单冠状动脉异常合并严重左前降支狭窄:经皮介入治疗先天性右冠状动脉发育不全1例

Ofe Eugene Kwaku , Hao Luo , Cong Wen , Rongchuan Yue
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引用次数: 0

摘要

先天性右冠状动脉发育不全(RCA)是一种罕见的冠状动脉异常,可能与动脉粥样硬化性疾病共存,并提出了独特的诊断和治疗挑战。我们提出的情况下,60岁的妇女有10年的高血压史,经历难治性夜间心绞痛,尽管最佳的药物治疗。冠状动脉计算机断层血管造影(CCTA)显示先天性RCA发育不全和左前降支(LAD)近中部严重(70-80 %)狭窄。有创血管造影证实单冠状动脉系统(L-I型分类)伴严重(80-85 %)LAD狭窄。使用药物洗脱支架进行经皮冠状动脉介入治疗以缓解症状并恢复血流。在6个月的随访中,患者在指导治疗下仍无症状。该病例强调了两个关键点:(1)RCA发生通过迫使左冠状动脉系统在没有侧支补偿的情况下灌注扩大的心肌区域而加剧了动脉粥样硬化性LAD疾病的缺血;(2)PCI在解剖复杂的先天性异常中提供了有针对性的血供重建术。无创成像(CCTA)和有创血管造影仍然是描绘冠状动脉解剖和指导干预的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single coronary artery anomaly with critical left anterior descending artery stenosis: A case of percutaneous intervention in congenital right coronary artery agenesis
Congenital agenesis of the right coronary artery (RCA) is a rare coronary anomaly that may coexist with atherosclerotic disease and pose unique diagnostic and therapeutic challenges. We present the case of a 60-year-old woman with a 10-year history of hypertension who experienced refractory nocturnal angina despite optimal medical therapy. Coronary computed tomography angiography (CCTA) revealed congenital RCA agenesis and critical (70–80 %) narrowing of the proximal-to-mid left anterior descending artery (LAD). Invasive angiography confirmed a single coronary artery system (L-I type classification) with severe (80–85 %) LAD stenosis. Percutaneous coronary intervention using a drug-eluting stent was performed to resolve symptoms and restore flow. At 6-month follow-up, the patient remained asymptomatic on guideline-directed therapy. This case underscores two critical points: (1) RCA agenesis exacerbates ischemia in atherosclerotic LAD disease by forcing the left coronary system to perfuse an expanded myocardial territory without collateral compensation, and (2) PCI offers targeted revascularization in anatomically complex congenital anomalies. Noninvasive imaging (CCTA) and invasive angiography remain pivotal for delineating the coronary anatomy and guiding intervention.
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