Negoro Nobuyuki, Nariyama Jin, Nakagawa Atsushi, Katayama Hiroshi, Okabe Taichi, Hazui Hiroshi, Yokota Naohito, Kojima Shigeyuki, Hoshiga Masaaki, Morita Hiroshi, Ishihara Tadashi, Hanafusa Toshiaki
First Department of Internal Medicine, Osaka Medical College, Takatsuki City, Japan.
Circ J. 2003 Apr;67(4):362-5. doi: 10.1253/circj.67.362.
Acute coronary syndrome occurred in 2 young adults who had a history of Kawasaki disease (KD), but few other coronary risk factors. The first patient was a 27-year-old male with acute myocardial infarction without stenosis detected by coronary arteriography 4 years earlier. Emergency coronary arteriography showed occlusion of the right coronary artery. Aspiration-thrombectomy and rescue balloon angioplasty were successfully performed. The second patient was a 32-year-old male with unstable angina. Right coronary arteriography showed total occlusion with severe calcification. Left coronary arteriography showed 99% stenosis at the proximal site of the circumflex artery, and a directional coronary atherectomy was performed. Histological examination of a specimen from this site revealed a lipid core, macrophages, and smooth muscle cells. Restenosis was not observed on follow-up coronary arteriography after 5-6 months in either case. The coronary stenosis in each case was probably caused by accelerated atherosclerosis at the site without aneurysm as it seemed to be 'normal' on arteriography. Conventional catheter intervention was effective treatment. The sequelae of KD should be recognized as independent coronary risk factors.
2名有川崎病(KD)病史但几乎没有其他冠状动脉危险因素的年轻成人发生了急性冠状动脉综合征。首例患者为一名27岁男性,4年前冠状动脉造影未发现狭窄,却发生了急性心肌梗死。急诊冠状动脉造影显示右冠状动脉闭塞。成功实施了抽吸血栓切除术和补救性球囊血管成形术。第二例患者为一名32岁男性,患有不稳定型心绞痛。右冠状动脉造影显示完全闭塞并伴有严重钙化。左冠状动脉造影显示回旋支动脉近端99%狭窄,遂进行了定向冠状动脉斑块旋切术。对该部位标本进行组织学检查发现有脂质核心、巨噬细胞和平滑肌细胞。5-6个月后随访冠状动脉造影,两例均未观察到再狭窄。在每种情况下,冠状动脉狭窄可能是由动脉造影时看似“正常”的无动脉瘤部位的动脉粥样硬化加速所致。传统的导管介入治疗是有效的治疗方法。KD的后遗症应被视为独立的冠状动脉危险因素。