INCIDENCE AND CLINICAL-FEATURES OF INCOMPLETE KAWASAKI-DISEASE

Citation
J. Fukushige et al., INCIDENCE AND CLINICAL-FEATURES OF INCOMPLETE KAWASAKI-DISEASE, Acta paediatrica, 83(10), 1994, pp. 1057-1060
Citations number
16
Categorie Soggetti
Pediatrics
Journal title
ISSN journal
08035253
Volume
83
Issue
10
Year of publication
1994
Pages
1057 - 1060
Database
ISI
SICI code
0803-5253(1994)83:10<1057:IACOIK>2.0.ZU;2-G
Abstract
During the nine-year period from 1983 to 1991, a total of 242 patients (142 males and 100 females) presenting with Kawasaki disease were see n at one hospital. Among them, 25 (10%) patients demonstrated incomple te Kawasaki disease and 17 of these 25 (68%) lacked two of the six pri ncipal symptoms of Kawasaki disease, with the most frequently missing symptoms being cervical lymphadenopathy and polymorphous exanthema. Th e typical laboratory features of Kawasaki disease, such as elevated er ythrocyte sedimentation rate, leukocytosis, anemia, positive C-reactiv e protein and thrombocytosis were also seen in the incomplete cases. N one of the 25 patients underwent iv gamma-globulin therapy while in 1 (4%), transient dilatation of the coronary artery was recognized. Inco mplete Kawasaki disease may therefore be characterized by a less frequ ent association of rash, cervical lymphadenopathy and coronary involve ment.