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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.

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。

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