Polyarteritis nodosa mimics Kawasaki disease
Ibrahim Alibrahim1, Aisha Mirza2, Amer Khojah3
1Umm Al-Qura University College of Medicine, Makkah, Saudi Arabia.
BMJ Case Reports
|October 21, 2024
Summary
Polyarteritis nodosa (PAN), a rare vasculitis, can mimic Kawasaki disease (KD) in children, presenting with coronary artery aneurysms. Early consideration of PAN is crucial for accurate diagnosis and effective treatment, even with KD-like symptoms.
Area of Science:
- Pediatric Rheumatology
- Cardiology
- Vasculitis Research
Background:
- Polyarteritis nodosa (PAN) is a rare vasculitis affecting small to medium arteries, with diverse clinical presentations.
- Cardiac involvement in pediatric PAN can include pericarditis, valvular disease, and coronary artery aneurysms.
- Kawasaki disease (KD) is a common childhood vasculitis frequently associated with coronary artery abnormalities.
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