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剥脱性骨软骨炎在幼年特发性关节炎患者中表现出严重的病程和较差的预后:22 例配对研究。

Osteochondritis dissecans shows a severe course and poor outcome in patients with juvenile idiopathic arthritis: a matched pair study of 22 cases.

机构信息

Department of Orthopaedics, Medical Faculty, University of Duesseldorf, Moorenstr. 5, 40225, Düsseldorf, Germany.

Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Centre for Child and Adolescent Health, University of Duesseldorf, Moorenstr. 5, 40225, Düsseldorf, Germany.

出版信息

Rheumatol Int. 2018 Sep;38(9):1705-1712. doi: 10.1007/s00296-018-4100-7. Epub 2018 Jul 10.

Abstract

Juvenile osteochondritis dissecans (JOCD) and juvenile idiopathic arthritis (JIA) are both common diseases which may affect joints and bony structures in pediatric patients. In some cases, JOCD and JIA occur at the same time. In this study, the course of JOCD in patients with JIA was therefore evaluated to provide possible recommendations for further treatment opportunities and control examinations. From 06/2012 to 03/2018 55 children with JOCD with or without JIA were examined. Inclusion criteria were: (1) age ≤ 16 years, (2) diagnosis of a JOCD with or without JIA and (3) two routine MRI controls. The JOCD evaluation based on the classification according to Bruns and the measurement of the largest extent via MRI. 18 of these 55 children met our criteria: 11 JOCD findings of 7 patients with JIA (group A) were matched according to age and localization of JOCD to 11 patients without JIA (group B). Mean age of disease onset of JIA was 8.2 years (oligo JIA) and of JOCD 11.6 years. The mean time follow-up was 17.7 months. At all observation time points more JOCD findings (with stage III° and IV°, respectively) along with a significant deterioration was seen in group A compared to group B. The comparison of the last MRI control between group A and group B shows a significant smaller defect size (decrease of 54.5%, p = 0.028) in group B (97.9 ± 48.9 mm) as in group A (185.1 ± 102.9 mm). In comparison of first (169.7 ± 84.2 mm) and last MRI (97.9 ± 48.9 mm) a significant decrease in lesion size of JOCD in group B was seen (decrease of 58.4%, p = 0.048). Patients with JIA show a more progressive and severe course of JOCD. Therefore, we recommend (1) the early use of MRI in patients with JIA and persistent joint pain to detect potential JOCD and (2) in presence of JIA and JOCD regular MRI follow-up controls to identify deteriorating JOCD findings and prevent early joint destruction in pediatric patients.

摘要

青少年剥脱性骨软骨炎(JOCD)和青少年特发性关节炎(JIA)都是常见的疾病,可能影响儿科患者的关节和骨骼结构。在某些情况下,JOCD 和 JIA 同时发生。在这项研究中,评估了 JIA 患者的 JOCD 病程,为进一步的治疗机会和控制检查提供了可能的建议。

2012 年 6 月至 2018 年 3 月,对 55 例 JOCD 患儿(伴或不伴 JIA)进行了检查。纳入标准为:(1)年龄≤16 岁,(2)诊断为 JOCD 伴或不伴 JIA,(3)两次常规 MRI 检查。JOCD 的评估基于 Bruns 分类和 MRI 测量的最大程度。55 例患儿中,18 例符合我们的标准:7 例 JIA 患儿(A 组)的 11 例 JOCD 结果根据年龄和 JOCD 定位与 11 例无 JIA 患儿(B 组)相匹配。JIA 发病的平均年龄为 8.2 岁(寡 JIA),JOCD 为 11.6 岁。平均随访时间为 17.7 个月。在所有观察时间点,A 组 JOCD 病变(分别为 III°和 IV°)较多,且病情明显恶化。A 组和 B 组最后一次 MRI 检查比较显示,B 组缺陷尺寸明显减小(减少 54.5%,p=0.028)(97.9±48.9mm),而 A 组(185.1±102.9mm)。与第一次(169.7±84.2mm)和最后一次 MRI(97.9±48.9mm)相比,B 组 JOCD 病变明显减小(减少 58.4%,p=0.048)。

JIA 患儿 JOCD 病情进展更为严重。因此,我们建议:(1)对持续关节疼痛的 JIA 患儿及早使用 MRI 以发现潜在的 JOCD;(2)在存在 JIA 和 JOCD 的情况下,定期进行 MRI 随访检查,以发现 JOCD 病变恶化情况,防止儿科患者早期关节破坏。

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