天津医药

天津医药 ›› 2018, Vol. 46 ›› Issue (6): 670-672.doi: 10.11958/20180053

• 综述 • 上一篇    

川崎病休克综合征的临床研究进展

阚璇，吴德静，刘戈力   

  1. 天津医科大学总医院儿科（邮编300052）
  • 收稿日期:2018-01-10 修回日期:2018-03-16 出版日期:2018-06-15 发布日期:2018-07-05
  • 通讯作者: 刘戈力 E-mail:liugeli2001@126.com

Clinical research progress of Kawasaki disease shock syndrome

KAN Xuan, WU De-jing, LIU Ge-li   

  1. Department of Pediatric, Tianjin Medical University General Hospital, Tianjin 300052, China
  • Received:2018-01-10 Revised:2018-03-16 Published:2018-06-15 Online:2018-07-05
  • Contact: LIU Geli E-mail:liugeli2001@126.com

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摘要： 川崎病休克综合征（Kawasaki disease shock syndrome，KDSS）是川崎病的严重表现形式，是在诊断川崎病的基础上发生血流动力学不稳定状态而出现低灌注的临床症状，可以发生在川崎病的早期，极易漏诊和误诊，现就KDSS的临床特点、发病机制及治疗进行综述，旨在提高儿科临床医师早期识别该病的能力，减少其危及生命的并发症的发生。

关键词: 黏膜皮肤淋巴结综合征, 川崎病休克综合征, 综述

Abstract: Kawasaki disease shock syndrome (KDSS) is a serious manifestation of Kawasaki disease. It is a clinical symptom of hypoperfusion, which occurs hemodynamic instability on the basis of the diagnosis of Kawasaki disease. KDSS can occur in the early stage of Kawasaki disease, and can be easily missed and misdiagnosed. Now, the clinical features,pathogenesis and treatment of KDSS are reviewed, in order to improve the ability of clinical pediatricians to identify the disease early and reduce the occurrence of life-threatening complications.

Key words: mucocutaneous lymph node syndrome, Kawasaki disease shock syndrome, review