Karadağ Şerife Gül, Coskuner Taner, Demirkan Fatma Gül, Sonmez Hafize Emine, Ozdel Semanur, Çakan Mustafa, Otar Yener Gulcin, Ozturk Kubra, Demir Ferhat, Sozeri Betül, Aktay Ayaz Nuray
Department of Pediatric Rheumatology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Department of Pediatric Rheumatology, University of Health Sciences, Ümraniye Research and Training Hospital, Istanbul, Turkey.
Rheumatology (Oxford). 2024 Sep 1;63(SI2):SI160-SI166. doi: 10.1093/rheumatology/kead496.
To describe the clinical features and treatment outcomes of children with juvenile psoriatic arthritis (JPsA) and compare the distinct patterns of the disease between early-onset and late-onset age groups.
Patients with JPsA followed regularly for at least 6 months between 2010 and 2020 in seven paediatric rheumatology centres in Turkey were included in the study. The demographic features, clinical manifestations, treatment strategies and outcomes of the patients were evaluated retrospectively.
A total of 87 (46 male/41 female) patients were included in the study. The mean age at diagnosis was 11.9 years (s.d. 4.5). Fifty-seven (65.5%) patients had psoriasis at the time of diagnosis and arthritis preceded psoriasis in 10 (11.5%) patients. Thirty (34.5%) patients had dactylitis, 28 (32.2%) had nail pitting, 36 (41.4%) had involvement of the small joints and 20 (23%) had enthesitis. Sacroiliitis was detected in 11 (12.6%) patients by MRI. ANA was positive in 35 (40.2%) patients. Twelve children (13.8%) were in the early-onset (<5 years) group. Uveitis and ANA positivity were more common in the early-onset group. Active joint counts and activity scores of our patients showed significant improvement at month 6 and at the last control compared with baseline.
About one-third of patients with JPsA do not have psoriasis at the time of diagnosis. In some patients, no skin lesion is seen during the course of the disease. Children with PsA seem to display two different phenotypes. Younger children have a female predominance, ANA positivity and uveitis, while older children have more axial involvement.
描述青少年银屑病关节炎(JPsA)患儿的临床特征和治疗结果,并比较早发型和晚发型年龄组之间该疾病的不同模式。
纳入2010年至2020年期间在土耳其七个儿科风湿病中心定期随访至少6个月的JPsA患者。对患者的人口统计学特征、临床表现、治疗策略和结果进行回顾性评估。
共纳入87例患者(46例男性/41例女性)。诊断时的平均年龄为11.9岁(标准差4.5)。57例(65.5%)患者在诊断时有银屑病,10例(11.5%)患者关节炎先于银屑病出现。30例(34.5%)患者有指(趾)炎,28例(32.2%)有甲凹点,36例(41.4%)有小关节受累,20例(23%)有附着点炎。MRI检查发现11例(12.6%)患者有骶髂关节炎。35例(40.2%)患者ANA阳性。12名儿童(13.8%)属于早发型(<5岁)组。葡萄膜炎和ANA阳性在早发型组中更常见。与基线相比,我们患者的活动关节计数和活动评分在第6个月和最后一次随访时显示出显著改善。
约三分之一的JPsA患者在诊断时没有银屑病。在一些患者中,病程中未出现皮肤病变。PsA患儿似乎表现出两种不同的表型。年龄较小的儿童以女性为主,ANA阳性且有葡萄膜炎,而年龄较大的儿童有更多的中轴受累。