Two cases of Kawasaki disease: Clinical characteristics and onset of fever and gastrointestinal symptoms

Background Kawasaki disease (KD) is a prevalent form of systemic vasculitis that can damage various organs and systems in children. Typical KD not difficult to diagnose clinical practice. In recent years, it has been shown an increasing number children do satisfy the diagnostic criteria for typical KD. This condition known as incomplete (IKD). It challenging promptly treat such Case Description A 10-year-old girl was admitted hospital due fever abdominal pain. She presented with shock symptoms. An enhanced computed tomography scan revealed intestinal pneumatosis, effusion, gallbladder enlargement, indicating obstruction. Due poor outcome following emergency laparoscopic cholecystectomy, IKD suspected. 3-month-old male pediatric patient fever. Patchy, congestive rashes formed on patient's body progressed. suspected based signs fever, rash, hyperemia lips. The two patients were then treated human immunoglobulin aspirin treatment. prognosis favorable prompt Conclusion fact frequently misdiagnosed, vital (1) improve early identification prolonged anti-infection failure initial manifestation (2) perform timely diagnosis comprehensive