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Coronary Artery Disease Affected by Moyamoya Disease - A case report -  

김학제 (고려대학교 구로병원 흉부외과학 교실)
조원민 (고려대학교 구로병원 흉부외과학 교실)
류세민 (고려대학교 구로병원 흉부외과학 교실)
황재준 (고려대학교 구로병원 흉부외과학 교실)
손영상 (고려대학교 구로병원 흉부외과학 교실)
최영호 (고려대학교 구로병원 흉부외과학 교실)
Publication Information
Journal of Chest Surgery / v.35, no.3, 2002 , pp. 231-234 More about this Journal
Abstract
Moyamoya disease is an unusual cerebrovascular disorder characterized by occlusive intimal dysplasia of the distal internal carotid and proximal cerebral arteries as well as other collateral arteries. However, moyamoya diseases are recently being reported as a systemic process. We experienced one case of coronary artery occlusive disease affected by moyamoya disease. The patient was a 35-year-old female, experiencing intermittent NYHA class ll dyspnea and exertional chest pain for 6 months and right paresthesia for 1 month before admission. Cerebral artery angiogram showed abnormal cerebrovascular systems and confirmed moyamoya disease with cerebral infarction of the left frontal lobe. In coronary artery angiogram, left coronary artery was not visualized due to total occlusion of the left main ostium and left coronary blood flow was supplied from normal right coronary artery. CABG was performed with OPCAB. Both internal mammary arteries were used for LAD and LCx. Intraoperative coronary artery findings showed intimal hyperplasia and no definite thrombi, and nondiseased coronary arteries were good and patent. We concluded that this patient's coronary artery disease was affected by moyamoya disease, and moyamoya disease should be evaluated in the extracerebral cardiovascular system.
Keywords
Moyamoya disease; Coronary artery disease;
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