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Systemic-onset juvenile idiopathic arthritis and incomplete Kawasaki disease may belong to a single clinical syndrome within a spectrum of severity.

作者信息

Han Seung Beom, Lee Soo Young

机构信息

Department of Paediatrics, The Catholic University of Korea, Seoul, Republic of Korea.

出版信息

Clin Exp Rheumatol. 2019 Nov-Dec;37 Suppl 122(6):3. Epub 2017 Oct 5.

PMID:28980895
Abstract
摘要

相似文献

1
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.
2
Systemic onset juvenile idiopathic arthritis with macrophage activation syndrome misdiagnosed as Kawasaki disease: case report and literature review.以巨噬细胞活化综合征为表现的全身型幼年特发性关节炎误诊为川崎病：病例报告及文献复习。
Rheumatol Int. 2013 Apr;33(4):1065-9. doi: 10.1007/s00296-010-1650-8. Epub 2010 Dec 5.
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Systemic onset juvenile idiopathic arthritis with macrophage activation syndrome and coronary artery dilatation misdiagnosed as Kawasaki disease.全身型幼年特发性关节炎合并巨噬细胞活化综合征及冠状动脉扩张误诊为川崎病。
Turk J Pediatr. 2015 Sep-Oct;57(5):518-21.
4
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.
5
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.
6
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.
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.
8
Diagnosis of systemic-onset juvenile idiopathic arthritis after treatment for presumed Kawasaki disease.在对疑似川崎病进行治疗后诊断为全身型幼年特发性关节炎。
J Pediatr. 2015 May;166(5):1283-8. doi: 10.1016/j.jpeds.2015.02.003. Epub 2015 Mar 11.
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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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Coronary artery abnormalities in children with systemic-onset juvenile idiopathic arthritis.儿童全身型幼年特发性关节炎的冠状动脉异常。
Joint Bone Spine. 2014 May;81(3):257-9. doi: 10.1016/j.jbspin.2013.09.004. Epub 2014 May 1.

引用本文的文献

1
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
Under-Recognized Macrophage Activation Syndrome in Refractory Kawasaki Disease: A Wolf in Sheep's Clothing.难治性川崎病中未被充分认识的巨噬细胞活化综合征：披着羊皮的狼。
Children (Basel). 2022 Oct 20;9(10):1588. doi: 10.3390/children9101588.
3
Severe Recurrent Fever Episodes With Clinical Diagnosis of Hemophagocytic Lymphohistiocytosis, Incomplete Kawasaki Disease and Systemic-Onset Juvenile Idiopathic Arthritis: A Case Report and Literature Review.
临床诊断为噬血细胞性淋巴组织细胞增生症、不完全川崎病和全身型幼年特发性关节炎的严重反复发热发作：一例报告及文献综述
Front Pediatr. 2020 Mar 10;8:93. doi: 10.3389/fped.2020.00093. eCollection 2020.