| 英文摘要 |
Kawasaki disease (KD) is a systemic inflammatory vasculitis characterized by fever, conjunctivitis, mucosal inflammation, skin rash, changes in the extremities, and cervical lymphadenopathy. These clinical features form the basis of the diagnostic criteria for KD. Patients who do not meet the classic diagnostic criteria may be classified as having incomplete Kawasaki disease (IKD). In recent years, the term IKD has been used to describe cases with incomplete clinical manifestations, regardless of the presence of coronary artery involvement. Importantly, the risk of coronary artery complications in IKD is comparable to, and may even exceed, that observed in classic KD. However, the diagnosis of IKD remains challenging and is often delayed, particularly in infants and young children. To aid in early identification, several diagnostic algorithms incorporating clinical features, echocardiographic findings, and laboratory parameters have been developed. Based on established diagnostic criteria, we report the case of a six-month-old female infant diagnosed with IKD on the fifth day of fever who was promptly treated with intravenous immunoglobulin. When a strong clinical suspicion of KD is present, pediatricians should consider the diagnosis even before five days of fever have elapsed and initiate treatment as early as possible, especially in infants aged six months or younger. This case highlights the critical importance of early recognition and timely intervention in preventing coronary artery complications. |