Kawasaki disease shock syndrome (KDSS)

Main Article Content

Poomiporn Katanyuwong, MD

Abstract

Kawasaki disease (KD) is an acute febrile vasculitic syndrome of unknown etiology that occurs predominantly in infants and young children. The disease has also been called mucocutaneous lymph node syndrome or infantile periarteritis nodosa. Affected children present with high fever, rash, conjunctival injection, inflammation of the lips or oral cavity, cervical lymphadenitis, erythema and edema of the hands and feet. Cardiac sequelae, the most potentially life-threatening complications include coronary artery aneurysms or ectasia which can occur in up to 15-25% of untreated patients and may lead to myocardial infarction, sudden death, or ischemic heart disease.1

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How to Cite
1.
Katanyuwong P. Kawasaki disease shock syndrome (KDSS). BKK Med J [Internet]. 2012Feb.20 [cited 2020Sep.24];3(1):59. Available from: https://he02.tci-thaijo.org/index.php/bkkmedj/article/view/217913
Section
Case Report

References

1. Newburger JW, Takahashi M, Gerber MA, et al. Diagnosis, treatment, and long-term management of Kawasaki disease. A statement for health professionals from the committee on rheumatic fever, endocarditis and Kawasaki disease, council on cardiovascular disease in the young, American Heart Association. Circulation 2004;110:2747-71.
2. Kanegaye JT, Wilder MS, Molkara D, et al. Recognition of a Kawasaki disease shock syndrome. Pediatrics 2009; 123:783-9.