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1
Controversies in diagnosis and management of Kawasaki disease.川崎病诊断与治疗中的争议
World J Clin Pediatr. 2018 Feb 8;7(1):27-35. doi: 10.5409/wjcp.v7.i1.27.
2
Refractory Kawasaki Disease-a Challenge for the Pediatrician.难治性川崎病——儿科医生面临的挑战
SN Compr Clin Med. 2021;3(3):855-860. doi: 10.1007/s42399-021-00775-w. Epub 2021 Jan 28.
3
Kawasaki disease - A common childhood vasculitis.川崎病——一种常见的儿童血管炎。
Indian J Rheumatol. 2015 Dec;10:S78-S83. doi: 10.1016/j.injr.2015.07.010. Epub 2015 Oct 1.
4
Diagnosis of Kawasaki disease.川崎病的诊断
Int J Rheum Dis. 2018 Jan;21(1):36-44. doi: 10.1111/1756-185X.13224. Epub 2017 Nov 13.
5
State-of-the-art acute phase management of Kawasaki disease after 2017 scientific statement from the American Heart Association.2017年美国心脏协会科学声明发布后川崎病的最新急性期管理
Pediatr Neonatol. 2018 Dec;59(6):543-552. doi: 10.1016/j.pedneo.2018.03.005. Epub 2018 Mar 30.
6
Kawasaki disease: a comprehensive review of treatment options.川崎病:治疗选择的全面综述
J Clin Pharm Ther. 2015 Dec;40(6):620-5. doi: 10.1111/jcpt.12334. Epub 2015 Nov 7.
7
Systemic and pulmonary artery aneurysms in incomplete Kawasaki disease.不完全性川崎病中的体循环和肺动脉瘤
J Cardiol Cases. 2016 Mar 15;13(6):185-188. doi: 10.1016/j.jccase.2016.02.003. eCollection 2016 Jun.
8
[Kawasaki disease: what you need to know].[川崎病:你需要了解的内容]
Arch Pediatr. 2012 Nov;19(11):1264-8. doi: 10.1016/j.arcped.2012.07.005. Epub 2012 Aug 24.
9
Kawasaki disease in infants below 6 months: a clinical conundrum?6个月以下婴儿的川崎病:一个临床难题?
Int J Rheum Dis. 2016 Sep;19(9):924-8. doi: 10.1111/1756-185X.12854. Epub 2016 Mar 16.
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Preventing coronary artery lesions in Kawasaki disease.预防川崎病中的冠状动脉病变。
Biomed J. 2017 Jun;40(3):141-146. doi: 10.1016/j.bj.2017.04.002. Epub 2017 May 30.

引用本文的文献

1
Kawasaki disease: insights into the roles of T cells.川崎病:T细胞作用的见解
Front Immunol. 2025 Jul 17;16:1582638. doi: 10.3389/fimmu.2025.1582638. eCollection 2025.
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Exploring the role of exosomal and non-exosomal non-coding RNAs in Kawasaki disease: Implications for diagnosis and therapeutic strategies against coronary artery aneurysms.探索外泌体和非外泌体非编码RNA在川崎病中的作用:对冠状动脉瘤诊断和治疗策略的启示
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Imperative for long-term management and surveillance in Kawasaki disease.川崎病长期管理与监测的必要条件。
World J Clin Cases. 2025 Feb 6;13(4):99637. doi: 10.12998/wjcc.v13.i4.99637.
4
Ubiquitin ligase MDM2 mediates endothelial inflammation in Kawasaki disease vasculitis development.泛素连接酶MDM2在川崎病血管炎发展过程中介导内皮炎症。
Transl Pediatr. 2024 Feb 29;13(2):271-287. doi: 10.21037/tp-23-459. Epub 2024 Feb 27.
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Kawasaki disease and the environment: an enigmatic interplay.川崎病与环境:一种神秘的相互作用。
Front Immunol. 2023 Dec 18;14:1259094. doi: 10.3389/fimmu.2023.1259094. eCollection 2023.
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Dilemma in diagnosing incomplete Kawasaki disease in a resource limited setting.在资源有限的情况下诊断不完全川崎病的困境。
Ann Med Surg (Lond). 2023 Oct 2;85(11):5809-5812. doi: 10.1097/MS9.0000000000001380. eCollection 2023 Nov.
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Radiation dose analysis of computed tomography coronary angiography in Children with Kawasaki disease.川崎病患儿计算机断层扫描冠状动脉造影的辐射剂量分析
World J Clin Pediatr. 2023 Sep 9;12(4):230-236. doi: 10.5409/wjcp.v12.i4.230.
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Atypical Kawasaki Disease in a 16-Month-Old Baby: A Case Report and Literature Review.一名16个月大婴儿的非典型川崎病:病例报告及文献综述
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9
Emerging role of computed tomography coronary angiography in evaluation of children with Kawasaki disease.计算机断层扫描冠状动脉造影在川崎病患儿评估中的新作用。
World J Clin Pediatr. 2023 Jun 9;12(3):97-106. doi: 10.5409/wjcp.v12.i3.97.
10
Association of single nucleotide polymorphism rs113420705 of in children with Kawasaki disease from North India.印度北部川崎病患儿中 的单核苷酸多态性 rs113420705 的关联。
J Family Med Prim Care. 2022 Sep;11(9):5404-5409. doi: 10.4103/jfmpc.jfmpc_177_22. Epub 2022 Oct 14.

