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爆发性钙化结节作为急性冠状动脉血栓形成和猝死的潜在机制。

Eruptive Calcified Nodules as a Potential Mechanism of Acute Coronary Thrombosis and Sudden Death.

机构信息

CVPath Institute, Gaithersburg, Maryland, USA.

CVPath Institute, Gaithersburg, Maryland, USA; National Cerebral and Cardiovascular Center, Department of Cardiovascular Medicine, Osaka, Japan.

出版信息

J Am Coll Cardiol. 2021 Apr 6;77(13):1599-1611. doi: 10.1016/j.jacc.2021.02.016.

Abstract

BACKGROUND

Calcified nodule (CN) has a unique plaque morphology, in which an area of nodular calcification causes disruption of the fibrous cap with overlying luminal thrombus. CN is reported to be the least frequent cause of acute coronary thrombosis, and the pathogenesis of CN has not been well studied.

OBJECTIVES

The purpose of this study is to provide a comprehensive morphologic assessment of the CN in addition to providing an evolutionary perspective as to how CN causes acute coronary thrombosis in patients with acute coronary syndromes.

METHODS

A total of 26 consecutive CN lesions from 25 subjects from our autopsy registry were evaluated. Detailed morphometric analysis was performed to understand the plaque characteristics of CN and nodular calcification.

RESULTS

The mean age was 70 years, with a high prevalence of diabetes and chronic kidney disease. CNs were equally distributed between men and women, with 61.5% of CNs found in the right coronary artery (n = 16), mainly within its mid-portion (56%). All CNs demonstrated surface nonocclusive luminal thrombus, consisting of multiple nodular fragments of calcification, protruding and disrupting the overlying fibrous cap, with evidence of endothelial cell loss. The degree of circumferential sheet calcification was significantly less in the culprit section (89° [interquartile range: 54° to 177°]) than in the adjacent proximal (206° [interquartile range: 157° to 269°], p = 0.0034) and distal (240° [interquartile range: 178° to 333°], p = 0.0004) sections. Polarized picrosirius red staining showed the presence of necrotic core calcium at culprit sites of CNs, whereas collagen calcium was more prevalent at the proximal and distal regions of CNs.

CONCLUSIONS

Our study suggests that fibrous cap disruption in CN with overlying thrombosis is initiated through the fragmentation of necrotic core calcifications, which is flanked-proximally and distally-by hard, collagen-rich calcification in coronary arteries, which are susceptible to mechanical stress.

摘要

背景

钙化结节(CN)具有独特的斑块形态,其中一个结节状钙化区域会破坏纤维帽,并导致管腔表面覆盖的血栓。CN 被报道为急性冠状动脉血栓形成的最不常见原因,其发病机制尚未得到很好的研究。

目的

本研究旨在对 CN 进行全面形态评估,并提供一个关于 CN 如何在急性冠状动脉综合征患者中导致急性冠状动脉血栓形成的进化视角。

方法

对来自我们尸检登记处的 25 名患者的 26 个连续 CN 病变进行了评估。进行了详细的形态计量分析,以了解 CN 和结节状钙化的斑块特征。

结果

平均年龄为 70 岁,糖尿病和慢性肾脏病的患病率较高。CN 在男性和女性中的分布比例相等,61.5%的 CN 位于右冠状动脉(n=16),主要位于中段(56%)。所有 CN 均显示表面非闭塞性管腔血栓,由多个结节状钙化碎片组成,突出并破坏了覆盖的纤维帽,并伴有内皮细胞丧失的证据。在罪犯节段,周向片状钙化的程度明显小于邻近的近端(89°[四分位距:54°至 177°])和远端(240°[四分位距:178°至 333°])节段(p=0.0034)。偏光 picrosirius 红染色显示在 CN 的罪犯部位存在坏死核心钙,而在 CN 的近端和远端区域,胶原钙更为常见。

结论

我们的研究表明,CN 表面伴血栓形成的纤维帽破裂是通过坏死核心钙化的碎裂启动的,在冠状动脉中,坏死核心钙化的近端和远端被坚硬的富含胶原的钙化所包围,而这些钙化容易受到机械应力的影响。

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