This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow P3Rs: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when P3Rs are posted
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shibuya, N.
Right arrow Articles by Yanagisawa, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shibuya, N.
Right arrow Articles by Yanagisawa, M.
Related Collections
Right arrow Infectious Disease & Immunity
Right arrowRelated AAP Red Book topics:
Kawasaki Disease (Mucocutaneous...
Group A Streptococcal Infections
PEDIATRICS Vol. 110 No. 2 August 2002, pp. e17-e17


ELECTRONIC ARTICLE

Kawasaki Disease Before Kawasaki at Tokyo University Hospital

Noriko Shibuya, MD*, Kazuhiko Shibuya, MD{ddagger}, Hitoshi Kato, MD{ddagger} and Masayoshi Yanagisawa, MD§

* Department of Pediatrics, Sanno Hospital, Tokyo, Japan
{ddagger} Department of Pediatrics, Graduate School of Medicine, University of Tokyo, Tokyo, Japan
§ Department of Pediatrics, National Children’s Medical Center, Tokyo, Japan

Objective. Kawasaki disease (KD) was first reported by Tomisaku Kawasaki in 1967 in Japan. Large-scale nationwide epidemiologic surveys have been conducted continuously by the Japan Kawasaki Disease Research Committee; however, there were very few reports of KD before 1967. This study was performed to clarify when KD appeared in Japan.

Design. We investigated the medical charts of patients who had been hospitalized at Tokyo University Hospital between 1940 and 1965.

Results. We identified 10 patients whose clinical signs fulfilled the criteria for KD. The ages of the patients ranged from 8 months to 5 years, and their final diagnoses were Stevens-Johnson syndrome, allergic toxic erythema, Izumi fever, scarlet fever, and cervical lymphadenitis. These 10 patients presented between 1950 and 1964, and no confirmed cases were seen between 1940 and 1949.

Conclusions. Our findings suggested that KD patients were rare before 1950 in Japan.

Key Words: Kawasaki disease • Stevens-Johnson syndrome • allergic toxic erythema • Izumi fever • scarlet fever

Abbreviations: KD, Kawasaki disease


Received for publication Sep 26, 2001; Accepted Apr 29, 2002.