本文引用的文献

1
Computed Tomography Coronary Angiography for Evaluation of Children With Kawasaki Disease.计算机断层扫描冠状动脉造影术用于评估川崎病患儿
Curr Probl Diagn Radiol. 2018 Jul-Aug;47(4):238-244. doi: 10.1067/j.cpradiol.2017.09.013. Epub 2017 Oct 23.
2
The Clinical Utility and Safety of a New Strategy for the Treatment of Refractory Kawasaki Disease.一种治疗难治性川崎病新策略的临床效用与安全性
J Pediatr. 2017 Dec;191:140-144. doi: 10.1016/j.jpeds.2017.08.076.
3
What dose of aspirin should be used in the initial treatment of Kawasaki disease?川崎病初始治疗时应使用多大剂量的阿司匹林?
Arch Dis Child. 2017 Dec;102(12):1180-1182. doi: 10.1136/archdischild-2017-313538. Epub 2017 Oct 24.
4
[Neurological manifestations in atypical Kawasaki disease].[非典型川崎病的神经系统表现]
Rev Alerg Mex. 2017 Jul-Sep;64(3):376-380. doi: 10.29262/ram.v64i3.231.
5
Myocardial Assessment in School-Aged Children with Past Kawasaki Disease.对曾患川崎病的学龄儿童的心肌评估。
J Korean Med Sci. 2017 Nov;32(11):1835-1839. doi: 10.3346/jkms.2017.32.11.1835.
6
Gallbladder Hydrops Associated With Kawasaki Disease: A Case Report and Literature Review.川崎病相关的胆囊积水:一例报告及文献综述
Clin Pediatr (Phila). 2018 Mar;57(3):341-343. doi: 10.1177/0009922817696468. Epub 2017 Mar 1.
7
Pulmonary presentation of Kawasaki disease-A diagnostic challenge.川崎病肺部表现-诊断难题。
Pediatr Pulmonol. 2018 Jan;53(1):103-107. doi: 10.1002/ppul.23885. Epub 2017 Sep 26.
8
Clinical assessment of coronary arteries in Kawasaki disease: Focus on echocardiographic assessment.川崎病冠状动脉的临床评估:聚焦超声心动图评估
Congenit Heart Dis. 2017 Sep;12(5):636-640. doi: 10.1111/chd.12496. Epub 2017 Sep 18.
9
Acute Complete Adult-onset Kawasaki Disease in a Middle-Aged Woman.
J Coll Physicians Surg Pak. 2017 Aug;27(8):517-519.
10
Evaluation of longitudinal and radial left ventricular functions on 2-D and 3-D echocardiography before and after intravenous immunoglobulin in acute Kawasaki disease.急性川崎病患者静脉注射免疫球蛋白前后二维和三维超声心动图对左心室纵向和径向功能的评估
Pediatr Int. 2017 Dec;59(12):1229-1235. doi: 10.1111/ped.13423.

川崎病诊断与治疗中的争议

Controversies in diagnosis and management of Kawasaki disease.

作者信息

Pilania Rakesh Kumar, Bhattarai Dharmagat, Singh Surjit

机构信息

Department of Pediatrics, Advanced Pediatrics Centre, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh 160012, India.

出版信息

World J Clin Pediatr. 2018 Feb 8;7(1):27-35. doi: 10.5409/wjcp.v7.i1.27.

DOI:10.5409/wjcp.v7.i1.27
PMID:29456929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5803562/
Abstract

Kawasaki disease (KD) is a common medium vessel systemic vasculitis that usually occurs in small children. It has a predilection for the coronary arteries, but other medium sized arteries can also be involved. The etiology of this disorder remains a mystery. Though typical presentation of KD is quite characteristic, it may also present as incomplete or atypical disease in which case the diagnosis can be very challenging. As both incomplete and atypical forms of KD can be associated with serious coronary artery complications, the pediatrician can ill afford to miss these diagnoses. The American Heart Association has enunciated consensus guidelines to facilitate the clinical diagnosis and treatment of this condition. However, there are still several issues that remain controversial. Intravenous immunoglobulin remains the cornerstone of management but several other treatment modalities, especially glucocorticoids, are increasingly finding favour. We review here some of the contemporary issues, and the controversies thereon, pertaining to management of KD.

摘要

川崎病(KD)是一种常见的累及中等大小血管的全身性血管炎,通常发生于小儿。它好发于冠状动脉,但其他中等大小动脉也可受累。这种疾病的病因仍是个谜。虽然川崎病的典型表现颇具特征性,但它也可能表现为不完全或非典型疾病,在这种情况下诊断可能极具挑战性。由于川崎病的不完全和非典型形式都可能伴有严重的冠状动脉并发症,儿科医生绝不能漏诊这些病例。美国心脏协会已阐明了共识指南,以促进对该病的临床诊断和治疗。然而,仍有几个问题存在争议。静脉注射免疫球蛋白仍然是治疗的基石,但其他几种治疗方式,尤其是糖皮质激素,越来越受到青睐。我们在此回顾一些与川崎病治疗相关的当代问题及其争议。