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Systemic-onset juvenile idiopathic arthritis or incomplete Kawasaki disease: a diagnostic challenge.

作者信息

Sahin Sezgin, Adrovic Amra, Barut Kenan, Kasapcopur Ozgur

机构信息

Department of Paediatric Rheumatology, Istanbul University, Cerrahpasa Medical Faculty, Istanbul, Turkey.

出版信息

Clin Exp Rheumatol. 2017 May-Jun;35 Suppl 104(2):10. Epub 2016 Oct 26.

PMID:27782865
Abstract
摘要

相似文献

1
Systemic-onset juvenile idiopathic arthritis or incomplete Kawasaki disease: a diagnostic challenge.全身型幼年特发性关节炎或不完全川崎病：诊断难题
Clin Exp Rheumatol. 2017 May-Jun;35 Suppl 104(2):10. Epub 2016 Oct 26.
2
Systemic-onset juvenile idiopathic arthritis and incomplete Kawasaki disease may belong to a single clinical syndrome within a spectrum of severity.全身型幼年特发性关节炎和不完全川崎病可能属于严重程度范围内的单一临床综合征。
Clin Exp Rheumatol. 2019 Nov-Dec;37 Suppl 122(6):3. Epub 2017 Oct 5.
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Failure to distinguish systemic-onset juvenile idiopathic arthritis from incomplete Kawasaki disease in an infant.婴儿期未能区分全身型幼年特发性关节炎与不完全川崎病。
J Paediatr Child Health. 2007 Oct;43(10):707-9. doi: 10.1111/j.1440-1754.2007.01189.x.
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Incomplete Kawasaki syndrome followed by systemic onset-juvenile idiopathic arthritis mimicking Kawasaki syndrome.不完全川崎病后继发全身型幼年特发性关节炎，类似川崎病。
Rheumatol Int. 2010 Feb;30(4):535-9. doi: 10.1007/s00296-009-0960-1. Epub 2009 May 20.
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Should 2016 Criteria for Macrophage Activation Syndrome be applied in children with Kawasaki disease, as well as with systemic-onset juvenile idiopathic arthritis?2016年巨噬细胞活化综合征的标准是否应适用于川崎病以及全身型幼年特发性关节炎患儿？
Ann Rheum Dis. 2016 Jul;75(7):e44. doi: 10.1136/annrheumdis-2016-209395. Epub 2016 Mar 10.
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Incomplete Kawasaki disease followed by systemic onset juvenile idiopathic arthritis- the diagnostic dilemma.不完全川崎病后继发全身型幼年特发性关节炎——诊断困境。
Indian J Pediatr. 2013 Sep;80(9):783-5. doi: 10.1007/s12098-012-0893-7. Epub 2012 Oct 10.
7
Comment on failure to distinguish systemic-onset juvenile idiopathic arthritis from incomplete Kawasaki disease in an infant.
J Paediatr Child Health. 2008 Nov;44(11):677-8; author reply 678. doi: 10.1111/j.1440-1754.2008.01402.x.
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Pathogenesis of systemic inflammatory diseases in childhood: "Lessons from clinical trials of anti-cytokine monoclonal antibodies for Kawasaki disease, systemic onset juvenile idiopathic arthritis, and cryopyrin-associated periodic fever syndrome".儿童系统性炎症性疾病的发病机制：“抗细胞因子单克隆抗体治疗川崎病、全身型幼年特发性关节炎及冷吡啉相关周期性发热综合征临床试验的经验教训”
Mod Rheumatol. 2015 Jan;25(1):1-10. doi: 10.3109/14397595.2014.902747. Epub 2014 May 20.
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Highly elevated serum levels of interleukin-18 in systemic juvenile idiopathic arthritis but not in other juvenile idiopathic arthritis subtypes or in Kawasaki disease: comment on the article by Kawashima et al.全身型幼年特发性关节炎患者血清白细胞介素-18水平显著升高，而其他幼年特发性关节炎亚型患者及川崎病患者则不然：对川岛等人文章的评论
Arthritis Rheum. 2002 Sep;46(9):2539-41; author reply 2541-2. doi: 10.1002/art.10389.
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Serum ferritin levels as a useful diagnostic marker for the distinction of systemic juvenile idiopathic arthritis and Kawasaki disease.血清铁蛋白水平作为一种有用的诊断标志物，可用于区分全身型幼年特发性关节炎和川崎病。
Mod Rheumatol. 2016 Nov;26(6):929-932. doi: 10.3109/14397595.2016.1159120. Epub 2016 Jul 19.

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Overlapping clinical features of systemic juvenile idiopathic arthritis and SARS-CoV-2-related multisystem inflammatory syndrome in children.儿童系统性幼年特发性关节炎与SARS-CoV-2相关多系统炎症综合征的重叠临床特征。
Reumatologia. 2023;61(1):63-70. doi: 10.5114/reum/161185. Epub 2023 Mar 8.
2
Predictors for Intravenous Immunoglobulin Resistance in Patients with Kawasaki Disease.川崎病患者静脉注射免疫球蛋白抵抗的预测因素。
Int J Clin Pract. 2022 Aug 3;2022:2726686. doi: 10.1155/2022/2726686. eCollection 2022.
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Low-Dose Prednisone Treatment for IVIG-Resistant Kawasaki Disease with Severe Arthritis and Joint Effusion in Two 3-Year-Old Children.
低剂量泼尼松治疗两名3岁儿童患有严重关节炎和关节积液的静脉注射免疫球蛋白抵抗性川崎病
Case Rep Pediatr. 2021 Apr 2;2021:6618346. doi: 10.1155/2021/6618346. eCollection 2021.
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Juvenile Idiopathic Arthritis.幼年特发性关节炎。
Balkan Med J. 2017 Apr 5;34(2):90-101. doi: 10.4274/balkanmedj.2017.0111.