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本文引用的文献

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A single-center study of clinical features of pediatric Sjögren's syndrome.一项关于儿童干燥综合征临床特征的单中心研究。
Pediatr Rheumatol Online J. 2023 Oct 13;21(1):119. doi: 10.1186/s12969-023-00902-y.
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Clinical and laboratory features of childhood-onset primary Sjögren's syndrome: A retrospective study from China.儿童期起病的原发性干燥综合征的临床和实验室特征:一项来自中国的回顾性研究。
Front Pediatr. 2023 Jan 4;10:1044812. doi: 10.3389/fped.2022.1044812. eCollection 2022.
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Not all autoantibodies are clinically relevant. Classic and novel autoantibodies in Sjögren's syndrome: A critical review.并非所有的自身抗体都具有临床意义。干燥综合征中的经典和新型自身抗体:批判性综述。
Front Immunol. 2022 Oct 17;13:1003054. doi: 10.3389/fimmu.2022.1003054. eCollection 2022.
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Diagnostic utility of a second minor salivary gland biopsy in patients with suspected Sjögren's syndrome: A retrospective cohort study.疑似干燥综合征患者的第二次小唾液腺活检的诊断效用:一项回顾性队列研究。
Joint Bone Spine. 2023 Jan;90(1):105459. doi: 10.1016/j.jbspin.2022.105459. Epub 2022 Sep 13.
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Differences in presentation between paediatric- and adult-onset primary Sjögren's syndrome patients.儿童期和成人期发病的原发性干燥综合征患者临床表现的差异。
Clin Exp Rheumatol. 2021 Nov-Dec;39 Suppl 133(6):85-92. doi: 10.55563/clinexprheumatol/vxe6h0. Epub 2021 Nov 10.
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Polyautoimmunity in systemic lupus erythematosus: secondary Sjogren syndrome.系统性红斑狼疮中的多器官自身免疫病:继发干燥综合征。
Z Rheumatol. 2023 Jan;82(Suppl 1):68-73. doi: 10.1007/s00393-021-01051-x. Epub 2021 Jul 21.
7
The Diagnostic Performance of Early Sjögren's Syndrome Autoantibodies in Juvenile Sjögren's Syndrome: The University of Florida Pediatric Cohort Study.早期干燥综合征自身抗体对青少年干燥综合征的诊断性能:佛罗里达大学儿科队列研究。
Front Immunol. 2021 Jun 25;12:704193. doi: 10.3389/fimmu.2021.704193. eCollection 2021.
8
Accuracy of minor salivary gland biopsy in the diagnosis of Sjögren syndrome.小唾液腺活检在干燥综合征诊断中的准确性。
Bratisl Lek Listy. 2021;122(7):454-460. doi: 10.4149/BLL_2021_075.
9
A biomarker for lymphoma development in Sjogren's syndrome: Salivary gland focus score.干燥综合征中淋巴瘤发展的生物标志物:唾液腺灶评分。
J Autoimmun. 2021 Jul;121:102648. doi: 10.1016/j.jaut.2021.102648. Epub 2021 May 21.
10
Childhood-onset of primary Sjögren's syndrome: phenotypic characterization at diagnosis of 158 children.儿童期起病的原发性干燥综合征:158例儿童诊断时的表型特征
Rheumatology (Oxford). 2021 Oct 2;60(10):4558-4567. doi: 10.1093/rheumatology/keab032.

系统性红斑狼疮合并干燥综合征患儿的临床特征及唇腺病理特点

[Clinical characteristics and labial gland pathological features in children with systemic lupus erythematosus complicated by Sjögren's syndrome].

作者信息

Cheng Sang, Xue Hai-Yan, Cao Lan-Fang

机构信息

Department of Pediatrics, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200001, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2024 Jul 15;26(7):695-700. doi: 10.7499/j.issn.1008-8830.2402073.

DOI:10.7499/j.issn.1008-8830.2402073
PMID:39014945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11562035/
Abstract

OBJECTIVES

To study the clinical manifestations, laboratory features, and labial gland pathological features in children with systemic lupus erythematosus (SLE) complicated by Sjögren's syndrome (SS).

METHODS

A retrospective analysis was conducted on 102 children with SLE who underwent labial gland biopsies at Renji Hospital, Shanghai Jiao Tong University School of Medicine from January 2013 to December 2022. The children were divided into two groups based on the presence of SS: the SLE with SS group (SLE-SS; 60 children) and the SLE-only group (42 children). According to the focus score (FS) of the labial glands, children in the SLE-SS group were further subdivided into FS≥4 subgroup (26 children) and FS<4 subgroup (34 children). The clinical data of the groups were compared.

RESULTS

Compared to the SLE-only group, children in the SLE-SS group had less skin and mucosal involvement, were more likely to have positive anti-SSA and anti-SSB antibodies, and had higher levels of rheumatoid factor (<0.05). There was no significant difference in treatment protocols between the two groups (>0.05). Compared to the FS<4 subgroup, the FS≥4 subgroup had more frequent musculoskeletal involvement (<0.05), but there was no significant difference in SLE disease activity or other major organ involvement between the subgroups (>0.05).

CONCLUSIONS

Children with SLE complicated by SS are less likely to have skin and mucous membrane involvement and exhibit specific serological characteristics. The SLE-SS children with an FS≥4 are more likely to experience musculoskeletal involvement. However, FS is not associated with disease activity or other significant organ damage.

摘要

目的

研究系统性红斑狼疮(SLE)合并干燥综合征(SS)患儿的临床表现、实验室特征及唇腺病理特征。

方法

对2013年1月至2022年12月在上海交通大学医学院附属仁济医院接受唇腺活检的102例SLE患儿进行回顾性分析。根据是否存在SS将患儿分为两组:SLE合并SS组(SLE-SS;60例患儿)和单纯SLE组(42例患儿)。根据唇腺灶性评分(FS),SLE-SS组患儿进一步分为FS≥4亚组(26例患儿)和FS<4亚组(34例患儿)。比较各组的临床资料。

结果

与单纯SLE组相比,SLE-SS组患儿皮肤和黏膜受累较少,抗SSA和抗SSB抗体阳性的可能性更大,类风湿因子水平更高(<0.05)。两组治疗方案无显著差异(>0.05)。与FS<4亚组相比,FS≥4亚组肌肉骨骼受累更频繁(<0.05),但亚组间SLE疾病活动度或其他主要器官受累情况无显著差异(>0.05)。

结论

SLE合并SS的患儿皮肤和黏膜受累的可能性较小,并表现出特定的血清学特征。FS≥4的SLE-SS患儿肌肉骨骼受累的可能性更大。然而,FS与疾病活动度或其他重要器官损害无关。