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儿童滑膜炎、痤疮、脓疱病、骨肥厚和骨炎(SAPHO)综合征的临床特征:来自单一中心的首个中国病例系列。

Clinical characteristics of pediatric synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome: the first Chinese case series from a single center.

作者信息

Wu Nan, Shao Yuming, Huo Jianwei, Zhang Yanan, Cao Yihan, Jing Hongli, Zhang Fa, Yu Chenyang, Yu Yanying, Li Chen, Song Hongmei, Zhang Wen

机构信息

Department of Orthopedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

Department of genetic research, Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing, China.

出版信息

Clin Rheumatol. 2021 Apr;40(4):1487-1495. doi: 10.1007/s10067-020-05393-w. Epub 2020 Sep 15.

Abstract

INTRODUCTION

Pediatric SAPHO syndrome is regarded as the equivalent of chronic recurrent multifocal osteomyelitis or chronic non-bacterial osteomyelitis. This study aimed to evaluate the clinical features and treatment options for Chinese pediatric patients with SAPHO syndrome.

METHOD

We conducted a single-center, retrospective study on a sample of 24 pediatric patients with SAPHO syndrome who were diagnosed at Peking Union Medical College Hospital from April 2014 to August 2018. The demographic, clinical, laboratory, imaging, histological, and therapeutic data were collected and analyzed.

RESULTS

A total of 15 boys and 9 girls were included. The mean age of onset of bone and skin symptoms was 11.7 ± 3.8 and 14.4 ± 2.7 years, respectively. The mean follow-up period was 39.2 months. Seventeen patients had skin manifestations (46% had severe acne, 100% were boys; 21% had palmoplantar pustulosis, 100% were girls). Bone lesions were localized in four of the following major regions: anterior chest wall (42%), mandible (29%), peripheral bones (50%), and spine and sacroiliac joints (21%). Six patients had been treated with non-steroidal anti-inflammatory drugs, 10 with bisphosphonate, 10 with a tumor necrosis factor-α antagonist, and 1 with glucocorticoids, with variable responses. A total of 70% of the patients had complete remission after bisphosphonate or TNF-α antagonist therapy.

CONCLUSION

Pediatric patients with SAPHO syndrome have different characteristics from other cohorts in the sex ratio, frequency of mandibular involvement, and sex distribution of skin lesions. Bisphosphonate and TNF-α antagonists show a favorable response in pediatric SAPHO syndrome treatment. Key points •Being the first study that describes an Asian pediatric SAPHO case series. •Chinese pediatric patients with SAPHO syndrome have different characteristics from Chinese adult patients and Caucasian pediatric patients.

摘要

引言

儿童SAPHO综合征被认为等同于慢性复发性多灶性骨髓炎或慢性非细菌性骨髓炎。本研究旨在评估中国儿童SAPHO综合征患者的临床特征及治疗方案。

方法

我们对2014年4月至2018年8月在北京协和医院确诊的24例儿童SAPHO综合征患者进行了单中心回顾性研究。收集并分析了人口统计学、临床、实验室、影像学、组织学及治疗数据。

结果

共纳入15例男孩和9例女孩。骨骼和皮肤症状的平均发病年龄分别为11.7±3.8岁和14.4±2.7岁。平均随访期为39.2个月。17例患者有皮肤表现(46%有重度痤疮,均为男孩;21%有掌跖脓疱病,均为女孩)。骨病变局限于以下四个主要区域之一:前胸壁(42%)、下颌骨(29%)、外周骨(50%)以及脊柱和骶髂关节(21%)。6例患者接受了非甾体抗炎药治疗,10例接受了双膦酸盐治疗,10例接受了肿瘤坏死因子-α拮抗剂治疗,1例接受了糖皮质激素治疗,反应各不相同。双膦酸盐或肿瘤坏死因子-α拮抗剂治疗后,共有70%的患者完全缓解。

结论

儿童SAPHO综合征患者在性别比例、下颌受累频率及皮肤病变的性别分布方面与其他队列不同。双膦酸盐和肿瘤坏死因子-α拮抗剂在儿童SAPHO综合征治疗中显示出良好疗效。要点•这是第一项描述亚洲儿童SAPHO病例系列的研究。•中国儿童SAPHO综合征患者与中国成年患者及白种儿童患者具有不同特征。

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