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Published on: July 18, 2014
Acute myocardial infarction in an adolescent following recurrent Kikuchi-Fujimoto disease
Norifumi Yokoyama1, Taichi Miyazaki2, Ikko Oshiro2
1Department of Pediatrics, Gifu Municipal Hospital, Gifu, Japan f2001076gifu@yahoo.co.jp.
Abstract:
KFD is a benign self-limiting condition with rare complications. We herein report a case of an early adolescence boy who developed acute myocardial infarction (AMI) 15 months after his third episode of KFD. Each episode was characterised by fever and painful lymphadenopathy that resolved spontaneously. During the third episode, positron emission tomography-CT revealed widespread lymphadenopathy, including in the mediastinal nodes. Fifteen months later, the patient presented with sudden chest and shoulder pain. Cardiac catheterisation revealed multiple severe coronary artery stenoses, and percutaneous coronary intervention was performed. This is the first reported paediatric case of AMI potentially linked to prior recurrent episodes of KFD. Chronic or subclinical inflammation around the coronary arteries may have contributed to early onset atherosclerosis. KFD is generally self-limiting but may involve long-term vascular consequences in recurrent or atypical cases.
Insights
Recurrent KFD (Kawasaki disease-like fever) may lead to rare complications. A case report details a child experiencing acute myocardial infarction (AMI) 15 months after recurrent KFD episodes, suggesting potential long-term vascular risks.
Area of Science:
- Pediatrics
- Cardiology
- Rheumatology
Background:
- Kawasaki disease-like fever (KFD) is typically a benign, self-limiting illness.
- Complications are rare, but recurrent or atypical KFD may pose long-term risks.
- The potential for KFD to cause chronic vascular inflammation is not well-established.
Purpose of the Study:
- To report the first pediatric case of acute myocardial infarction (AMI) potentially linked to recurrent KFD.
- To highlight the possibility of long-term vascular consequences following KFD.
Main Methods:
- Case report of an early adolescent male.
- Detailed clinical history including recurrent episodes of fever and lymphadenopathy.
- Diagnostic imaging: Positron Emission Tomography-CT (PET-CT) for lymphadenopathy.
- Cardiac catheterization to assess coronary artery status.
- Percutaneous coronary intervention (PCI) for management of coronary stenoses.
Main Results:
- The patient experienced three episodes of KFD characterized by fever and painful lymphadenopathy.
- PET-CT during the third episode showed widespread lymphadenopathy, including mediastinal involvement.
- Fifteen months after the third KFD episode, the patient presented with acute chest and shoulder pain.
- Cardiac catheterization revealed severe coronary artery stenoses, necessitating PCI.
Conclusions:
- This case suggests a potential association between recurrent KFD and the development of AMI in a pediatric patient.
- Chronic or subclinical inflammation secondary to KFD may contribute to early-onset atherosclerosis.
- Recurrent or atypical KFD warrants consideration for potential long-term vascular sequelae.
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