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唐氏综合征的关节病:一种被低估的炎症性关节疾病,值得更名。

Arthropathy of Down syndrome: an under-diagnosed inflammatory joint disease that warrants a name change.

机构信息

National Centre for Paediatric Rheumatology, Our Lady's Children's Hospital, Crumlin, Ireland.

National Children's Research Centre, Dublin, Ireland.

出版信息

RMD Open. 2019 Jun 3;5(1):e000890. doi: 10.1136/rmdopen-2018-000890. eCollection 2019.

DOI:10.1136/rmdopen-2018-000890
PMID:31245048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6560675/
Abstract

UNLABELLED

There is an increased incidence and prevalence of arthropathy in children with Down syndrome. However, it is rarely reported or recognised at onset, and remains under-diagnosed. Children with arthropathy of Down syndrome (A-DS) are presenting with significant joint damage and disability at diagnosis.

OBJECTIVE

To identify undiagnosed cases of A-DS and document time to diagnosis. Also to describe clinical, laboratory and radiological features of A-DS at diagnosis.

METHODOLOGY

Children with Down syndrome (DS) (0-21 years) were invited to attend a musculoskeletal screening clinic. A second physician at a further clinic confirmed suspected cases of A-DS. Investigations and treatment were instigated as per normal clinical practice for Juvenile idiopathic arthritis (JIA). Data on a convenience sample of 21 newly diagnosed children with JIA was collected to create a comparison group.

RESULTS

Over an 18-month period, 503 children with DS were screened for arthritis and 18 new cases diagnosed. In total, 33 children were identified with A-DS (combining cases attending pre-dating commencement of the study and those referred to our centre during the study period). This suggests prevalence of A-DS is 20/1000. A significant delay in diagnosis of A-DS was observed. The majority of children presented with polyarticular-rheumatoid factor-negative arthritis, with predominance in the small joints of the hands and wrists. Erosive changes were reported on X-ray in a significantly greater proportion (42%) of children with A-DS than JIA (14%). MRI was used to confirm diagnosis in four cases.

CONCLUSION

Children with DS are at increased risk of arthritis. Future research to accurately define disease pathogenesis and identify a biomarker of disease would be of benefit.

摘要

未注明

唐氏综合征儿童的关节病发病率和患病率增加。然而,它在发病时很少被报道或认识,并且仍然被误诊。唐氏综合征伴有关节病(A-DS)的儿童在诊断时就出现了严重的关节损伤和残疾。

目的

确定未确诊的 A-DS 病例,并记录诊断时间。还描述了 A-DS 在诊断时的临床、实验室和影像学特征。

方法

邀请唐氏综合征(DS)(0-21 岁)儿童参加肌肉骨骼筛查诊所。另一位医生在进一步的诊所确认疑似 A-DS 病例。根据青少年特发性关节炎(JIA)的常规临床实践进行了检查和治疗。收集了便利样本中 21 例新诊断的 JIA 儿童的数据,以创建一个对照组。

结果

在 18 个月的时间里,对 503 名 DS 儿童进行了关节炎筛查,发现了 18 例新病例。共有 33 名儿童被诊断为 A-DS(包括在研究开始前就诊和研究期间转介到我们中心的病例)。这表明 A-DS 的患病率为 20/1000。A-DS 的诊断明显延迟。大多数儿童表现为多关节炎-类风湿因子阴性关节炎,以手部和手腕小关节为主。在 A-DS 中,X 线报告的侵蚀性改变比例明显高于 JIA(42%对 14%)。在 4 例中使用 MRI 确认了诊断。

结论

DS 儿童患关节炎的风险增加。未来的研究需要准确定义疾病发病机制并确定疾病的生物标志物,这将是有益的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/1ec9be3ee0e4/rmdopen-2018-000890f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/4a01276da3cc/rmdopen-2018-000890f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/2331ef56cbfc/rmdopen-2018-000890f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/f653f092b169/rmdopen-2018-000890f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/57c3c60a4b6b/rmdopen-2018-000890f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/1ec9be3ee0e4/rmdopen-2018-000890f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/4a01276da3cc/rmdopen-2018-000890f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/2331ef56cbfc/rmdopen-2018-000890f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/f653f092b169/rmdopen-2018-000890f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/57c3c60a4b6b/rmdopen-2018-000890f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf2/6560675/1ec9be3ee0e4/rmdopen-2018-000890f05.jpg

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