评估幼年特发性关节炎患者的颞下颌关节受累情况。

IF 2.8 3区 医学 Q1 PEDIATRICS Pediatric Rheumatology Pub Date : 2024-11-25 DOI:10.1186/s12969-024-01031-w
Asena Pinar Sefer, Muferet Erguven
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引用次数: 0

摘要

目的:幼年特发性关节炎(JIA)是一种常见的儿童慢性炎症性风湿病。该病可影响全身所有滑膜关节。颞下颌关节(TMJ)是特发性关节炎的重要受累部位,经常受累,但由于受累部位通常没有症状,因此常常不被注意。本研究旨在确定本诊所收治的幼年特发性关节炎患者颞下颌关节受累的频率和风险因素,为早期诊断和治疗提供指导:方法:2014年1月至2017年5月期间在小儿风湿病门诊诊断为JIA并申请本研究的患者,在本门诊定期随访,有无障碍病史和风湿病综合门诊病历。纳入的患者均由放射科医生进行颞下颌关节磁共振成像(MRI)检查并出具报告:结果:在 41 名参与研究的患者中,51.2% 的患者颞下颌关节受累。研究发现,71.5%的颞下颌关节受累患者无症状,71.5%的患者为慢性受累。根据对比增强颞下颌关节磁共振成像结果,对有颞下颌关节受累和无颞下颌关节受累的患者进行比较;在有颞下颌关节受累的患者组中,多关节发病亚型的比例较高(P = 0.005),发病年龄较早(P = 0.003),病程较长(p = 0.037),受累关节较多(p = 0.005),ESR值较高(p = 0.0001),该组患者的治疗依从性和治疗反应较差(p = 0.001,p = 0.0001):颞下颌关节受累在JIA患者中很常见,可发生在疾病的任何阶段。结论:颞下颌关节受累在 JIA 患者中很常见,可发生在疾病的任何阶段,通常无症状且进展隐匿,在早期即导致下颌骨的慢性退行性病变。由于该病无症状、进展隐匿,而且有导致慢性、不可逆后遗症的风险,因此必须定期用造影剂增强颞下颌关节磁共振成像(TMJ MRI)筛查高风险的 JIA 患者,这仍然是金标准方法。虽然很难确定具体的风险因素,但有些因素可能会增加颞下颌关节受累的可能性。为了更好地识别这些高危患者并确定哪些人需要定期筛查,必须进行更大规模的多中心研究。
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Evaluation of temporomandibular joint involvement in juvenile idiopathic arthritis patients.

Objective: Juvenile idiopathic arthritis (JIA) is a common, chronic and inflammatory rheumatological disease of childhood. The disease can affect all synovial joints in the body. Temporomandibular joints (TMJs) are important areas of involvement in JIA, which are frequently involved but often not noticed because the involvement is usually asymptomatic. The aim of this study is to determine the frequency and risk factors of TMJ joint involvement in juvenile idiopathic arthritis patients admitted to our clinic, and to guide for early diagnosis and treatment.

Methods: Patients who applied to this study with the diagnosis of JIA between January 2014 and May 2017 at Pediatric Rheumatology Clinic, were followed up regularly in our clinic, had a accessible medical history, and a rheumatology polyclinic record. Patients with contrast-enhanced TMJ Magnetic Resonance Imaging (MRI) taken and reported by the radiologist were included.

Results: TMJ involvement was detected in 51.2% of the 41 patients included in the study. It was found that 71.5% of the patients with TMJ involvement were asymptomatic and 71.5% of the patients had chronic involvement. When the patients with and without TMJ involvement were compared according to the contrast-enhanced TMJ MRI results; In the patient group with involvement, the polyarticular onset subtype was seen at a higher rate (p = 0.005), the age of onset was earlier (p = 0.003), the disease duration was longer (p = 0.037), more joints were involved (p = 0.005), the ESR values ​​were higher (p = 0.0001), and the treatment compliance and treatment responses of the patients in this group were worse (p = 0.001, p = 0.0001).

Conclusion: TMJ involvement is common in JIA patients and can occur at any stage of the disease. It is often asymptomatic and progresses insidiously, leading to chronic and degenerative changes in the mandible at an early stage. Due to its asymptomatic nature, the insidious progression, and the risk of causing chronic, irreversible sequelae, it is crucial to screen high-risk JIA patients regularly with contrast-enhanced TMJ MRI, which remains the gold standard method. While specific risk factors are difficult to pinpoint, some factors may increase the likelihood of TMJ involvement. To better identify these high-risk patients and determine which individuals require regular screening, larger-scale and multicenter studies are essential.

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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
期刊最新文献
Real-world psychosocial impact among patients with juvenile idiopathic arthritis and families in Spain. Evaluation of temporomandibular joint involvement in juvenile idiopathic arthritis patients. The patient's voice: a cross-sectional study of physical health and disability in juvenile idiopathic arthritis. Pediatric case of immune-mediated necrotizing myopathy with anti-HMGCR antibodies and dermatomyositis skin rash. Epstein-Barr Virus encephalitis associated hemophagocytic lymphohistiocytosis in childhood-onset systemic lupus erythematosus: a case-based review.
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