Related Experiment Video
Updated: Jan 27, 2026

Signal Acquisition, Score Interpretation, and Economics of a Non-Invasive Point-of-Care Test for Coronary Artery Disease
Published on: August 9, 2024
Atypical Kawasaki disease: A patient with coronary, brain, and internal mammary arteritis
Azumi Hamasaki1, Tetsuro Uchida1, Yoshinori Kuroda1
1Second Department of Surgery, Yamagata University Faculty of Medicine, Yamagata, Japan.
Insights
This case study details atypical Kawasaki disease (KD) in a 25-year-old man, presenting with systemic arteritis affecting coronary, cerebral, and internal mammary arteries (IMAs). It highlights the first reported instance of KD involving the IMA.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Pediatric Cardiology
Background:
- Kawasaki disease (KD) typically affects children, causing inflammation in blood vessel walls.
- Systemic arteritis, a rare manifestation, can involve various arteries beyond the coronary arteries.
- Atypical presentations of KD require careful consideration for accurate diagnosis and management.
Observation:
- A 25-year-old male presented with angina pectoris, indicative of coronary artery disease.
- Coronary angiography revealed coronary artery aneurysms and triple-vessel disease.
- Cerebral angiography identified multiple small saccular aneurysms in the vertebral and posterior inferior cerebellar arteries.
Findings:
- The patient exhibited systemic arteritis involving coronary, cerebral, and internal mammary arteries (IMAs).
- Off-pump coronary artery bypass (OPCAB) grafting was performed, but bilateral IMAs were found non-patent due to adhesions.
- This case represents the first documented instance of Kawasaki disease affecting the IMAs.
Implications:
- This report expands the understanding of Kawasaki disease's potential vascular targets, including IMAs.
- Early recognition of atypical KD manifestations is crucial for timely intervention and preventing severe vascular complications.
- Further research into adult-onset KD and its diverse arterial involvements is warranted.
Abstract:
Here we report a rare case of atypical Kawasaki disease (KD) in a patient presenting with systemic arteritis affecting the coronary arteries, brain, and internal mammary arteries (IMAs). A 25-year-old man was referred to our institute with angina pectoris. Coronary angiography revealed coronary artery aneurysms and triple-vessel disease. Three-dimensional brain computed tomography showed multiple small saccular aneurysms on the vertebral and posterior inferior cerebellar arteries. Off-pump coronary artery bypass (OPCAB) grafting was performed; however, the bilateral IMAs were tightly adhered and not patent. OPCAB was completed using the bilateral radial and gastroepiploic arteries. This is the first report of KD involving the IMA.
Related Concept Videos
Coronary Artery Disease I: Introduction
Coronary Artery Disease II: Pathophysiology
Coronary Artery Disease V: Interprofessional Care
Antipsychotic Drugs: Typical and Atypical Agents
Coronary Artery Disease III: Clinical Manifestations
Coronary Artery Disease IV: Preventive Measures

