1. Features of Kawasaki disease at the extremes of age
- Author
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Joon-Sung Lee, Ji-W Han han, David Burgner, Kyung-Yil Lee, Ja-Hyun Hong, and Byung-Churl Lee
- Subjects
Male ,medicine.medical_specialty ,Pediatrics ,Mucocutaneous Lymph Node Syndrome ,Gastroenterology ,Group A ,Group B ,Cervical lymphadenopathy ,Internal medicine ,medicine ,Humans ,Leukocytosis ,Child ,Retrospective Studies ,Korea ,Thrombocytosis ,business.industry ,Gamma globulin ,Retrospective cohort study ,medicine.disease ,Child, Preschool ,Pediatrics, Perinatology and Child Health ,Female ,Kawasaki disease ,medicine.symptom ,business - Abstract
Aim: The diagnosis of Kawasaki disease (KD) in those outside the typical age range (6 months−4 years) is often delayed, potentially worsening prognosis. The features of KD in children ≤6 months and ≥5 years were compared with those presenting within the more typical age distribution. Methods: Korean children with complete diagnostic criteria for KD were grouped according to their age at presentation: Group A (≤6 months), Group B (7 months−4 years) and Group C (≥5 years). The clinical features, laboratory findings and outcome in each group were compared. Results: Of 136 children presenting to a single centre between 1999 and 2003, 10 children were in Group A, 114 in Group B and 12 in Group C. The mean total fever duration was 8 days in Group C and 6.2 days in Group A (P = 0.03). All children in Group C had cervical lymphadenopathy, compared with 50% of Group A and 64% of Group B (P = 0.01). Coronary artery lesions were commoner in older children (Group C, 42%) compared with Group B (17%, P = 0.05). All children had an equivalent leukocytosis, but Group C had significantly higher neutrophil counts (P = 0.001). Group A had significantly lower mean haemoglobin (P = 0.003) and total protein (P = 0.002) at presentation and a more marked thrombocytosis 1 week after intravenous immunoglobulin therapy (P
- Published
- 2006