心联合队列中青少年起病型和成人起病型系统性红斑狼疮患者的疾病特征、器官损害及生存率比较
J Rheumatol. 2017 May;44(5):619-625. doi: 10.3899/jrheum.160340. Epub 2017 Mar 15.
6
Update on the pathogenesis and treatment of childhood-onset systemic lupus erythematosus.儿童发病系统性红斑狼疮发病机制和治疗的最新进展。
Curr Opin Rheumatol. 2016 Sep;28(5):488-96. doi: 10.1097/BOR.0000000000000317.
7
Drug-induced systemic lupus erythematosus in a child after 3 years of treatment with carbamazepine.一名儿童在接受卡马西平治疗3年后出现药物性系统性红斑狼疮。
Australas J Dermatol. 2017 Feb;58(1):e20-e22. doi: 10.1111/ajd.12393. Epub 2015 Sep 30.
8
The outcome of patients with renal involvement in pediatric-onset systemic lupus erythematosus--a 20-year experience in Asia.亚洲 20 年经验:儿童起病系统性红斑狼疮患者肾脏受累的结局。
Lupus. 2013 Dec;22(14):1534-40. doi: 10.1177/0961203313502110. Epub 2013 Aug 21.
9
Predictors of survival in systemic lupus erythematosus.系统性红斑狼疮的生存预测因素。
Medicine (Baltimore). 2006 May;85(3):147-156. doi: 10.1097/01.md.0000224709.70133.f7.
10
Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus.更新美国风湿病学会系统性红斑狼疮分类的修订标准。
Arthritis Rheum. 1997 Sep;40(9):1725. doi: 10.1002/art.1780400928.