Cocco G, Tarsi G, Bersigotti G, Sgarbi E
Divisione di Cardiologia, Azienda Ospedaliera, Ospedale San Salvatore, Pesaro.
G Ital Cardiol. 1998 Mar;28(3):303-7.
We report a case of acute myocardial infarction which occurred after administration of a synthetic analog of prostaglandin E2 (PGE2) for the voluntary interruption of pregnancy in a 31-year-old woman who had previously been asymptomatic, with myocardial bridging of the left anterior descending artery. The pathogenesis of the severe ischemia causing myocardial infarction and left ventricle aneurysm is quite unclear. The temporal connection is highly indicative of a causal relationship between the pharmacological effects of a synthetic PGE2 analog and coronary spasm responsible for severe ischemia. The hypothesis of endothelial dysfunction proximal to the intramyocardial artery tract and paradoxical vasoconstriction with platelet activation should be taken into consideration. A possible additional effect seems to be a horizontal coronary steal produced by the administration of PGE2 in the myocardium below the intramyocardial artery tract. It cannot be excluded that pharmacological doses of a synthetic analog of PGE2 may have inverted the vasoactive effects of the substance due to direct stimulation on the delivery of constrictive agonist factors.
我们报告了一例急性心肌梗死病例,该病例发生在一名31岁既往无症状且左前降支存在心肌桥的女性使用前列腺素E2(PGE2)合成类似物进行人工流产之后。导致心肌梗死和左心室动脉瘤的严重缺血的发病机制尚不清楚。时间上的关联强烈表明合成PGE2类似物的药理作用与导致严重缺血的冠状动脉痉挛之间存在因果关系。应考虑心肌内动脉段近端内皮功能障碍以及伴有血小板活化的反常血管收缩这一假说。一种可能的附加效应似乎是在心肌内动脉段下方的心肌中给予PGE2所产生的水平性冠状动脉窃血。不能排除合成PGE2类似物的药理剂量可能由于对收缩性激动因子传递的直接刺激而逆转了该物质的血管活性作用。