How not to Misdiagnose the Mild Forms of Mucopolysaccharidosis and Juvenile Idiopathic Arthritis.

IF 1.3 Q3 PEDIATRICS
Natalia V Buchinskaya, Nato D Vashakmadze, Natalia V Zhurkova, Lubov S Sorokina, Anastasia O Vechkasova, Liudmila K Mikhaylova, Leyla S Namazova-Baranova, Ekaterina Yu Zakharova, Valentina I Larionova, Dmitry O Ivanov, Mikhail M Kostik
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引用次数: 0

Abstract

Aims: The similarity between mucopolysaccharidosis (MPS) patients and juvenile idiopathic arthritis (JIA) leads to ineffective and needless anti-rheumatic treatment and delayed initiation of enzyme-replacement therapy, the early start of which is crucial for diminishing the disease progression and yielding better outcomes Background: The prevalence of joint involvement in the attenuated forms of MPS leads to the JIA misdiagnosis, especially in patients without distinctive facial dysmorphic features.

Objective: Our study aimed to compare mild forms of MPS and JIA and create a diagnostic score helping to differentiate both conditions.

Methods: 41 patients with mild forms of different types of MPS and 255 JIA patients with polyarthritis were included in the retrospective study. The routine clinical and laboratory features were used for the comparison analysis.

Results: The main features of the MPS cohort were younger age at the disease onset, lower weight and height lower inflammation, and higher number of affected joints compared to JIA patients and involvement in the organs and system, specific for MPS. The majority of the patients had similar C-reactive protein levels. At least two extra-articular features with polyarticular involvement were the main discriminating factors for both conditions. The sum (>38) of the following criteria:ESR< 12 mm/h (38 points), growth delay (height ≤ -2.0 SD; 20 points), age of joint involvement < 1.0 years (24 points), male sex (15 points), and involvement of both elbows with limited range of motion (29 points) can help in the differentiation If a patient had no extra-articular features, typical for MPS. The specificity and sensitivity of this model are 91.0% and 92.7% respectively.

Conclusion: This diagnostic algorithm might increase the suspicion of MPS and should be added to routine testing not miss the mild form of MPS inside JIA. Early diagnosis of mild cases allows for the initiation of treatment in patients with MPS at an earlier stage, which can significantly improve their daily functioning and quality of life.

如何避免误诊轻度粘多糖病和幼年特发性关节炎。
目的:粘多糖病(MPS)患者与幼年特发性关节炎(JIA)患者之间的相似性导致抗风湿治疗无效和不必要,延迟开始酶替代治疗,早期开始酶替代治疗对于减少疾病进展和获得更好的结果至关重要。减毒型MPS中关节累及的患病率导致JIA误诊,特别是在没有明显面部畸形特征的患者中。目的:我们的研究旨在比较轻度形式的MPS和JIA,并创建有助于区分这两种情况的诊断评分。方法:选取41例轻度不同类型MPS患者和255例JIA合并多发性关节炎患者进行回顾性研究。采用常规临床和实验室特征进行对比分析。结果:与JIA患者相比,MPS队列的主要特征是发病年龄更年轻,体重和身高更低,炎症程度更低,受影响关节数量更多,并且累及MPS特有的器官和系统。大多数患者的c反应蛋白水平相似。至少有两个关节外特征与多关节受累是这两种情况的主要鉴别因素。以下标准之和(>38):ESR< 12mm /h(38分),生长延迟(身高≤-2.0 SD;20分)、关节受累年龄< 1.0岁(24分)、男性(15分)和双肘受累但活动范围有限(29分)有助于鉴别。如果患者没有关节外特征,这是MPS的典型症状。该模型的特异性和敏感性分别为91.0%和92.7%。结论:该诊断方法可能增加对MPS的怀疑,应在常规检查中加入,不要漏诊JIA内轻度MPS。轻度病例的早期诊断允许在MPS患者的早期阶段开始治疗,这可以显着改善他们的日常功能和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
66
期刊介绍: Current Pediatric Reviews publishes frontier reviews on all the latest advances in pediatric medicine. The journal’s aim is to publish the highest quality review articles dedicated to clinical research in the field. The journal is essential reading for all researchers and clinicians in pediatric medicine.
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