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Published on: February 9, 2011
Atypical Kawasaki Disease in a 5-month-old Infant
Hiba Habeebu Rahiman1, Subhranshu Sekhar Kar1, Mariam Mehwish Mohsin1
1Department of Pediatrics, RAKCOMS, RAKMHSU, Ras-Al-khaimah, UAE.
Insights
Kawasaki disease (KD) in infants under 6 months presents diagnostic challenges. Early recognition and treatment of this vasculitis are vital to prevent serious cardiac complications like coronary aneurysms.
Area of Science:
- Pediatrics
- Cardiology
- Rheumatology
Background:
- Kawasaki disease (KD) is a critical vasculitis affecting young children.
- Infants under 6 months often exhibit atypical presentations, complicating diagnosis.
- Delayed diagnosis increases the risk of coronary artery aneurysms and other cardiac sequelae.
Purpose of the Study:
- To highlight the diagnostic challenges of Kawasaki disease in infants under 6 months.
- To emphasize the importance of early diagnosis and treatment in preventing cardiac complications.
- To report a rare case of incomplete Kawasaki disease in a 5-month-old infant.
Main Methods:
- Case report of a 5-month-old Bangladeshi girl with prolonged fever, rash, and sterile pyuria.
- Initial misdiagnosis of partially treated meningitis.
- Diagnosis confirmed by persistent inflammation, edema, osteoarthritis, and echocardiographic findings of a coronary aneurysm.
Main Results:
- The patient presented with atypical symptoms, delaying Kawasaki disease diagnosis.
- Echocardiography revealed a small coronary aneurysm.
- Treatment with intravenous immunoglobulin (IVIG), aspirin, and corticosteroids led to symptom resolution and normalized cardiac findings.
Conclusions:
- Kawasaki disease in infants under 6 months often presents as incomplete or atypical, posing diagnostic challenges.
- Prompt recognition and management, including echocardiography, are crucial for preventing cardiac complications.
- Increased clinical awareness and timely intervention are essential for improving outcomes in this high-risk population.
Abstract:
Kawasaki disease (KD) is an acute febrile vasculitis primarily affecting medium-sized arteries in children under 5 years. Infants under 6 months represent a diagnostic challenge due to atypical or incomplete presentations, increasing the risk of coronary artery lesions and complications such as aneurysms. Early diagnosis and treatment with intravenous immunoglobulin (IVIG) and aspirin are crucial to prevent long-term cardiac sequelae. We report a rare case of KD in a 5-month-old Bangladeshi girl presenting with prolonged fever, rash, and sterile pyuria. Initial evaluations pointed to partially treated meningitis, delaying KD diagnosis. Subsequent symptoms included edema, osteoarthritis, and persistent inflammation, leading to an echocardiographic detection of a small coronary aneurysm. Treatment with IVIG, aspirin, and corticosteroids resulted in the resolution of symptoms and normalization of cardiac findings. Infants below 6 months often present with incomplete KD, complicating diagnosis and delaying treatment. This case underscores the importance of considering KD in febrile infants with persistent inflammation, even in the absence of classic symptoms. Echocardiography and laboratory markers remain essential for early detection and management. Increased awareness and timely intervention in atypical and incomplete KD presentations are critical for reducing complications, particularly in high-risk groups like infants under 6 months.
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