Musiani A, Cernigliaro C, Sansa M, Maselli D, De Gasperis C
Division of Cardiovascular Surgery, Ospedale Maggiore di Novara, Italy.
Eur J Cardiothorac Surg. 1997 Mar;11(3):505-14. doi: 10.1016/s1010-7940(96)01121-9.
Left main coronary artery atresia is a rare coronary anomaly in which there is no left coronary ostium, the proximal left main trunk ends blindly, blood flows from the right coronary artery to the left via small collateral arteries and retrogradely in at least one of the left-sided arteries. Since published case reports are few and rather scattered, no comprehensive information about this uncommon anomaly is available.
A through search for published cases of left main coronary atresia was performed in the major medical journals by electronic (MEDLINE and INTERNET) and hand-scanning.
The authors found 28 cases of left main atresia (including two from their own experience), 15 of which were pediatric; five of these cases had associated cardiac anomalies. While pediatric patients were usually overtly symptomatic early in their life (syncope, dyspnea, sudden death, failure to thrive, infarction, ventricular tachycardia), adult patients began showing symptoms (angina, dyspnea, sudden death) only at an advanced age; associated coronary atherosclerosis seemed to be uncommon, though (2/13 adult patients, 15%). We know of only one asymptomatic patient, a 76-year old lady who had died of unrelated causes; in her case left main atresia was an unforeseen autopsy finding. Four untreated patients had died suddenly; most of the others were highly symptomatic and required surgical therapy, usually as direct coronary artery revascularization via one or more saphenous vein or mammary artery grafts to the left-sided arteries; all revascularized patients were reported to be alive and well; in one pediatric case the left main coronary artery was reconstructed using an aortic wall baffle, with a good result. In contrast, the outcome of patients who did not receive revascularization has been poor.
In light of the favorable results obtained by surgical therapy, the authors endorse prompt coronary artery revascularization for all patients with left main coronary artery atresia.
左冠状动脉闭锁是一种罕见的冠状动脉异常,即不存在左冠状动脉开口,左主干近端呈盲端,血液通过小的侧支动脉从右冠状动脉流向左冠状动脉,并至少在一侧的左冠状动脉中逆行。由于已发表的病例报告很少且相当分散,因此尚无关于这种罕见异常的全面信息。
通过电子检索(MEDLINE和互联网)以及手工检索主要医学期刊,全面查找已发表的左冠状动脉闭锁病例。
作者发现了28例左冠状动脉闭锁病例(包括他们自己经验中的2例),其中15例为儿科患者;这些病例中有5例伴有心脏异常。儿科患者通常在生命早期就有明显症状(晕厥、呼吸困难、猝死、发育不良、梗死、室性心动过速),而成人患者仅在高龄时才开始出现症状(心绞痛、呼吸困难、猝死);不过,相关的冠状动脉粥样硬化似乎并不常见(13例成年患者中有2例,占15%)。我们仅知道一名无症状患者,是一位76岁的女性,死于无关原因;在她的病例中,左冠状动脉闭锁是意外的尸检发现。4例未经治疗的患者突然死亡;其他大多数患者症状严重,需要手术治疗,通常是通过一根或多根大隐静脉或乳内动脉移植到左侧动脉进行直接冠状动脉血运重建;据报道,所有接受血运重建的患者均存活且状况良好;在1例儿科病例中,使用主动脉壁挡板重建了左冠状动脉,效果良好。相比之下,未接受血运重建的患者预后较差。
鉴于手术治疗取得的良好效果,作者支持对所有左冠状动脉闭锁患者迅速进行冠状动脉血运重建。