Al Naabi Hanan, Al Lawati Hatim
Internal Medicine Residency Program, Oman Medical Specialty Board, Muscat, Oman.
Division of Cardiology, Department of Medicine, Sultan Qaboos University Hospital, Muscat, Oman.
Oman Med J. 2017 Jul;32(4):344-348. doi: 10.5001/omj.2017.65.
Spontaneous coronary artery dissection (SCAD) is a rare condition that is often underdiagnosed given limitations of conventional cineangiography. In addition to the diagnostic challenge, the condition poses a major therapeutic dilemma given paucity of literature to guide management. We report the case of a 55-year-old woman, who presented with acute coronary syndrome. Coronary angiography at the time of the index hospitalization revealed type 2 SCAD. She was managed conservatively. Repeat coronary angiography three months later showed complete resolution of the previously noted dissection. Because of the high association between SCAD and fibromuscular dysplasia (FMD), a cross-sectional imaging was performed in this case, which ruled out underlying FMD. The patient has been followed longitudinally since her index event and has had no reported recurrences.
自发性冠状动脉夹层(SCAD)是一种罕见疾病,鉴于传统血管造影的局限性,其常常未被诊断出来。除了诊断方面的挑战外,由于缺乏指导治疗的文献,这种疾病还带来了重大的治疗困境。我们报告了一例55岁女性,她因急性冠状动脉综合征就诊。首次住院时的冠状动脉造影显示为2型SCAD。她接受了保守治疗。三个月后重复冠状动脉造影显示,先前发现的夹层已完全消退。由于SCAD与纤维肌性发育异常(FMD)之间存在高度关联,因此对该病例进行了横断面成像检查,排除了潜在的FMD。自首次发病以来,该患者一直接受长期随访,未报告有复发情况。