Abstract
We report three patients who initially showed prolonged fever, lung parenchymal consolidation and laboratory findings of pneumonia, and secondarily presented a clinical picture ascribed to Kawasaki syndrome. Two of these children developed coronary artery dilations, which regressed upon echocardiography after 12 months. In the case of infants showing broncho-pulmonary abnormalities with slow resolution, active inflammatory parameters and high fever persistence, pediatricians should consider atypical Kawasaki syndrome as a possible alternative diagnosis.
Lingua originale | English |
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pagine (da-a) | 1373-1376 |
Numero di pagine | 4 |
Rivista | Rheumatology International |
Volume | 2009 |
Stato di pubblicazione | Pubblicato - 2008 |
Keywords
- Kawaski syndrome
- Pneumonia