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放射治疗后左冠状动脉开口狭窄:临床与组织学研究

Post-radiotherapeutic left main coronary ostial stenosis: clinical and histological study.

作者信息

Grollier G, Commeau P, Mercier V, Lognoné T, Gofard M, Scanu P, Maiza D, Mandard J C, Foucault J P, Potier J C

机构信息

Service de Cardiologie, CHU Cote de Nacre, Caen, France.

出版信息

Eur Heart J. 1988 May;9(5):567-70. doi: 10.1093/oxfordjournals.eurheartj.a062546.

Abstract

Pericardial abnormalities remain the most common manifestation of radiation-induced cardiac disease, but coronary artery lesions are not rare. In this report we describe a left coronary ostial stenosis which appeared five years after mediastinal irradiation for breast carcinoma in a 50-year-old woman. The patient underwent coronary angiography. A pressure drop was observed as the left catheter tip engaged the left coronary ostium; so, only nonselective coronary opacifications were performed showing an isolated, marked narrowing of the left coronary ostia. During surgery, a circumferential aortotomy allowed the examination of the left coronary ostium which appeared severely stenosed. The coronary tree was otherwise normal. A termino-terminal saphenous vein graft was anastomosed on the left stem and its proximal part was implanted on the ascending aorta. The coronary ostium and the proximal part of the left main stem were excised and the macroscopic examination of the proximal part of the left coronary artery confirmed the diagnosis of severe ostial stenosis. Microscopic examination of the coronary ostium showed a severe intimal thickening without any evident lesion of the media. This intimal thickening consisted of fibrous tissue without extracellular lipid deposit. Microscopic examination of the aorta near the coronary ostium also demonstrated an intimal thickening without any lesion of the media. Coronary ostial stenosis appears to be a rare lesion; its incidence has varied between 0.13 and 2.7% in angiographic studies and there is co-existing disease in multiple coronary vessels in the majority of cases.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

心包异常仍是放射性心脏病最常见的表现,但冠状动脉病变也并不罕见。在本报告中,我们描述了一名50岁女性,在因乳腺癌接受纵隔放疗五年后出现左冠状动脉开口狭窄。患者接受了冠状动脉造影。当左心导管尖端进入左冠状动脉开口时观察到压力下降;因此,仅进行了非选择性冠状动脉造影,显示左冠状动脉开口孤立且明显狭窄。手术中,通过环周主动脉切开术检查左冠状动脉开口,发现其严重狭窄。冠状动脉树其他部分正常。将一段大隐静脉端端吻合于左主干,并将其近端部分植入升主动脉。切除冠状动脉开口及左主干近端部分,对左冠状动脉近端进行大体检查证实为严重开口狭窄。冠状动脉开口的显微镜检查显示内膜严重增厚,中膜无明显病变。这种内膜增厚由纤维组织构成,无细胞外脂质沉积。冠状动脉开口附近主动脉的显微镜检查也显示内膜增厚,中膜无病变。冠状动脉开口狭窄似乎是一种罕见病变;在血管造影研究中,其发生率在0.13%至2.7%之间变化,且大多数病例存在多支冠状动脉并存疾病。(摘要截选至250字)

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