Coronel Luis, Gouze Hélène, Gudu Tania, Ruel-Gagné Sophie, Padovano Ilaria, Costantino Félicie, Vidal François, Breban Maxime, Mahé Emmanuel, D'Agostino Maria-Antonietta
Rheumatology Division, Hôpital Ambroise-Paré, APHP-Université Paris-Saclay, France.
Rheumatology Division, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Rheumatology (Oxford). 2024 May 2;63(5):1391-1396. doi: 10.1093/rheumatology/kead398.
To evaluate the prevalence of clinical and US (grey-scale and Doppler) abnormalities in joints, periarticular structures and nails of children affected by skin psoriasis (PsO).
We conducted a cross-sectional study including consecutive children affected by PsO. A systematic clinical and US evaluation of joints, entheses, tendons and nails were performed by independent examiners blinded to each other's assessment.
A total of 57 children [26 girls (46%)] with a mean age of 9 years (s.d. 4) were divided into two groups, asymptomatic (Asy, 42 children) and symptomatic (Sy, 15 children), according to musculoskeletal pain. Differences were observed between the two groups in relation to age [9 years (s.d. 3) vs 11 years (s.d. 4), P < 0.05], PsO duration [2.4 years (s.d. 2.4) vs 5.4 years (s.d. 3.9), P < 0.001], systemic treatment [23 (54.8%) vs 2 [13.3%], P < 0.01], tender joint count [0 vs 12 children (80%), P < 0.001], swollen joint count [0 vs 3 children (20%), P < 0.01] and entheseal pain [0 vs 10 (66.7%), P < 0.001] in Asy and Sy children, respectively. US evaluation showed statistically significant differences between the Asy and Sy groups for the presence of US abnormalities [16/42 (38%) vs 12/15 (80%)], synovitis [1/42 (2%) vs 4/15 (25%)] and enthesitis [4/42 (9.5%) vs 5/15 (33%)]. Three children in the Sy group were classified with juvenile PsA (JPsA).
US abnormalities were higher in the Sy group, with synovitis and enthesitis as the most prevalent findings. Asy patients were more frequently under systemic treatment. US and a systematic clinical evaluation are useful tools for detecting subclinical JPsA in children with PsO and musculoskeletal symptoms.
评估患有皮肤银屑病(PsO)的儿童关节、关节周围结构及指甲的临床和超声(灰阶及多普勒)异常的患病率。
我们开展了一项横断面研究,纳入连续的患有PsO的儿童。由相互不知情的独立检查者对关节、起止点、肌腱和指甲进行系统的临床和超声评估。
根据肌肉骨骼疼痛情况,共57名儿童[26名女孩(46%)],平均年龄9岁(标准差4),被分为两组,无症状组(Asy,42名儿童)和有症状组(Sy,15名儿童)。两组在年龄[9岁(标准差3)对11岁(标准差4),P<0.05]、PsO病程[2.4年(标准差2.4)对5.4年(标准差3.9),P<0.001]、全身治疗情况[23例(54.8%)对2例(13.3%),P<0.01]、压痛关节计数[0对12名儿童(80%),P<0.001]、肿胀关节计数[0对3名儿童(20%),P<0.01]以及起止点疼痛[0对10例(66.7%),P<0.001]方面存在差异,分别为Asy组和Sy组儿童。超声评估显示,Asy组和Sy组在超声异常存在情况[16/42(38%)对12/15(80%)]、滑膜炎[1/42(2%)对4/15(25%)]和起止点炎[4/42(9.5%)对5/15(33%)]方面存在统计学显著差异。Sy组中有3名儿童被归类为青少年银屑病关节炎(JPsA)。
Sy组的超声异常情况更多见,滑膜炎和起止点炎是最常见的表现。Asy组患者接受全身治疗的频率更高。超声检查和系统的临床评估是检测患有PsO且有肌肉骨骼症状儿童亚临床JPsA的有用工具。