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  Vol. 123 No. 10, October 1987 TABLE OF CONTENTS
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Adult Kawasaki Syndrome

MAJ David F. Butler, MC; MAJ Douglas R. Hough, MC; MAJ Stephen J. Friedman, MC; COL Harry E. Davis, MC

Arch Dermatol. 1987;123(10):1356-1361.


Abstract

• Kawasaki syndrome (KS) is an idiopathic, acute, febrile, exanthemous illness that primarily affects infants and children. We describe a 20-year-old black woman who fulfilled the clinical criteria for the diagnosis of KS and excluded other possible causes. In addition, we reviewed data on 21 patients with adult KS reported in the English literature and accepted ten cases as representing this syndrome. The epidemiologic, clinical, laboratory, and pathologic features of the 11 cases representing adult KS are discussed. Although the initial reports of adult KS in the United States may have actually represented toxic shock syndrome, the occurrence of KS in adults should be acknowledged.

(Arch Dermatol 1987;123:1356-1361)



Author Affiliations

USA; USA; USA; USA

From the Dermatology (Drs Butler and Friedman), Rheumatology (Dr Hough), and General Medicine (Dr Davis) Services, Department of Medicine, William Beaumont Army Medical Center, El Paso, Tex.


Footnotes

Accepted for publication April 24, 1987.

The opinions or assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the Department of the Army or the Department of Defense.

Reprint requests to Dermatology Service, William Beaumont Army Medical Center, El Paso, TX 79920-5001 (Dr Butler).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Severe Thrombocytopenia as a Presenting Manifestation of Kawasaki Disease
Venglarcik et al.
Arch Pediatr Adolesc Med 1995;149:215-217.
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Adult Kawasaki Disease: Report of Two Cases Treated With Intravenous Gamma Globulin
Jackson et al.
Arch Intern Med 1994;154:1398-1405.
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